List of skin conditions
Many conditions affect the human integumentary system—the organ system covering the entire surface of the body and composed of skin, hair, nails, and related muscle and glands. The major function of this system is as a barrier against the external environment. The skin weighs an average of four kilograms, covers an area of two square metres, and is made of three distinct layers: the epidermis, dermis, and subcutaneous tissue. The two main types of human skin are: glabrous skin, the hairless skin on the palms and soles, and hair-bearing skin. Within the latter type, the hairs occur in structures called pilosebaceous units, each with hair follicle, sebaceous gland, and associated arrector pili muscle. In the embryo, the epidermis, hair, and glands form from the ectoderm, which is chemically influenced by the underlying mesoderm that forms the dermis and subcutaneous tissues.
The epidermis is the most superficial layer of skin, a squamous epithelium with several strata: the stratum corneum, stratum lucidum, stratum granulosum, stratum spinosum, and stratum basale. Nourishment is provided to these layers by diffusion from the dermis, since the epidermis is without direct blood supply. The epidermis contains four cell types: keratinocytes, melanocytes, Langerhans cells, and Merkel cells. Of these, keratinocytes are the major component, constituting roughly 95 percent of the epidermis. This stratified squamous epithelium is maintained by cell division within the stratum basale, in which differentiating cells slowly displace outwards through the stratum spinosum to the stratum corneum, where cells are continually shed from the surface. In normal skin, the rate of production equals the rate of loss; about two weeks are needed for a cell to migrate from the basal cell layer to the top of the granular cell layer, and an additional two weeks to cross the stratum corneum.
The dermis is the layer of skin between the epidermis and subcutaneous tissue, and comprises two sections, the papillary dermis and the reticular dermis. The superficial papillary dermis with the overlying rete ridges of the epidermis, between which the two layers interact through the basement membrane zone. Structural components of the dermis are collagen, elastic fibers, and ground substance. Within these components are the pilosebaceous units, arrector pili muscles, and the eccrine and apocrine glands. The dermis contains two vascular networks that run parallel to the skin surface—one superficial and one deep plexus—which are connected by vertical communicating vessels. The function of blood vessels within the dermis is fourfold: to supply nutrition, to regulate temperature, to modulate inflammation, and to participate in wound healing.
The subcutaneous tissue is a layer of fat between the dermis and underlying fascia. This tissue may be further divided into two components, the actual fatty layer, or panniculus adiposus, and a deeper vestigial layer of muscle, the panniculus carnosus. The main cellular component of this tissue is the adipocyte, or fat cell. The structure of this tissue is composed of septal and lobular compartments, which differ in microscopic appearance. Functionally, the subcutaneous fat insulates the body, absorbs trauma, and serves as a reserve energy source.
Conditions of the human integumentary system constitute a broad spectrum of diseases, also known as dermatoses, as well as many nonpathologic states. While only a small number of skin diseases account for most visits to the physician, thousands of skin conditions have been described. Classification of these conditions often presents many nosological challenges, since underlying etiologies and pathogenetics are often not known. Therefore, most current textbooks present a classification based on location, morphology, etiology, and so on. Clinically, the diagnosis of any particular skin condition is made by gathering pertinent information regarding the presenting skin lesion, including the location, symptoms, duration, arrangement, morphology, and color. Diagnosis of many conditions often also requires a skin biopsy which yields histologic information that can be correlated with the clinical presentation and any laboratory data.
Acneiform eruptions
s are caused by changes in the pilosebaceous unit.- Acne aestivalis
- Acne conglobata
- Acne cosmetica
- Acne fulminans
- Acne keloidalis nuchae |alt=Adult forehead with scattered red pimples
- Acne mechanica
- Acne medicamentosa
- Acne miliaris necrotica
- Acne vulgaris
- Acne with facial edema
- Blepharophyma
- Erythrotelangiectatic rosacea
- Excoriated acne
- Glandular rosacea
- Gnathophyma
- Gram-negative rosacea
- Granulomatous facial dermatitis |alt=Adult male with a large, red, bulbous nose
- Granulomatous perioral dermatitis
- Halogen acne
- Hidradenitis suppurativa
- Idiopathic facial aseptic granuloma
- Infantile acne
- Lupoid rosacea
- Lupus miliaris disseminatus faciei
- Metophyma
- Neonatal acne
- Occupational acne
- Oil acne
- Ocular rosacea
- Otophyma
- Periorificial dermatitis
- Persistent edema of rosacea
- Phymatous rosacea
- Pomade acne
- Papulopustular rosacea
- Perifolliculitis capitis abscedens et suffodiens
- Perioral dermatitis
- Periorbital dermatitis
- Pyoderma faciale
- Rhinophyma
- Rosacea
- Rosacea conglobata
- Synovitis–acne–pustulosis–hyperostosis–osteomyelitis syndrome
- Steroid rosacea
- Tar acne
- Tropical acne
Autoinflammatory syndromes
- Blau syndrome |alt=Multiple reddish-brown papules coalescing over the right arm of a boy
- Chronic infantile neurologic cutaneous and articular syndrome
- Familial cold urticaria
- Familial Mediterranean fever
- Hyper-IgD syndrome
- Majeed syndrome
- Muckle–Wells syndrome
- TNF receptor associated periodic syndrome
Chronic blistering
- Adult linear IgA disease
- Bullous pemphigoid
- Bullous lupus erythematosus
- Childhood linear IgA disease
- Cicatricial pemphigoid
- Dermatitis herpetiformis
- Endemic pemphigus
- Epidermolysis bullosa acquisita
- Grover's disease |alt=Adult chest and abdomen with many red skin lesions
- IgA pemphigus
- Intraepidermal neutrophilic IgA dermatosis
- Localized cicatricial pemphigoid
- Paraneoplastic pemphigus
- Pemphigus erythematosus
- Pemphigus foliaceus
- Pemphigus herpetiformis
- Pemphigoid nodularis
- Pemphigus vegetans
- Pemphigus vegetans of Hallopeau
- Pemphigus vegetans of Neumann
- Pemphigus vulgaris
- Vesicular pemphigoid
- Vulvar childhood pemphigoid
Conditions of the mucous membranes
- Acatalasia
- Acquired dyskeratotic leukoplakia
- Actinic cheilitis
- Acute necrotizing ulcerative gingivitis
- Allergic contact cheilitis |alt=Adult tongue with a strikingly black top
- Angina bullosa haemorrhagica
- Angular cheilitis
- Behçet's disease
- Black hairy tongue
- Caviar tongue
- Cheilitis exfoliativa
- Cheilitis glandularis
- Cheilitis granulomatosa
- Cutaneous sinus of dental origin
- Cyclic neutropenia
- Desquamative gingivitis
- Drug-induced ulcer of the lip
- Epidermization of the lip
- Epulis
- Epulis fissuratum
- Eruptive lingual papillitis
- Erythroplakia
- Fissured tongue
- Geographic tongue
- Gingival fibroma
- Gingival hypertrophy
- Hairy leukoplakia
- Intraoral dental sinus
- Linea alba
- Leukoplakia
- Leukoplakia with tylosis and esophageal carcinoma
- Major aphthous ulcer
- Median rhomboid glossitis
- Melanocytic oral lesion
- Melkersson–Rosenthal syndrome
- Morsicatio buccarum
- Mucosal squamous cell carcinoma
- Mucous cyst of the oral mucosa
- Nagayama's spots
- Oral Crohn's disease
- Oral florid papillomatosis
- Oral melanosis
- Osseous choristoma of the tongue
- Peripheral ameloblastoma
- Plasma cell cheilitis
- Plasmoacanthoma
- Proliferative verrucous leukoplakia
- Pyogenic granuloma |alt=A solitary papule of inflamed vascular granulation tissue on the index finger of an adult
- Pyostomatitis vegetans
- Recurrent aphthous stomatitis
- Recurrent intraoral herpes simplex infection
- Smooth tongue
- Stomatitis nicotina
- Torus palatinus
- Trumpeter's wart
- Vestibular papillomatosis
- White sponge nevus
Conditions of the skin appendages
- Acne necrotica
- Acquired generalized hypertrichosis
- Acquired perforating dermatosis
- Acrokeratosis paraneoplastica of Bazex
- Acroosteolysis
- Acute paronychia |alt=Circular coin-sized bare patch on the back of a person's scalp
- Alopecia areata
- Alopecia neoplastica
- Anagen effluvium
- Androgenic alopecia
- Anhidrosis
- Anonychia
- Apparent leukonychia
- Beau's lines
- Blue nails
- Bromidrosis
- Bubble hair deformity
- Central centrifugal cicatricial alopecia
- Chevron nail
- Chromhidrosis
- Chronic paronychia
- Cicatricial alopecia
- Clubbing
- Congenital onychodysplasia of the index fingers
- Disseminate and recurrent infundibulofolliculitis
- Erosive pustular dermatitis of the scalp
- Erythromelanosis follicularis faciei et colli
- Folliculitis decalvans
- Folliculitis nares perforans
- Fox–Fordyce disease
- Frontal fibrosing alopecia
- Generalized congenital hypertrichosis
- Generalized hyperhidrosis
- Graham-Little syndrome
- Granulosis rubra nasi |alt=Big toe with most of the toenail missing; only the nail's root is present
- Green nails
- Gustatory hyperhidrosis
- Hair casts
- Hair follicle nevus
- Hairy palms and soles
- Half and half nails
- Hangnail
- Hapalonychia
- Hematidrosis
- Hirsutism
- Hook nail
- Hot comb alopecia
- Hypertrichosis cubiti
- Hypertrichosis simplex of the scalp
- Intermittent hair–follicle dystrophy
- Keratosis pilaris atrophicans
- Kinking hair
- Koenen's tumor
- Koilonychia
- Kyrle disease
- Leukonychia
- Lichen planopilaris
- Lichen planus of the nails
- Lichen spinulosus
- Lipedematous alopecia
- Localized acquired hypertrichosis
- Localized congenital hypertrichosis
- Longitudinal erythronychia
- Longitudinal melanonychia
- Loose anagen syndrome
- Lupus erythematosus
- Madarosis
- Malalignment of the nail plate
- Male-pattern baldness
- Marie–Unna hereditary hypotrichosis
- Median nail dystrophy
- Mees' lines
- Melanonychia
- Menkes kinky hair syndrome
- Monilethrix
- Muehrcke's nails |alt=Multiple, dystrophic, irregular, shortened fingernails
- Nail–patella syndrome
- Neoplasms of the nailbed
- Nevoid hypertrichosis
- Noncicatricial alopecia
- Onychauxis
- Onychoatrophy
- Onychocryptosis
- Onychogryphosis
- Onycholysis
- Onychomadesis
- Onychomatricoma
- Onychophagia
- Onychophosis
- Onychoptosis defluvium
- Onychorrhexis
- Onychoschizia
- Onychotillomania
- Ophiasis
- Palmoplantar hyperhidrosis
- Parakeratosis pustulosa
- Patterned acquired hypertrichosis
- Perforating folliculitis
- Pili annulati
- Pili bifurcati
- Pili multigemini
- Pili pseudoannulati
- Pili torti
- Pincer nails
- Pityriasis amiantacea
- Platonychia
- Plica neuropathica
- Plummer's nail
- Premature greying of hair
- Prepubertal hypertrichosis
- Pressure alopecia
- Pseudofolliculitis barbae
- Pseudopelade of Brocq
- Psoriatic nails
- Pterygium inversum unguis
- Pterygium unguis
- Purpura of the nail bed
- Racquet nail
- Recurrent palmoplantar hidradenitis
- Red lunulae
- Ross' syndrome
- Rubinstein–Taybi syndrome
- Setleis syndrome
- Shell nail syndrome
- Short anagen syndrome
- Splinter hemorrhage |alt=Small, linear, blue-black areas of discoloration beneath the nail plate of an adult finger
- Spotted lunulae
- Staining of the nail plate
- Stippled nails
- Subungual hematoma
- Telogen effluvium
- Terry's nails
- Traction alopecia
- Traumatic alopecia
- Traumatic anserine folliculosis
- Triangular alopecia
- Trichomegaly
- Trichomycosis axillaris
- Trichorrhexis invaginata
- Trichorrhexis nodosa
- Trichostasis spinulosa
- Tufted folliculitis
- Tumor alopecia
- Twenty-nail dystrophy
- Uncombable hair syndrome
- Wooly hair nevus
- X-linked hypertrichosis
Conditions of the subcutaneous fat
- Acquired generalized lipodystrophy
- Adiposis dolorosa
- Alpha-1 antitrypsin deficiency panniculitis
- Atrophic connective tissue panniculitis
- Barraquer–Simons syndrome
- Benign symmetric lipomatosis
- Centrifugal abdominal lipodystrophy
- Chronic erythema nodosum |alt=Dark area of skin, reminiscent of a bruise, on the inner ankle of an adult
- Cold panniculitis
- Congenital generalized lipodystrophy
- Cytophagic histiocytic panniculitis
- Drug-induced lipodystrophy
- Factitial panniculitis
- Familial partial lipodystrophy
- Gouty panniculitis
- Hemihyperplasia–multiple lipomatosis syndrome
- HIV-associated lipodystrophy
- Involutional lipoatrophy
- Lipoatrophia annularis
- Lipoatrophia semicircularis
- Lipodermatosclerosis
- Lipohypertrophy
- Localized lipodystrophy
- Neutrophilic lobular panniculitis
- Nodular vasculitis
- Non-progressive late-onset linear hemifacial lipoatrophy
- Pancreatic panniculitis
- Poland's syndrome
- Post-steroid panniculitis
- Sclerema neonatorum
- Sclerosing lipogranuloma
- Septal panniculitis
- Subcutaneous fat necrosis of the newborn
- Traumatic panniculitis
- Tumor lysis syndrome
- Weber–Christian disease
Congenital anomalies
- Accessory nail of the fifth toe
- Accessory tragus
- Amniotic band syndrome
- Aplasia cutis congenita
- Arteriovenous fistula
- Benign neonatal hemangiomatosis
- Branchial cyst
- Bronchogenic cyst
- Capillary hemangioma
- Cavernous venous malformation
- Congenital cartilaginous rest of the neck
- Congenital erosive and vesicular dermatosis
- Congenital hypertrophy of the lateral fold of the hallux
- Congenital lip pit
- Congenital malformations of the dermatoglyphs
- Congenital smooth muscle hamartoma
- Cystic lymphatic malformation
- Dermoid cyst
- Diffuse neonatal hemangiomatosis
- Encephalocele
- Focal facial dermal dysplasia
- Hutchinson's teeth
- Hyperkeratotic cutaneous capillary-venous malformation
- Intrauterine epidermal necrosis
- Limb–mammary syndrome
- Lowry–MacLean syndrome
- Macrocheilia
- Macrocystic lymphatic malformation
- Malignant pilomatricoma
- Maternal autoimmune bullous disease
- Median raphe cyst
- Melanotic neuroectodermal tumor of infancy
- Membranous aplasia cutis
- Microcystic lymphatic malformation
- Midline cervical cleft
- Mongolian spot |alt=Several light blue patches of skin distributed over a child's lower back and buttock
- Mulberry molar
- Nager acrofacial dysostosis
- Nasal glioma
- Nasolacrimal duct cyst
- Nevus psiloliparus
- Non-involuting congenital hemangioma
- Omphalomesenteric duct cyst
- PELVIS syndrome
- Pilomatricoma
- Poland anomaly
- Posterior fossa malformations–hemangiomas–arterial anomalies–cardiac defects–eye abnormalities–sternal cleft and supraumbilical raphe syndrome
- Preauricular sinus and cyst
- Rapidly involuting congenital hemangioma
- Rosenthal–Kloepfer syndrome
- Rudimentary supernumerary digit
- SACRAL syndrome
- Sinus pericranii
- Skin dimple
- Superficial lymphatic malformation
- Supernumerary nipple
- Thyroglossal duct cyst
- Verrucous vascular malformation
Connective tissue diseases
- Acute cutaneous lupus erythematosus
- Atrophoderma of Pasini and Pierini
- Calcinosis–Raynaud phenomenon–esophageal dysmotility–sclerodactyly–telangiectasia syndrome
- Chilblain lupus erythematosus
- Childhood dermatomyositis
- Childhood discoid lupus erythematosus
- Childhood systemic lupus erythematosus |alt=A young girl with facial palsy, complete ptosis, and marked atrophy of subcutaneous and bony structures on the left upper side of the face
- Complement deficiency syndromes
- Dermatomyositis
- Ehlers–Danlos syndrome
- Eosinophilia–myalgia syndrome
- Frontal linear scleroderma
- Generalized discoid lupus erythematosus
- Generalized morphea
- Interstitial granulomatous dermatitis
- Juvenile rheumatoid arthritis
- Keloid morphea
- Linear atrophoderma of Moulin
- Linear scleroderma
- Localized discoid lupus erythematosus
- Localized morphea
- Lupus erythematosus panniculitis
- Lupus erythematosus–lichen planus overlap syndrome
- Methotrexate-induced papular eruption
- Mixed connective tissue disease
- Morphea profunda
- Morphea–lichen sclerosus et atrophicus overlap
- Mouth and genital ulcers with inflamed cartilage syndrome
- Neonatal lupus erythematosus
- Nephrogenic systemic fibrosis
- Nicolau–Balus syndrome |alt=The lower back of an adult with thickened, indurated patches of skin
- Nodulosis–arthropathy–osteolysis syndrome
- Normophosphatemic familial tumoral calcinosis
- Palisaded neutrophilic and granulomatous dermatitis
- Pansclerotic morphea
- Parry–Romberg syndrome
- Progressive systemic sclerosis
- Relapsing polychondritis
- Rheumatoid arthritis
- Rheumatoid nodulosis
- Rheumatoid vasculitis
- Rowell's syndrome
- Scleredema adultorum
- Silicosis
- Sjögren's syndrome
- Subacute cutaneous lupus erythematosus
- Systemic lupus erythematosus
- Toxic oil syndrome
- Tumid lupus erythematosus
- Tuzun syndrome
- Verrucous lupus erythematosus
- Winchester syndrome
Abnormalities of dermal fibrous and elastic tissue
|alt=Fuzzy red lines on an abdomen
- Acrodermatitis chronica atrophicans
- Actinic elastosis
- Anetoderma
- Blepharochalasis
- Cutis laxa
- Cutis rhomboidalis nuchae
- Ehlers–Danlos syndrome
- Elastosis perforans serpiginosa
- Homocystinuria
- Jadassohn–Pellizzari anetoderma
- Linear focal elastosis
- Loeys–Dietz syndrome
- Marfan syndrome
- Occipital horn syndrome
- Osteogenesis imperfecta
- Perforating calcific elastosis
- Pseudoxanthoma elasticum
- Reactive perforating collagenosis
- Schweninger–Buzzi anetoderma
- Sclerotic fibroma
- Striae atrophicans
- Striae distensae
- Ullrich disease
- Verrucous perforating collagenoma
- Wrinkly skin syndrome
Dermal and subcutaneous growths
- Acquired progressive lymphangioma
- Acral arteriolar ectasia
- Acral fibrokeratoma
- Acrochordon
- Adenoma sebaceum
- Adult type of generalized eruption of cutaneous mastocytosis
- African cutaneous Kaposi sarcoma |alt=Multiple, small, blue to red papules on the scrotum
- African lymphadenopathic Kaposi sarcoma
- Aggressive infantile fibromatosis
- AIDS-associated Kaposi sarcoma
- Ainhum
- Angiofibroma
- Angiokeratoma
- Angiokeratoma of Fordyce
- Angiokeratoma of Mibelli
- Angioleiomyoma
- Angiolipoleiomyoma
- Angiolipoma
- Angioma serpiginosum
- Angiosarcoma
- Aponeurotic fibroma
- Atypical fibroxanthoma
- Benign lipoblastomatosis
- Buschke–Ollendorff syndrome
- Capillary aneurysms
- Carcinoid
- Cherry angioma
- Chondrodermatitis nodularis chronica helicis |alt=Solitary, pink, dome-shaped papule on the superior helix of an adult
- Chondroid lipoma
- Chordoma
- Classic Kaposi sarcoma
- Collagenous fibroma
- Composite hemangioendothelioma
- Connective tissue nevus
- Cutaneous endometriosis
- Cutaneous meningioma
- Cutaneous myelofibrosis
- Cutaneous myxoma
- Cutis marmorata telangiectatica congenita
- Dermal dendrocyte hamartoma
- Dermatofibroma
- Dermatofibrosarcoma protuberans
- Desmoid tumor
- Diffuse cutaneous mastocytosis
- Diffuse infantile fibromatosis
- Dupuytren's contracture
- Eccrine angiomatous hamartoma
- Elastofibroma dorsi
- Endovascular papillary angioendothelioma
- Epithelioid cell histiocytoma
- Epithelioid hemangioendothelioma
- Epithelioid sarcoma
- Erythrodermic mastocytosis
- Extraskeletal chondroma
- Familial myxovascular fibromas
- Fascial hernia
- Fibroma of tendon sheath
- Fibromatosis colli
- Fibrous hamartoma of infancy
- Fibrous papule of the nose
- Folded skin with scarring
- Fordyce's spot
- Ganglion cyst
- Ganglioneuroma
- Genital leiomyoma
- Giant cell fibroblastoma
- Giant cell tumor of the tendon sheath
- Glomeruloid hemangioma |alt=Small, raised, skin-colored lesions
- Glomus tumor
- Granular cell tumor
- Hamartoma
- Hemangiopericytoma
- Hemangiosarcoma
- Hibernoma
- Hypertrophic scar
- Immunosuppression-associated Kaposi sarcoma
- Infantile digital fibromatosis
- Infantile hemangiopericytoma
- Infantile myofibromatosis
- Infantile systemic hyalinosis
- Intradermal spindle cell lipoma
- Intravascular papillary endothelial hyperplasia
- Juvenile hyaline fibromatosis
- Kaposiform hemangioendothelioma
- Kasabach–Merritt syndrome
- Keloid |alt=Excessive scar tissue along an adult jawline
- Keratinizing metaplasia
- Keratocyst
- Klippel–Trenaunay syndrome
- Knuckle pads
- Leiomyosarcoma
- Lipoma
- Liposarcoma
- Lymphangiectasis
- Lymphangiomatosis
- Malignant fibrous histiocytoma
- Malignant peripheral nerve sheath tumor
- Mast cell sarcoma
- Meningocele
- Metastatic carcinoma
- Microvenular hemangioma
- Midline nevus flammeus
- Multifocal lymphangioendotheliomatosis
- Multinucleate cell angiohistocytoma
- Multiple cutaneous and uterine leiomyomatosis syndrome
- Multiple cutaneous leiomyoma
- Neural fibrolipoma
- Neuroblastoma
- Neuroma cutis
- Neurothekeoma
- Nevus flammeus
- Nevus flammeus nuchae
- Nevus lipomatosus superficialis
- Nevus oligemicus |alt=A small blue- to purple-colored lesion on the lower lip of an adult
- Nodular fasciitis
- Oral submucous fibrosis
- Pachydermodactyly
- Palisaded encapsulated neuroma
- Paraneoplastic syndrome
- Pearly penile papules
- Peyronie's disease
- Phakomatosis pigmentovascularis
- Piloleiomyoma
- Plantar fibromatosis
- Pleomorphic fibroma
- Pleomorphic lipoma
- Plexiform fibrohistiocytic tumor
- Porokeratotic eccrine ostial and dermal duct nevus
- Progressive nodular histiocytoma
- Proliferating angioendotheliomatosis
- Prominent inferior labial artery
- Pseudo-ainhum
- Retiform hemangioendothelioma
- Schwannoma
- Solitary angiokeratoma
- Solitary cutaneous leiomyoma
- Solitary mastocytoma |alt=Multiple tan patches scattered over the back of a young child
- Solitary neurofibroma
- Spider angioma
- Spindle cell hemangioendothelioma
- Spindle cell lipoma
- Sternal cleft
- Subungual exostosis
- Superficial acral fibromyxoma
- Systemic mastocytosis
- Targetoid hemosiderotic hemangioma
- Telangiectasia
- Telangiectasia macularis eruptiva perstans
- Teratoma
- Tufted angioma
- Umbilical granuloma
- Universal angiomatosis
- Urticaria pigmentosa
- Venous lake
- Wildervanck syndrome
- Xanthelasmoidal mastocytosis
- Zosteriform metastasis
Dermatitis
- Childhood granulomatous periorificial dermatitis
- Essential dermatitis
Atopic
- Atopic dermatitis
Contact
- Abietic acid dermatitis
- Acid-induced
- Acrylic monomer dermatitis
- Adhesive dermatitis
- African blackwood dermatitis
- Airbag dermatitis
- Alkali-induced
- Allergic
- Antifungal agent-induced
- Antimicrobial agent-induced
- Arsenic dermatitis
- Artificial nail-induced
- Axillary antiperspirant-induced
- Axillary deodorant-induced
- Baboon syndrome
- Black dermatographism
- Bleaching cream-induced
- Capsaisin-induced
- Chemical burn |alt=Red erosions, some with crusting, all on the back of an adult hand
- Chloracne
- Chrome dermatitis
- Clothing-induced
- Cobalt dermatitis
- Contact stomatitis
- Contact urticaria
- Corticosteroid-induced
- Cosmetic dermatitis
- Cosmetic intolerance syndrome
- Dentifrice-induced
- Dermatitis from metals and metal salts
- Dust-induced
- Epoxy resin dermatitis
- Ethylenediamine-induced
- Eye makeup-induced
- Fiberglass dermatitis
- Flower-induced
- Formaldehyde-induced
- Formaldehyde-releasing agent-induced
- Fragrance-induced
- Gold dermatitis
- Hair bleach-induced
- Hair dye-induced
- Hair lotion-induced
- Hair spray-induced
- Hair straightener-induced
- Hair tonic-induced
- Houseplant-induced
- Hydrocarbon-induced
- Irritant folliculitis
- Lacquer dermatitis
- Lanolin-induced
- Lipstick-induced
- Local anesthetic-induced
- Makassar ebony dermatitis
- Marine plant-induced
- Mechanical irritant dermatitis
- Mercury dermatitis
- Mouthwash-induced
- Nail lacquer-induced
- Nail polish remover-induced
- Nickel dermatitis
- Occupation-induced
- p-Chloro-meta-xylenol-induced
- Paraben-induced
- Paraphenylenediamine dermatitis
- Permanent wave preparation-induced
- Phenothiazine drug-induced
- Photoallergic
- Photoirritant
- Plant derivative-induced
- Pollen-induced
- Polyester resin dermatitis
- Propylene glycol-induced |alt=Blisters distributed over an adult forearm
- Protein contact dermatitis
- Quaternium-15 hypersensitivity
- Reed dermatitis
- Rosewood dermatitis
- Rosin dermatitis
- Rubber dermatitis
- Seed-induced
- Shoe dermatitis
- Solvent-induced
- Sorbic acid-induced
- Subjective irritant contact dermatitis
- Sunscreen-induced
- Systemic contact dermatitis
- Tear gas dermatitis
- Textile dermatitis
- Traumatic irritant contact dermatitis
- Tree-associated plant-induced
- Tree-induced
- Tulip fingers
- Urshiol-induced
- Vegetable-induced
Eczema
|alt=Small blisters and crusting on the distal fingertips
- Autoimmune estrogen dermatitis
- Autoimmune progesterone dermatitis
- Autosensitization dermatitis
- Breast eczema
- Chronic vesiculobullous hand eczema
- Circumostomy eczema
- Dyshidrosis
- Ear eczema
- Eyelid dermatitis
- Hand eczema
- Hyperkeratotic hand dermatitis
- Id reaction
- Irritant diaper dermatitis
- Juvenile plantar dermatosis
- Molluscum dermatitis
- Nummular dermatitis
- Nutritional deficiency eczema
- Sulzberger–Garbe syndrome
- Xerotic eczema
Pustular
- Eosinophilic pustular folliculitis
- Reactive arthritis
- Subcorneal pustular dermatosis
Seborrheic
- Infantile seborrheic dermatitis
- Leiner's disease
- Pityriasis simplex capillitii
- Seborrheic dermatitis
Disturbances of pigmentation
- Albinism–black lock–cell migration disorder of the neurocytes of the gut–deafness syndrome
- Albinism–deafness syndrome
- Alezzandrini syndrome
- Argyria
- Arsenic poisoning |alt=Depigmented patches on the posterior hand and fingers
- Berlin syndrome
- Canthaxanthin
- Chédiak–Higashi syndrome
- Chrysiasis
- Cross–McKusick–Breen syndrome
- Dermatopathia pigmentosa reticularis
- Dyschromatosis symmetrica hereditaria
- Dyschromatosis universalis hereditaria
- Elejalde syndrome
- Familial progressive hyperpigmentation
- Galli–Galli disease
- Griscelli syndrome type 2
- Griscelli syndrome type 3
- Hemochromatosis
- Hemosiderin hyperpigmentation
- Hermansky–Pudlak syndrome
- Idiopathic guttate hypomelanosis
- Iron metallic discoloration
- Klein–Waardenburg syndrome
- Lead poisoning
- Leukoderma
- Melanoma-associated leukoderma
- Melasma
- Mukamel syndrome
- Necklace of Venus
- Nevus anemicus |alt=Multiple, hypopigmented macules and patches on the leg of an adult
- Nevus depigmentosus
- Ocular albinism
- Oculocutaneous albinism
- Pallister–Killian syndrome
- Periorbital hyperpigmentation
- Photoleukomelanodermatitis of Kobori
- Phylloid hypomelanosis
- Piebaldism
- Pigmentatio reticularis faciei et colli
- Pityriasis alba
- Poikiloderma of Civatte
- Poikiloderma vasculare atrophicans
- Postinflammatory hyperpigmentation
- Postinflammatory hypopigmentation
- Progressive macular hypomelanosis
- Quadrichrome vitiligo
- Reticular pigmented anomaly of the flexures
- Reticulate acropigmentation of Kitamura
- Revesz syndrome
- Riehl melanosis
- Scratch dermatitis
- Segmental vitiligo
- Shah–Waardenburg syndrome
- Shiitake mushroom dermatitis
- Tar melanosis
- Tietz syndrome
- Titanium metallic discoloration
- Transient neonatal pustular melanosis
- Trichrome vitiligo
- Vagabond's leukomelanoderma
- Vasospastic macule
- Vitiligo
- Vitiligo ponctué
- Vogt–Koyanagi–Harada syndrome
- Waardenburg syndrome
- Wende–Bauckus syndrome
- Woronoff's ring
- X-linked reticulate pigmentary disorder
- Yemenite deaf-blind hypopigmentation syndrome
Drug eruptions
- Acrodynia
- Acute generalized exanthematous pustulosis |alt=Multiple small subcorneal pustules on erythematous patches
- Adverse reaction to biologic agents
- Adverse reaction to cytokines
- Allopurinol hypersensitivity syndrome
- Anticoagulant-induced skin necrosis
- Anticonvulsant hypersensitivity syndrome
- Bromoderma
- Bullous drug reaction
- Chemotherapy-induced acral erythema
- Chemotherapy-induced hyperpigmentation
- Drug-induced acne
- Drug-induced angioedema
- Drug-related gingival hyperplasia
- Drug-induced lichenoid reaction
- Drug-induced lupus erythematosus
- Drug-induced nail changes
- Drug-induced pigmentation
- Drug-induced pseudolymphoma
- Drug-induced urticaria
- Erythema multiforme major
- Exudative hyponychial dermatitis
- Fixed drug reaction
- Halogenoderma
- Heparin necrosis
- HIV disease-related drug reaction
- Hydroxyurea dermopathy
- Injection site reaction
- Iododerma
- Leukotriene receptor antagonist-associated Churg–Strauss syndrome
- Linear IgA bullous dermatosis
- Photosensitive drug reaction
- Red man syndrome
- Severe cutaneous adverse reactions
- Scleroderma-like reaction to taxanes
- Serum sickness-like reaction
- Steroid acne
- Steroid folliculitis
- Stevens–Johnson syndrome
- Sulfonamide hypersensitivity syndrome
- Texier's disease
- Toxic epidermal necrolysis
- Urticarial erythema multiforme
- Vitamin K reaction
- Warfarin necrosis
Endocrine-related
- Acanthosis nigricans associated with malignancy
- Acanthosis nigricans associated with obesity, insulin-resistant states, and endocrinopathy
- Acral acanthosis nigricans |alt=Blackened necrosis of multiple toes on an adult foot
- Acral dry gangrene
- Acromegaly
- Addison's disease
- Adrenal adenoma
- Adrenal carcinoma
- Adrenal hyperplasia
- Alopecia–nail dystrophy–ophthalmic complications–thyroid dysfunction–hypohidrosis–ephelides and enteropathy–respiratory tract infections syndrome
- Arrhenoblastoma
- Cretinism
- Cushing's syndrome |alt=Hyperpigmented plaque with velvety textural change within the axillary fold of an adult
- Excess ovarian androgen release syndrome
- Familial acanthosis nigricans
- Growth hormone deficiency
- Hyperandrogenism–insulin resistance–acanthosis nigricans syndrome
- Hyperparathyroidism
- Hyperprolactinemic SAHA syndrome
- Hyperthyroidism
- Hypoparathyroidism
- Hypothyroidism
- Leydig cell tumor
- Multiple endocrine neoplasia type 1
- Multiple endocrine neoplasia type 2
- Multiple endocrine neoplasia type 3
- Myxedema
- Panhypopituitarism
- Persistent adrenarche syndrome
- Polycystic ovarian syndrome
- Seborrhoea–acne–hirsutism–alopecia
- Thyroid acropachy
Eosinophilic
- Angiolymphoid hyperplasia with eosinophilia
- Annular erythema of infancy
- Arthropod assault
- Eosinophilic cellulitis
- Eosinophilic fasciitis
- Eosinophilic granuloma
- Eosinophilic granulomatosis with polyangiitis
- Eosinophilic pustular folliculitis of infancy
- Eosinophilic ulcer of the oral mucosa |alt=Solitary, large, white to yellow erosion on the inner lower lip of a child
- Eosinophilic vasculitis
- Erythema toxicum neonatorum
- Granuloma faciale
- Hypereosinophilia
- Hypereosinophilic syndrome
- Incontinentia pigmenti
- Itchy red bump disease
- Juvenile xanthogranuloma
- Kimura's disease
- Nodules–eosinophilia–rheumatism–dermatitis–swelling syndrome
- Pachydermatous eosinophilic dermatitis
- Papular eruption of blacks
- Papuloerythroderma of Ofuji
- Pruritic papular eruption of HIV disease
Epidermal nevi, neoplasms, and cysts
- Aberrant basal cell carcinoma
- Acanthoma fissuratum
- Acrospiroma
- Actinic keratosis
- Adenoid squamous cell carcinoma
- Aggressive digital papillary adenocarcinoma |alt=Solitary, pink, pearly appearing skin lesion on the side of an adult nose
- Apocrine gland carcinoma
- Apocrine nevus
- Arsenical keratosis
- Atrophic actinic keratosis
- Balanitis plasmacellularis
- Basal cell carcinoma
- Basaloid follicular hamartoma
- Basaloid squamous cell carcinoma
- Birt–Hogg–Dubé syndrome
- Bowen's disease
- Brooke–Fordyce syndrome
- Ceruminoma
- Cicatricial basal cell carcinoma
- Ciliated cyst of the vulva
- Clear cell acanthoma
- Clear cell squamous cell carcinoma
- Chronic scar keratosis
- Clonal seborrheic keratosis
- Common seborrheic keratosis
- Cowden syndrome
- Cutaneous ciliated cyst
- Cutaneous columnar cyst
- Cutaneous horn
- Cystic basal cell carcinoma
- Dermal eccrine cylindroma
- Dermatosis papulosa nigra
- Desmoplastic trichoepithelioma
- Dilated pore |alt=Two coalescing, red, scaly patches on the dorsal surface of an adult finger
- Eccrine carcinoma
- Eccrine nevus
- Epidermal cyst
- Epidermal nevus syndrome
- Epidermolytic acanthoma
- Epithelioma cuniculatum
- Eruptive vellus hair cyst
- Erythroplasia of Queyrat
- Extramammary Paget's disease
- Fibroepithelioma
- Fibroepithelioma of Pinkus
- Fibrofolliculoma
- Follicular hybrid cyst
- Folliculosebaceous-apocrine hamartoma
- Folliculosebaceous cystic hamartoma
- Generalized eruptive keratoacanthoma
- Giant solitary trichoepithelioma
- Hidradenoma |alt=Large, red, exophytic nodule on the malar surface of an adult
- Hidradenocarcinoma
- Hidrocystoma
- Hydrocarbon keratosis
- Hyperkeratosis lenticularis perstans
- Hyperkeratosis of the nipple and areola
- Hyperkeratotic actinic keratosis
- Ichthyosis hystrix
- Ichthyosis hystrix of Curth–Macklin
- Infiltrative basal cell carcinoma
- Inflammatory linear verrucous epidermal nevus
- Inverted follicular keratosis
- Irritated seborrheic keratosis
- Isthmicoma
- Juvenile myelomonocytic leukemia
- Keratin implantation cyst
- Keratoacanthoma
- Keratoacanthoma centrifugum marginatum
- Large cell acanthoma
- Lichenoid actinic keratosis
- Lichenoid keratosis
- Linear verrucous epidermal nevus
- Malignant acrospiroma
- Malignant mixed tumor
- Malignant trichilemmal cyst
- Mantleoma
- Marjolin's ulcer
- Melanoacanthoma
- Merkel cell carcinoma
- Microcystic adnexal carcinoma
- Micronodular basal cell carcinoma
- Milia en plaque
- Milium
- Mixed tumor
- Mucinous carcinoma
- Mucinous nevus
- Muir–Torre syndrome
- Multiple familial trichoepithelioma
- Multiple keratoacanthomas
- Multiple minute digitate hyperkeratosis
- Nevoid basal cell carcinoma syndrome
- Nevus comedonicus
- Nevus comedonicus syndrome
- Nevus sebaceous
- Nevus unius lateris
- Nodular basal cell carcinoma
- Paget's disease of the breast
- Papillary eccrine adenoma
- Papillary hidradenoma
- Papillomatosis cutis carcinoides
- Patch blue nevus
- Perifollicular fibroma
- Phakomatosis pigmentokeratotica
- Pigmented actinic keratosis
- Pigmented basal cell carcinoma
- Pigmented hairy epidermal nevus syndrome
- Pilar sheath acanthoma
- Pilonidal sinus
- Polypoid basal cell carcinoma
- Pore-like basal cell carcinoma
- Primary cutaneous adenoid cystic carcinoma
- Proliferating epidermoid cyst
- Proliferating trichilemmal cyst
- Pseudocyst of the auricle
- Pseudoepitheliomatous keratotic and micaceous balanitis
- PUVA keratosis
- Rasmussen syndrome
- Reactional keratosis
- Reticulated seborrheic keratosis
- Rodent ulcer
- Schimmelpenning syndrome
- Sebaceoma
- Sebaceous adenoma
- Sebaceous carcinoma
- Sebaceous hyperplasia
- Sebaceous nevus syndrome
- Seboacanthoma
- Seborrheic keratosis
- Seborrheic keratosis with squamous atypia
- Signet-ring cell squamous cell carcinoma
- Solitary keratoacanthoma
- Solitary trichoepithelioma
- Spindle cell squamous cell carcinoma
- Spiradenoma
- Squamous cell carcinoma |alt=Ulceration and crusting over a skin lesion on the front of an adult nose
- Steatocystoma multiplex
- Steatocystoma simplex
- Stucco keratosis
- Superficial basal cell carcinoma
- Syringadenoma papilliferum
- Syringofibroadenoma
- Syringoma
- Systematized epidermal nevus
- Thermal keratosis
- Trichilemmal carcinoma
- Trichilemmal cyst
- Trichilemmoma
- Trichoadenoma
- Trichoblastoma
- Trichoblastic fibroma
- Trichodiscoma
- Trichofolliculoma
- Unilateral palmoplantar verrucous nevus
- Urethral caruncle
- Verrucous carcinoma
- Verrucous cyst
- Viral keratosis
- Warty dyskeratoma
- Waxy keratosis of childhood
- Zoon's vulvitis
- Zosteriform speckled lentiginous nevus
Erythemas
- Erythema annulare centrifugum
- Erythema gyratum repens
- Erythema migrans
- Erythema multiforme
- Erythema multiforme minor
- Erythema palmare
- Generalized erythema
- Necrolytic acral erythema
- Necrolytic migratory erythema
Genodermatoses
- 18q deletion syndrome
- Acrodermatitis enteropathica
- Acrogeria
- Acrokeratosis verruciformis
- Adams–Oliver syndrome
- Adducted thumbs syndrome
- Albright's hereditary osteodystrophy
- Angelman syndrome
- Apert syndrome
- Arthrogryposis–renal dysfunction–cholestasis syndrome
- Ataxia telangiectasia
- Atrichia with papular lesions
- Atrophodermia vermiculata
- Autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy syndrome
- Bart syndrome
- Bazex–Dupré–Christol syndrome
- Beare–Stevenson cutis gyrata syndrome
- Bloom syndrome
- Blue rubber bleb nevus syndrome
- Brittle hair–intellectual impairment–decreased fertility–short stature syndrome
- Cantú syndrome
- Cardio-facio-cutaneous syndrome
- Cartilage–hair hypoplasia
- Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome
- Childhood tumor syndrome
- Chondrodysplasia punctata
- Cicatricial junctional epidermolysis bullosa
- Craniosynostosis–anal anomalies–porokeratosis syndrome
- Cockayne syndrome
- Colobomas of the eye–heart defects–ichthyosiform dermatosis–mental retardation–ear defects syndrome
- Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome
- Conradi–Hünermann syndrome
- Costello syndrome
- Cronkhite–Canada syndrome
- Crouzon syndrome
- Cutis verticis gyrata
- Darier's disease |alt=Many hyperkeratotic, vegetative, and hyperpigmented papules in a zosteriform pattern on the right lateral lower extremity of an adult
- DeSanctis–Cacchione syndrome
- Disseminated superficial actinic porokeratosis
- Disseminated superficial porokeratosis
- Dolichol kinase deficiency
- Dominant dystrophic epidermolysis bullosa
- Dyskeratosis congenita
- Dystrophic epidermolysis bullosa
- Ectodermal dysplasia
- Ectodermal dysplasia with corkscrew hairs
- Ectrodactyly–ectodermal dysplasia–cleft syndrome
- Epidermolysis bullosa herpetiformis
- Epidermolysis bullosa simplex
- Epidermolysis bullosa simplex of Ogna
- Epidermolysis bullosa simplex with mottled pigmentation
- Epidermolysis bullosa simplex with muscular dystrophy
- Epidermolytic hyperkeratosis
- Erythrokeratodermia with ataxia
- Familial benign chronic pemphigus
- Fanconi syndrome
- Fibrodysplasia ossificans progressiva
- Focal dermal hypoplasia
- Follicular atrophoderma
- Franceschetti–Klein syndrome
- Gardner's syndrome
- Gastrocutaneous syndrome
- Generalized atrophic benign epidermolysis bullosa
- Generalized epidermolysis bullosa simplex
- Generalized trichoepithelioma
- Giant axonal neuropathy with curly hair
- Gingival fibromatosis with hypertrichosis
- Haber syndrome
- Hallerman–Streiff syndrome
- Harlequin-type ichthyosis
- Hay–Wells syndrome
- Hereditary sclerosing poikiloderma |alt=Small, red, monomorphic skin lesions on the back of an adult arm
- Heterochromia iridum
- Holocarboxylase synthetase deficiency
- Hypohidrotic ectodermal dysplasia
- Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome
- Hypotrichosis–lymphedema–telangiectasia syndrome
- Ichthyosis–brittle hair–impaired intelligence–decreased fertility–short stature syndrome
- Ichthyosis bullosa of Siemens
- Ichthyosis follicularis
- Ichthyosis linearis circumflexa
- Ichthyosis prematurity syndrome
- Ichthyosis vulgaris
- Ichthyosis with confetti
- Neonatal ichthyosis–sclerosing cholangitis syndrome
- Incontinentia pigmenti achromians
- Immune dysfunction–polyendocrinopathy–enteropathy–X-linked syndrome
- Jaffe–Campanacci syndrome
- Johanson–Blizzard syndrome
- Johnson–McMillin syndrome
- Joubert syndrome
- Junctional epidermolysis bullosa
- Junctional epidermolysis bullosa gravis
- Junctional epidermolysis bullosa with pyloric atresia
- Kabuki syndrome
- Keratolytic winter erythema
- Keratosis follicularis spinulosa decalvans
- Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
- Keratosis pilaris atrophicans faciei
- Keratosis pilaris
- Kindler syndrome
- Klinefelter syndrome
- Klippel–Feil syndrome
- Lamellar ichthyosis
- Legius syndrome
- Lelis syndrome
- Lenz–Majewski syndrome
- Leschke syndrome
- Lethal acantholytic epidermolysis bullosa
- Lhermitte–Duclos disease
- Linear and whorled nevoid hypermelanosis
- Linear Darier disease
- Linear porokeratosis
- Localized epidermolysis bullosa simplex
- Mandibuloacral dysplasia
- Marinesco–Sjögren syndrome
- McCune–Albright syndrome
- McCusick syndrome
- Metageria
- Microphthalmia–dermal aplasia–sclerocornea syndrome
- Mitis junctional epidermolysis bullosa
- Mitochondrial myopathy–encephalopathy–lactic acidosis–stroke syndrome
- Multiple lentigines syndrome
- Multiple pterygium syndrome
- Multiple sulfatase deficiency
- Naegeli–Franceschetti–Jadassohn syndrome
- Netherton syndrome
- Neurofibromatosis type 1 |alt=Many small to large, skin colored nodules on the trunk of an adult
- Neurofibromatosis type 3
- Neurofibromatosis type 4
- Neutral lipid storage disease
- Nonbullous congenital ichthyosiform erythroderma
- Noonan syndrome
- Oculocerebrocutaneous syndrome
- Oculodentodigital dysplasia
- Odonto–Tricho–Ungual–Digital–Palmar syndrome
- Oliver–McFarlane syndrome
- Orofaciodigital syndrome
- Pachydermoperiostosis
- Peeling skin syndrome
- Pfeiffer syndrome
- Photosensitivity–ichthyosis–brittle sulfur-deficient hair–impaired intelligence–decreased fertility–short stature syndrome
- Pityriasis rotunda
- Plate-like osteoma cutis
- Plaque-type porokeratosis
- Polyneuropathy–organomegaly–endocrinopathy–monoclonal gammopathy–skin changes syndrome
- Polyostotic fibrous dysplasia
- Popliteal pterygium syndrome
- Porokeratosis
- Porokeratosis palmaris et plantaris disseminata
- Prader–Willi syndrome
- Progeria
- Progressive osseous heteroplasia
- Progressive symmetric erythrokeratodermia
- Proteus syndrome
- Proteus-like syndrome
- Punctate porokeratosis
- Rapp–Hodgkin syndrome
- Recessive dystrophic epidermolysis bullosa
- Refsum's disease
- Relapsing linear acantholytic dermatosis
- Restrictive dermopathy |alt=Thick, fish-like scales on an adult lower leg
- Rhizomelic chondrodysplasia punctata
- Rombo syndrome
- Rothmund–Thomson syndrome
- Rud syndrome
- Say syndrome
- Scalp–ear–nipple syndrome
- Schindler disease
- Schinzel–Giedion syndrome
- Scleroatrophic syndrome of Huriez
- Segmental neurofibromatosis
- Senter syndrome
- Shabbir syndrome
- Silver–Russell syndrome
- Sjögren–Larsson syndrome
- Skin fragility syndrome
- Smith–Lemli–Opitz syndrome
- Sturge–Weber syndrome
- Supernumerary nipples–uropathies–Becker's nevus syndrome
- Terminal osseous dysplasia with pigmentary defects
- Tooth and nail syndrome
- Townes–Brocks syndrome
- Transient bullous dermolysis of the newborn |alt=Frontal image of a child's face showing large hyperkeratotic papules and plaques with some induration suspicious for actinic keratoses and early squamous cell carcinomas
- Treacher Collins syndrome
- Tricho–dento–osseous syndrome
- Tricho–rhino–phalangeal syndrome
- Tuberous sclerosis
- Turner syndrome
- Ulnar–mammary syndrome
- Van Der Woude syndrome
- Von Hippel–Lindau syndrome
- Watson syndrome
- Werner syndrome
- Westerhof syndrome
- Whistling syndrome
- Wilson–Turner syndrome
- Wolf–Hirschhorn syndrome
- X-linked ichthyosis
- X-linked recessive chondrodysplasia punctata
- Xeroderma pigmentosum
- XXYY genotype
- Zimmermann–Laband syndrome
Infection-related
Bacterium-related
Bacterium-related cutaneous conditions often have distinct morphologic characteristics that may be an indication of a generalized systemic process or simply an isolated superficial infection.- Aeromonas infection
- African tick bite fever
- American tick bite fever
- Arcanobacterium haemolyticum infection
- Bacillary angiomatosis
- Bejel
- Blastomycosis-like pyoderma
- Blistering distal dactylitis
- Botryomycosis
- Brill–Zinsser disease
- Brucellosis
- Bubonic plague
- Bullous impetigo
- Cat scratch disease
- Cellulitis |alt=Redness and mild swelling of an adult leg
- Chancre
- Chancroid
- Chlamydial infection
- Chronic lymphangitis
- Chronic recurrent erysipelas
- Chronic undermining burrowing ulcers
- Chromobacteriosis infection
- Condylomata lata
- Cutaneous actinomycosis
- Cutaneous anthrax infection
- Cutaneous C. diphtheriae infection
- Cutaneous group B streptococcal infection
- Cutaneous Pasteurella hemolytica infection
- Cutaneous Streptococcus iniae infection
- Dermatitis gangrenosa
- Ecthyma
- Ecthyma gangrenosum
- Ehrlichiosis ewingii infection
- Elephantiasis nostras
- Endemic typhus
- Epidemic typhus
- Erysipelas
- Erysipeloid of Rosenbach
- Erythema marginatum
- Erythrasma
- External otitis |alt=Exudate over a background of redness on the external ear canal of an adult
- Felon
- Flea-borne spotted fever
- Flinders Island spotted fever
- Flying squirrel typhus
- Folliculitis
- Fournier gangrene
- Furunculosis
- Gas gangrene
- Glanders
- Gonococcemia
- Gonorrhea
- Gram-negative folliculitis
- Gram-negative toe web infection
- Granuloma inguinale
- Green nail syndrome
- Group JK Corynebacterium sepsis
- Haemophilus influenzae cellulitis
- Helicobacter cellulitis
- Hospital furunculosis
- Hot tub folliculitis
- Human granulocytotropic anaplasmosis
- Human monocytotropic ehrlichiosis
- Impetigo contagiosa
- Japanese spotted fever
- Leptospirosis
- Listeriosis
- Ludwig's angina
- Lupoid sycosis
- Lyme disease
- Lymphogranuloma venereum
- Malakoplakia
- Mediterranean spotted fever
- Melioidosis
- Meningococcemia
- Missouri Lyme disease
- Mycoplasma infection
- Necrotizing fasciitis
- Neonatal toxic shock-like exanthematous disease
- Nocardiosis
- Noma neonatorum
- North Asian tick typhus
- Ophthalmia neonatorum |alt=Redness and swelling of an ear
- Oroya fever
- Pasteurellosis
- Perianal cellulitis
- Periapical abscess
- Pinta
- Pitted keratolysis
- Plague
- Primary gonococcal dermatitis
- Pseudomonal pyoderma
- Pseudomonas hot-foot syndrome
- Pyogenic paronychia
- Pyomyositis
- Q fever
- Queensland tick typhus
- Rat-bite fever
- Recurrent toxin-mediated perineal erythema
- Rhinoscleroma
- Rickettsia aeschlimannii infection
- Rickettsialpox
- Rocky Mountain spotted fever
- Saber shin
- Saddle nose
- Salmonellosis
- Scarlet fever
- Scrub typhus
- Shigellosis
- Staphylococcal scalded skin syndrome
- Streptococcal intertrigo
- Superficial pustular folliculitis
- Sycosis vulgaris
- Syphilid
- Syphilis
- Tick-borne lymphadenopathy
- Toxic shock syndrome
- Trench fever
- Tropical ulcer
- Tularemia
- Verruga peruana
- Vibrio vulnificus infection
- Yaws
''Mycobacterium''-related
- Aquarium granuloma
- Borderline lepromatous leprosy
- Borderline leprosy
- Borderline tuberculoid leprosy
- Buruli ulcer |alt=Ulceration of the skin over the back of a teenager's hand
- Erythema induratum
- Histoid leprosy
- Lepromatous leprosy
- Leprosy
- Lichen scrofulosorum
- Lupus vulgaris
- Miliary tuberculosis
- Mycobacterium avium-intracellulare complex infection
- Mycobacterium haemophilum infection
- Mycobacterium kansasii infection
- Papulonecrotic tuberculid
- Primary inoculation tuberculosis
- Rapid-growing Mycobacterium infection
- Scrofuloderma
- Tuberculosis cutis orificialis
- Tuberculosis verrucosa cutis
- Tuberculous cellulitis
- Tuberculous gumma
- Tuberculoid leprosy
Mycosis-related
- African histoplasmosis
- Alternariosis
- Antibiotic candidiasis
- Black piedra
- Candidal intertrigo
- Candidal onychomycosis
- Candidal paronychia
- Candidal vulvovaginitis
- Candidid
- Chromoblastomycosis
- Chronic mucocutaneous candidiasis
- Coccidioidomycosis
- Congenital cutaneous candidiasis
- Cryptococcosis
- Dermatophytid
- Diaper candidiasis
- Disseminated coccidioidomycosis
- Distal subungual onychomycosis
- Entomophthoromycosis
- Erosio interdigitalis blastomycetica |alt=A large brown colored plaque on the top of a child's head
- Favus
- Fungal folliculitis
- Fusariosis
- Geotrichosis
- Granuloma gluteale infantum
- Histoplasmosis
- Hyalohyphomycosis
- Kerion
- Lobomycosis
- Mucormycosis
- Mycetoma
- North American blastomycosis
- Onychomycosis
- Oral candidiasis
- Otomycosis
- Perianal candidiasis
- Perlèche
- Phaeohyphomycosis
- Piedra
- Pityrosporum folliculitis
- Primary cutaneous aspergillosis
- Primary cutaneous coccidioidomycosis
- Primary cutaneous histoplasmosis
- Primary pulmonary coccidioidomycosis
- Primary pulmonary histoplasmosis
- Progressive disseminated histoplasmosis
- Proximal subungual onychomycosis
- Rhinosporidiosis
- South American blastomycosis
- Sporotrichosis
- Systemic candidiasis
- Tinea barbae |alt=Multiple circular, red, scaling lesions on a male cheek
- Tinea capitis
- Tinea corporis
- Tinea corporis gladiatorum
- Tinea cruris
- Tinea faciei
- Tinea imbricata
- Tinea incognito
- Tinea manuum
- Tinea nigra
- Tinea pedis
- Tinea versicolor
- White piedra
- White superficial onychomycosis
- Zygomycosis
Parasitic infestations, stings, and bites
- Acanthamoeba infection
- Amebiasis cutis
- Ant sting
- Arachnidism
- Baker's itch
- Balamuthia infection
- Bedbug infestation
- Bee and wasp stings
- Blister beetle dermatitis
- Bombardier beetle burn
- Bristleworm sting |alt=Multiple, red, linear plaques on the extremity
- Centipede bite
- Cheyletiella dermatitis
- Chigger bite
- Coolie itch
- Copra itch
- Coral dermatitis
- Creeping eruption
- Cutaneous leishmaniasis
- Cysticercosis cutis
- Demodex mite bite
- Dogger Bank itch
- Dracunculiasis
- Echinococcosis
- Elephantiasis tropica
- Elephant skin
- Enterobiasis
- Erisipela de la costa
- Feather pillow dermatitis
- Funnel web spider bite
- Gamasoidosis
- Gnathostomiasis
- Grain itch
- Grocer's itch
- Head lice infestation
- Hookworm disease
- Human trypanosomiasis
- Hydroid dermatitis
- Irukandji syndrome
- Jellyfish dermatitis
- Ked itch
- Larva currens
- Latrodectism
- Leech bite
- Leopard skin
- Lepidopterism
- Lizard skin
- Loaiasis
- Loxoscelism
- Mal morando
- Millipede burn
- Mosquito bite
- Mucocutaneous leishmaniasis
- Myiasis
- Nairobi fly dermatitis
- Nematode dermatitis
- Norwegian scabies |alt=Diffuse thickening of the skin over an adult's bilateral arms and fingers
- Onchocerciasis
- Ophthalmia nodosa
- Paederus dermatitis
- Pediculosis corporis
- Pediculosis pubis
- Pneumocystosis
- Portuguese man-of-war dermatitis
- Post-kala-azar dermal leishmaniasis
- Protothecosis
- Pulicosis
- Reduviid bite
- Scabies
- Scorpion sting
- Sea anemone dermatitis
- Seabather's eruption
- Sea urchin injury
- Seaweed dermatitis
- Snake bite
- Sowda
- Sparganosis
- Spider bite
- Stingray injury
- Swimmer's itch |alt=Multiple red bumps on the lower legs and feet
- Tarantula bite
- Tick bite
- Toxoplasmosis
- Trichinosis
- Trichomoniasis
- Tungiasis
- Visceral leishmaniasis
- Visceral schistosomiasis
- Viscerotropic leishmaniasis
- Wheat warehouse itch
Virus-related
- Alphavirus infection
- Asymmetric periflexural exanthem of childhood
- B virus infection
- Boston exanthem disease
- Bovine papular stomatitis
- Bowenoid papulosis
- Buffalopox
- Butcher's wart
- Chikungunya fever
- Condylomata acuminata
- Congenital rubella syndrome
- Cowpox
- Cytomegalic inclusion disease
- Dengue
- Disseminated herpes zoster
- Eczema herpeticum |alt=A diffuse, generalized red rash over a newborn's entire body
- Eczema vaccinatum
- Epidermodysplasia verruciformis
- Eruptive pseudoangiomatosis
- Erythema infectiosum
- Exanthem of primary HIV infection
- Farmyard pox
- Generalized vaccinia
- Genital herpes
- Gianotti–Crosti syndrome
- Giant condyloma acuminatum
- Hand-foot-and-mouth disease
- Heck's disease
- Hemorrhagic fever with renal syndrome
- Hepatitis B
- Hepatitis C
- Herpangina
- Herpes gladiatorum
- Herpes simplex
- Herpes zoster oticus
- Herpetic keratoconjunctivitis
- Herpetic sycosis
- Herpetic whitlow
- HIV-associated pruritus
- Human monkeypox
- Human T-lymphotropic virus 1 infection
- Human tanapox
- Immune reconstitution inflammatory syndrome
- Infectious mononucleosis
- Inflammatory skin lesions following zoster infection
- Intrauterine herpes simplex |alt=Multiple dark red skin lesions
- Kaposi sarcoma
- Lassa fever
- Lipschütz ulcer
- Measles
- Milker's nodule
- Modified varicella-like syndrome
- Molluscum contagiosum
- Myrmecia
- Neonatal herpes simplex
- Ophthalmic zoster
- Orf
- Orf-induced immunobullous disease
- Orolabial herpes
- Papular purpuric gloves and socks syndrome
- Pigmented wart
- Postherpetic neuralgia
- Post-vaccination follicular eruption
- Progressive vaccinia
- Pseudocowpox
- Recurrent respiratory papillomatosis |alt=Multiple red papules scattered over a child's head, neck, trunk, and upper extremities
- Rift Valley fever
- Roseola infantum
- Roseola vaccinia
- Rubella
- Sandfly fever
- Sealpox
- Varicella
- Variola major
- Verruca plana
- Verruca plantaris
- Verruca vulgaris
- Verrucae palmares et plantares
- Viral-associated trichodysplasia
- Wasting syndrome
- West Nile virus infection
- Zoster
- Zoster sine herpete
Lichenoid eruptions
- Annular lichen planus |alt=Violaceous, annular, scaly plaques on the face and scalp of an adult
- Atrophic lichen planus
- Bullous lichen planus
- Erosive lichen planus
- Erythema dyschromicum perstans
- Giant cell lichenoid dermatitis
- Hepatitis-associated lichen planus
- Hypertrophic lichen planus
- Idiopathic eruptive macular pigmentation
- Inverse lichen planus
- Keratosis lichenoides chronica
- Kraurosis vulvae
- Lichen nitidus
- Lichen planus actinicus
- Lichen planus pemphigoides
- Lichen planus pigmentosus
- Lichen planus–lichen sclerosus overlap syndrome
- Lichen ruber moniliformis
- Lichen sclerosus
- Lichen striatus
- Lichen verrucosus et reticularis
- Lichenoid trikeratosis
- Lichenoid dermatitis
- Lichenoid reaction of graft-versus-host disease
- Linear lichen planus
- Mucosal lichen planus
- Peno-gingival syndrome
- Ulcerative lichen planus
- Vulvovaginal gingival syndrome
- Vulvovaginal lichen planus
Lymphoid-related
- Adult T-cell leukemia/lymphoma
- Angiocentric lymphoma
- Angioimmunoblastic T-cell lymphoma
- Blastic NK-cell lymphoma
- CD30+ cutaneous T-cell lymphoma
- Cutaneous lymphoid hyperplasia |alt=A solitary, large, red papule on the left cheek of an adult male
- Cutaneous lymphoid hyperplasia with bandlike and perivascular patterns
- Cutaneous lymphoid hyperplasia with nodular pattern
- Diffuse large B-cell lymphoma
- Granulocytic sarcoma
- Granulomatous slack skin
- Hairy-cell leukemia
- Hodgkin's disease
- Ichthyosis acquisita
- IgG4-related skin disease
- Intravascular large B-cell lymphoma
- Jessner lymphocytic infiltrate of the skin
- Kikuchi's disease
- Large plaque parapsoriasis
- Lennert lymphoma
- Leukemia cutis
- Lymphoma cutis
- Lymphomatoid granulomatosis
- Lymphomatoid papulosis
- Malignant histiocytosis
- Marginal zone B-cell lymphoma
- Mucosa-associated lymphoid tissue lymphoma
- Mycosis fungoides
- Non-mycosis fungoides CD30− cutaneous large T-cell lymphoma
- Nonspecific cutaneous conditions associated with leukemia
- Pagetoid reticulosis
- Pityriasis lichenoides chronica
- Pityriasis lichenoides et varioliformis acuta
- Plasmacytoma |alt=A large ulcerated plaque on the leg of an adult male
- Plasmacytosis
- Pleomorphic T-cell lymphoma
- Polycythemia vera
- Primary cutaneous follicular lymphoma
- Primary cutaneous immunocytoma
- Primary cutaneous marginal zone lymphoma
- Retiform parapsoriasis
- Secondary cutaneous CD30+ large cell lymphoma
- Sézary syndrome
- Sinus histiocytosis with massive lymphadenopathy
- Subcutaneous T-cell lymphoma
- Vesiculopustular eruption and leukemoid reaction in Down syndrome
Melanocytic nevi and neoplasms
- Acral nevus
- Amelanotic blue nevus |alt=A large, light-tan colored patch of skin over an adult's left shoulder and upper back
- Balloon cell nevus
- Bannayan–Riley–Ruvalcaba syndrome
- Becker's nevus
- Benign melanocytic nevus
- Blue nevus
- Blue nevus of Jadassohn–Tièche
- Carney complex
- Cellular blue nevus
- Centrofacial lentiginosis
- Congenital melanocytic nevus
- Deep penetrating nevus
- Dysplastic nevus
- Dysplastic nevus syndrome
- Ephelis
- Epithelioid blue nevus
- Generalized lentiginosis
- Giant pigmented nevus
- Halo nevus
- Hori's nevus
- Inherited patterned lentiginosis in black persons
- Ink spot lentigo
- Laugier–Hunziker syndrome
- Lentigo simplex
- Malignant blue nevus
- Medium-sized congenital nevocytic nevus
- Melanoacanthoma
- Melanocytic tumors of uncertain malignant potential
- Moynahan syndrome
- Mucosal lentigines
- Nevus of Ito
- Nevus of Ota
- Nevus spilus
- Partial unilateral lentiginosis
- Peutz–Jeghers syndrome
- Pigmented spindle cell nevus
- Pseudomelanoma
- PUVA lentigines
- Small-sized congenital nevocytic nevus
- Spitz nevus
- Solar lentigo
Melanoma
- Acral lentiginous melanoma |alt=A dark brown to black, irregularly shaped nodule on the malar surface of an adult
- Amelanotic melanoma
- Animal-type melanoma
- Desmoplastic melanoma
- Lentigo maligna
- Lentigo maligna melanoma
- Melanoma with features of a Spitz nevus
- Melanoma with small nevus-like cells
- Mucosal melanoma
- Nevoid melanoma
- Nodular melanoma
- Polypoid melanoma
- Seborrheic keratosis-like melanoma
- Soft-tissue melanoma
- Superficial spreading melanoma
- Uveal melanoma
Monocyte- and macrophage-related
- Actinic granuloma
- Annular elastolytic giant cell granuloma
- Annular sarcoidosis |alt=Large, well demarcated plaques with red, active borders, all located on the lower leg of an adult
- Benign cephalic histiocytosis
- Congenital self-healing reticulohistiocytosis
- Erythrodermic sarcoidosis
- Generalized eruptive histiocytoma
- Generalized granuloma annulare
- Giant cell reticulohistiocytoma
- Granuloma annulare in HIV disease
- Granuloma multiforme
- Hand–Schüller–Christian disease
- Heerfordt's syndrome
- Hereditary progressive mucinous histiocytosis
- Hypopigmented sarcoidosis
- Ichthyosiform sarcoidosis
- Indeterminate cell histiocytosis
- Interstitial granulomatous drug reaction
- Langerhans cell histiocytosis
- Letterer–Siwe disease
- Localized granuloma annulare
- Löfgren syndrome
- Lupus pernio
- Morpheaform sarcoidosis
- Mucosal sarcoidosis
- Multicentric reticulohistiocytosis
- Necrobiotic xanthogranuloma
- Non-X histiocytosis
- Papular sarcoid
- Papular xanthoma
- Patch-type granuloma annulare
- Perforating granuloma annulare |alt=Multiple reddish-brownish papules and plaques on the left mandibular region of an adult face
- Progressive nodular histiocytosis
- Reticulohistiocytoma
- Scar sarcoid
- Sea-blue histiocytosis
- Subcutaneous granuloma annulare
- Subcutaneous sarcoidosis
- Systemic sarcoidosis
- Ulcerative sarcoidosis
- Xanthoma disseminatum
Mucinoses
- Acral persistent papular mucinosis
- Atypical lichen myxedematosus
- Atypical tuberous myxedema
- Cutaneous focal mucinosis
- Cutaneous lupus mucinosis
- Discrete papular lichen myxedematosus
- Eccrine mucinosis
- Follicular mucinosis
- Localized lichen myxedematosus
- Myxoid cyst
- Myxoid lipoblastoma
- Neuropathia mucinosa cutanea
- Nodular lichen myxedematosus
- Papular mucinosis
- Papular mucinosis of infancy
- Perifollicular mucinosis
- Reticular erythematous mucinosis
- Scleroderma
- Self-healing juvenile cutaneous mucinosis
- Self-healing papular mucinosis
- Stiff skin syndrome
Neurocutaneous
- Atypical chronic pain syndrome
- Body dysmorphic disorder
- Brachioradial pruritus
- Bromidrosiphobia
- Complex regional pain syndrome
- Congenital insensitivity to pain with anhidrosis
- Delusional parasitosis
- Dermatothlasia
- Factitious dermatitis |alt=Multiple, well-demarcated, linear, longitudinal erosions on the dorsum of the bilateral forearms
- Glossodynia
- Levator ani syndrome
- Malum perforans pedis
- Meralgia paresthetica
- Neurotic excoriations
- Notalgia paresthetica
- Postencephalitic trophic ulcer
- Psychogenic pruritus
- Riley–Day syndrome
- Scalp dysesthesia
- Sciatic nerve injury
- Scrotodynia
- Syringomyelia
- Traumatic neuroma
- Trichotillomania
- Trigeminal neuralgia
- Trigeminal trophic lesion
- Vulvodynia
Noninfectious immunodeficiency-related
- Bare lymphocyte syndrome
- Chronic granulomatous disease
- Common variable immunodeficiency
- Complement deficiency
- DiGeorge syndrome
- Graft-versus-host disease
- Griscelli syndrome
- Hyper-IgE syndrome
- Immunodeficiency with hyper-IgM
- Immunodeficiency–centromeric instability–facial anomalies syndrome
- Isolated IgA deficiency
- Isolated primary IgM deficiency
- Janus kinase 3 deficiency
- Leukocyte adhesion molecule deficiency
- LIG4 syndrome
- Myeloperoxidase deficiency
- Neutrophil immunodeficiency syndrome
- Nezelof syndrome
- Omenn syndrome |alt=Redness and scaliness of the entire skin on a 5-month-old female infant
- Purine nucleoside phosphorylase deficiency
- Severe combined immunodeficiency
- Shwachman–Bodian–Diamond syndrome
- Thymoma with immunodeficiency
- Transient hypogammaglobulinemia of infancy
- Warts–hypogammaglobulinemia–infections–myelokathexis syndrome
- Wiskott–Aldrich syndrome
- X-linked agammaglobulinemia
- X-linked hyper-IgM syndrome
- X-linked hypogammaglobulinemia
- X-linked lymphoproliferative disease
- X-linked neutropenia
Nutrition-related
- Biotin deficiency
- Carotenemia
- Essential fatty acid deficiency
- Folic acid deficiency
- Hypervitaminosis A
- Hypovitaminosis A
- Iron deficiency |alt=Small, scattered bumps on a child's lower back and buttock
- Kwashiorkor
- Lycopenemia
- Maple syrup urine disease
- Marasmus
- Niacin deficiency
- Selenium deficiency
- Vitamin B1 deficiency
- Vitamin B12 deficiency
- Vitamin B2 deficiency
- Vitamin B6 deficiency
- Vitamin B6 excess
- Vitamin C deficiency
- Vitamin K deficiency
- Zinc deficiency
Papulosquamous hyperkeratotic
|alt=Multiple, red, well demarcated papules and plaques on the flank of an adult male
- Confluent and reticulated papillomatosis
- Digitate dermatosis
- Drug-induced keratoderma
- Exfoliative dermatitis
- Florid cutaneous papillomatosis
- Granular parakeratosis
- Keratolysis exfoliativa
- Keratosis punctata of the palmar creases
- Meesmann corneal dystrophy
- Paraneoplastic keratoderma
- Pityriasis rosea
- Pityriasis rubra pilaris
- Pure hair-nail type ectodermal dysplasia
- Small plaque parapsoriasis
- Tripe palms
- Xanthoerythrodermia perstans
Palmoplantar keratodermas
|alt=Bottom of an adult's foot with a thickened and scaling surface
- Acrokeratoelastoidosis of Costa
- Aquagenic keratoderma
- Bart–Pumphrey syndrome
- Camisa disease
- Carvajal syndrome
- Corneodermatoosseous syndrome
- Diffuse epidermolytic palmoplantar keratoderma
- Diffuse nonepidermolytic palmoplantar keratoderma
- Erythrokeratodermia variabilis
- Focal acral hyperkeratosis
- Focal palmoplantar and gingival keratosis
- Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
- Haim–Munk syndrome
- Hidrotic ectodermal dysplasia
- Howel–Evans syndrome
- Hystrix-like ichthyosis–deafness syndrome
- Keratoderma climactericum
- Keratosis punctata palmaris et plantaris
- Keratitis–ichthyosis–deafness syndrome
- Mal de Meleda
- Naxos syndrome
- Olmsted syndrome
- Pachyonychia congenita type I
- Pachyonychia congenita type II
- Palmoplantar keratoderma and spastic paraplegia
- Palmoplantar keratoderma of Sybert
- Papillon–Lefèvre syndrome
- Porokeratosis plantaris discreta
- Punctate palmoplantar keratoderma
- Schöpf–Schulz–Passarge syndrome
- Scleroatrophic syndrome of Huriez
- Striate palmoplantar keratoderma
- Spiny keratoderma
- Tyrosinemia type II
- Vohwinkel syndrome
Pregnancy-related
- Impetigo herpetiformis
- Intrahepatic cholestasis of pregnancy
- Linea nigra
- Pemphigoid gestationis
- Prurigo gestationis
- Pruritic folliculitis of pregnancy
- Pruritic urticarial papules and plaques of pregnancy
- Striae gravidarum
Pruritic
- Adult blaschkitis
- Aquadynia
- Aquagenic pruritus
- Biliary pruritus
- Cholestatic pruritus
- Drug-induced pruritus
- Hydroxyethyl starch-induced pruritus
- Lichen simplex chronicus |alt=Large, hyperpigmented, lichenified plaque
- Prion pruritus
- Prurigo nodularis
- Prurigo pigmentosa
- Prurigo simplex
- Pruritus ani
- Pruritus scroti
- Pruritus vulvae
- Puncta pruritica
- Scalp pruritus
- Senile pruritus
- Uremic pruritus
Psoriasis
|alt=Large, red, scaly plaque
- Annular pustular psoriasis
- Drug-induced psoriasis
- Exanthematic pustular psoriasis
- Generalized pustular psoriasis
- Guttate psoriasis
- Inverse psoriasis
- Keratoderma blennorrhagica
- Localized pustular psoriasis
- Napkin psoriasis
- Psoriasis vulgaris
- Psoriatic arthritis
- Psoriatic erythroderma
- Seborrheic-like psoriasis
Reactive neutrophilic
|alt=Multiple ulcerations with undermined edges on the adult back and upper, posterior arm
- Acute erythema nodosum
- Bowel-associated dermatosis–arthritis syndrome
- Marshall syndrome
- Neutrophilic dermatosis of the dorsal hands
- Neutrophilic eccrine hidradenitis
- Pyoderma gangrenosum
- Pyogenic arthritis–pyoderma gangrenosum–acne syndrome
- Rheumatoid neutrophilic dermatitis
- Superficial granulomatous pyoderma
- Sweet's syndrome
- Sweet's syndrome-like dermatosis
- Vesicopustular dermatosis
Recalcitrant palmoplantar eruptions
- Dermatitis repens
- Infantile acropustulosis
- Palmoplantar pustulosis
- Pustular bacterid
Resulting from errors in metabolism
- Acute intermittent porphyria
- Adrenoleukodystrophy
- Alkaptonuria
- Aminolevulinic acid dehydratase deficiency porphyria
- B-mannosidase deficiency
- Carotenosis
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome
- Cerebrotendinous xanthomatosis
- Citrullinemia
- Congenital erythropoietic porphyria
- Diabetic bulla
- Diabetic cheiroarthropathy
- Diabetic dermopathy
- Dystrophic calcinosis cutis
- Eruptive xanthoma
- Erythropoietic protoporphyria |alt=The skin of an adult face that is thickening with a waxy or leathery appearance, also with areas of hyperkeratosis
- Fabry disease
- Familial alpha-lipoprotein deficiency
- Familial amyloid polyneuropathy
- Familial apoprotein CII deficiency
- Familial combined hyperlipidemia
- Familial defective apolipoprotein B-100
- Familial dysbetalipoproteinemia
- Familial hypertriglyceridemia
- Farber disease
- Fucosidosis
- Gaucher's disease
- Gout
- Hartnup disease
- Hemodialysis-associated amyloidosis
- Hepatoerythropoietic porphyria
- Hereditary coproporphyria
- Hereditary gelsolin amyloidosis
- Heredofamilial amyloidosis
- Hunter syndrome
- Hurler syndrome
- Hurler–Scheie syndrome
- Hyaluronidase deficiency
- Iatrogenic calcinosis cutis
- Idiopathic scrotal calcinosis
- Lafora disease
- Lesch–Nyhan syndrome
- Lichen amyloidosis
- Limited joint mobility
- Lipoid proteinosis
- Lipoprotein lipase deficiency
- Macular amyloidosis |alt=Multiple nodules on the hands of an adult
- Maroteaux–Lamy syndrome
- Medication-induced hyperlipoproteinemia
- Metastatic calcinosis cutis
- Milia-like calcinosis
- Morquio's disease
- Necrobiosis lipoidica
- Niemann–Pick disease
- Nodular amyloidosis
- Nodular xanthoma
- Normolipoproteinemic xanthomatosis
- Obstructive liver disease
- Ochronosis
- Osteoma cutis
- Palmar xanthoma
- Phenylketonuria
- Phytosterolemia
- Porphyria cutanea tarda
- Primary cutaneous amyloidosis
- Primary systemic amyloidosis
- Prolidase deficiency
- Pseudoporphyria
- Sanfilippo syndrome
- Scheie syndrome
- Secondary cutaneous amyloidosis
- Secondary systemic amyloidosis
- Sialidosis
- Sly syndrome
- Subepidermal calcified nodule
- Transient erythroporphyria of infancy |alt=Multiple broad yellow papules around the medial canthi bilaterally in an adult
- Traumatic calcinosis cutis
- Tuberoeruptive xanthoma
- Tumoral calcinosis
- Variegate porphyria
- Verruciform xanthoma
- Waxy skin
- Wilson's disease
- Xanthelasma palpebrarum
- Xanthoma diabeticorum
- Xanthoma planum
- Xanthoma striatum palmare
- Xanthoma tendinosum
- Xanthoma tuberosum
Resulting from physical factors
- Abrasion
- Acrocyanosis
- Actinic prurigo
- Aerosol burn
- Benign summer light eruption
- Beryllium granuloma
- Black heel and palm
- Callus
- Carbon stain |alt=Redness and swelling of the distal toes
- Chilblains
- Chronic actinic dermatitis
- Colloid milium
- Coma blister
- Coral cut
- Delayed blister
- Dermatosis neglecta
- Edema blister
- Electrical burn
- Equestrian perniosis
- Erythema ab igne
- Erythrocyanosis crurum
- Favre–Racouchot syndrome
- Foreign body reaction
- Fracture blister
- Friction blister
- Frostbite
- Garrod's pad
- Harpist's finger
- Heel stick wound
- Heat edema
- Hot tar burn
- Hunan hand syndrome
- Hydroa vacciniforme
- Jogger's nipple
- Juvenile spring eruption
- Kairo cancer
- Kang cancer
- Kangri ulcer
- Lightning burn
- Loop mark
- Magnetic resonance imaging burn
- Mercury granuloma
- Miliaria crystallina
- Miliaria profunda
- Miliaria pustulosa
- Miliaria rubra
- Narcotic dermopathy
- Occlusion miliaria
- Painful fat herniation
- Peat fire cancer
- Photoaging
- Photosensitivity with HIV infection
- Phototoxic tar dermatitis
- Photosenitization
- Phytophotodermatitis
- Pinch mark
- Polymorphous light eruption
- Postmiliarial hypohidrosis |alt=A large ulceration of the lower back with complete loss of the overlying skin
- Postoperative hematoma
- Pressure ulcer
- Pseudoacanthosis nigricans
- Pseudoverrucous papules and nodules
- Pulling boat hands
- PUVA-induced acrobullous dermatosis
- Runner's rump
- Sclerosing lymphangiitis
- Silica granuloma
- Silicone granuloma
- Skin pop scar
- Skin track
- Slap mark
- Solar erythema
- Soot tattoo
- Subcutaneous emphysema
- Sucking blister
- Sunburn
- Surfer's knots
- Tattoo
- Tennis toe
- Thermal burn
- Traumatic asphyxia
- Trench foot
- Tropical anhidrotic asthenia
- Tropical immersion foot
- Turf toe
- Uranium dermatosis
- UV-sensitive syndrome
- Vibration white finger
- Warm water immersion foot
- Weathering nodule of ear
- Wrestler's ear
- Zirconium granuloma
Ionizing radiation-induced
- Acute radiodermatitis |alt=Large red patches of skin on the back and arm from multiple prolonged electrophysiological and ablation procedures with bi-plane fluoroscopy
- Chronic radiation keratosis
- Chronic radiodermatitis
- Eosinophilic, polymorphic, and pruritic eruption associated with radiotherapy
- Fluoroscopy burn
- Radiation acne
- Radiation cancer
- Radiation dermatitis
- Radiation recall reaction
- Radiation-induced erythema multiforme
- Radiation-induced hypertrophic scar
- Radiation-induced keloid
- Radiation-induced morphea
Urticaria and angioedema
urticaria, is characterized by a well-defined, edematous swelling that involves subcutaneous tissues, abdominal organs, or upper airway.
|alt=Raised, edematous, red skin lesions on the abdomen
- Acquired C1 esterase inhibitor deficiency
- Acute urticaria
- Adrenergic urticaria
- Anaphylaxis
- Aquagenic urticaria
- Cholinergic urticaria
- Chronic urticaria
- Cold urticaria
- Dermatographism
- Episodic angioedema with eosinophilia
- Exercise urticaria
- Galvanic urticaria
- Heat urticaria
- Hereditary angioedema
- Localized heat contact urticaria
- Mast cell-independent urticaria
- Physical urticaria
- Primary cold contact urticaria
- Pressure urticaria
- Reflex cold urticaria
- Schnitzler syndrome
- Secondary cold contact urticaria
- Solar urticaria
- Systemic capillary leak syndrome
- Urticarial allergic eruption
- Urticaria-like follicular mucinosis
- Vibratory angioedema
Vascular-related
- Aagenaes syndrome
- Acroangiodermatitis
- Acute hemorrhagic edema of infancy
- Arterial insufficiency ulcer
- Arteriosclerosis obliterans
- Bier spots
- Blueberry muffin baby
- Bonnet–Dechaume–Blanc syndrome
- Bullous lymphedema
- Bullous small vessel vasculitis
- Calciphylaxis |alt=Multiple purpura and early necrosis of skin
- Caput succedaneum
- Cholesterol embolus
- Cobb syndrome
- Corona phlebectatica
- Cryofibrinogenemic purpura
- Cryoglobulinemic purpura
- Cryoglobulinemic vasculitis
- Cutaneous small-vessel vasculitis
- Deep venous thrombosis
- Disseminated intravascular coagulation
- Doucas and Kapetanakis pigmented purpura
- Drug-induced purpura
- Drug-induced thrombocytopenic purpura
- Eczematid-like purpura of Doucas and Kapetanakis
- Epidemic dropsy
- Erythema elevatum diutinum
- Erythromelalgia
- Factitial lymphedema
- Fibrinolysis syndrome
- Food-induced purpura
- Generalized essential telangiectasia
- Giant-cell arteritis
- Gougerot–Blum syndrome
- Granulomatosis with polyangiitis
- Harlequin color change
- Hematopoietic ulcer
- Hennekam syndrome
- Henoch–Schönlein purpura |alt=Red, non-blanching skin lesions on the upper leg
- Hereditary hemorrhagic telangiectasia
- Idiopathic thrombocytopenic purpura
- IgA vasculitis
- Kawasaki's disease
- Levamisole-induced vasculitis
- Lichen aureus
- Livedo racemosa
- Livedo reticularis
- Livedoid dermatitis
- Livedoid vasculopathy
- Lymphedema praecox
- Lymphedema–distichiasis syndrome
- Maffucci syndrome
- Majocchi's disease
- Malignant atrophic papulosis
- Marshall–White syndrome
- Meige lymphedema
- Microscopic polyangiitis
- Mondor's disease
- Neuropathic ulcer
- Njolstad syndrome
- Nonne–Milroy–Meige syndrome
- Obstructive purpura
- Orthostatic purpura
- Painful bruising syndrome
- Parkes Weber syndrome
- Paroxysmal hand hematoma
- Paroxysmal nocturnal hemoglobinuria
- Polyarteritis nodosa
- Postcardiotomy syndrome
- Perinatal gangrene of the buttock
- Pigmentary purpuric eruptions
- Postinflammatory lymphedema
- Postmastectomy lymphangiosarcoma
- Purpura fulminans
- Purpura secondary to clotting disorders
- Purpuric agave dermatitis |alt=White and red discoloration of the distal fingertips
- Raynaud phenomenon
- Raynaud's disease
- Reactive angioendotheliomatosis
- Schamberg's disease
- Secondary lymphedema
- Septic thrombophlebitis
- Sinusoidal hemangioma
- Sneddon's syndrome
- Solar purpura
- Stasis dermatitis
- Superficial thrombophlebitis
- Takayasu arteritis
- Temporal arteritis
- Thromboangiitis obliterans
- Thrombotic thrombocytopenic purpura
- Traumatic purpura
- Trousseau's syndrome
- Unilateral nevoid telangiectasia
- Urticarial vasculitis
- Venous insufficiency ulceration
- Waldenström hyperglobulinemic purpura
- Waldenström macroglobulinemia
- Yellow nail syndrome
Footnotes