Here is the list of all Skin Diseases
- Aagenaes syndrome
- Aarskog syndrome
- Abdominal chemodectomas with cutaneous angiolipomas
- Absence of fingerprints congenital milia
- Acanthosis nigricans – Not a rare disease
- Acquired generalized lipodystrophy
- Acral peeling skin syndrome
- Acrodermatitis
- Acrodermatitis enteropathica
- Acrogeria, Gottron type
- Acrokeratoelastoidosis of Costa
- Actinic lichen planus
- Acute febrile neutrophilic dermatosis
- Acute intermittent porphyria
- Adams-Oliver syndrome
- Adiposis dolorosa
- ADULT syndrome
- Adult T-cell leukemia/lymphoma
- Ainhum
- Al-Gazali-Donnai-Mueller syndrome
- Albinism deafness syndrome
- Alkaptonuria
- Alopecia epilepsy oligophrenia syndrome of Moynahan
- Alopecia totalis
- Alopecia universalis
- Alopecia, epilepsy, pyorrhea, mental subnormality
- Alopecia-contractures-dwarfism-intellectual disability syndrome
- Alopecia-intellectual disability syndrome
- Ambras syndrome
- Ameloonychohypohidrotic syndrome
- Aminolevulinate dehydratase deficiency porphyria
- Amyopathic dermatomyositis
- Angioma serpiginosum
- Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
- Annular atrophic lichen planus
- Annular lichen planus
- Anonychia-onychodystrophy with hypoplasia or absence of distal phalanges
- Antecubital pterygium
- Aplasia cutis congenita
- Aplasia cutis congenita intestinal lymphangiectasia
- Aplasia cutis congenita of limbs recessive
- AREDYLD
- Arterial tortuosity syndrome
- Arthrochalasia Ehlers-Danlos syndrome
- Arthrogryposis and ectodermal dysplasia
- Arthrogryposis renal dysfunction cholestasis syndrome
- Arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay
- Ataxia telangiectasia
- Atrophic lichen planus
- Atrophoderma of Pasini and Pierini
- Atrophoderma vermiculata
- Autosomal dominant deafness-onychodystrophy syndrome
- Autosomal dominant hyper IgE syndrome
- Autosomal dominant palmoplantar keratoderma and congenital alopecia
- Autosomal erythropoietic protoporphyria
- Autosomal recessive candidiasis familial chronic mucocutaneous
- Autosomal recessive palmoplantar keratoderma and congenital alopecia
- Bannayan-Riley-Ruvalcaba syndrome
- Barber Say syndrome
- Barraquer-Simons syndrome
- Basaran Yilmaz syndrome
- Bazex-Dupre-Christol syndrome
- Beare-Stevenson cutis gyrata syndrome
- Becker nevus syndrome
- Becker’s nevus
- Behçet disease
- Benign eccrine spiradenoma
- Biotinidase deficiency
- Birt-Hogg-Dube syndrome
- Bjornstad syndrome
- Blau syndrome
- Blepharo-cheilo-odontic syndrome
- Bloom syndrome
- Blue rubber bleb nevus syndrome
- Book syndrome
- Bork Stender Schmidt syndrome
- Brittle cornea syndrome
- Brunsting-Perry syndrome
- Bullous dystrophy hereditary macular type
- Buschke-Ollendorff syndrome
- Campomelia Cumming type
- Cantu syndrome
- Cardiac-Valvular Ehlers-Danlos syndrome
- Cardiofaciocutaneous syndrome
- Cardiomyopathy dilated with woolly hair and keratoderma
- Carney complex
- Cartilage-hair hypoplasia
- Cerebellar ataxia ectodermal dysplasia
- Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome
- Cerebro-oculo-facio-skeletal syndrome
- Cerebrotendinous xanthomatosis
- Cervical hypertrichosis peripheral neuropathy
- Chanarin-Dorfman syndrome
- Chediak-Higashi syndrome
- Cheilitis glandularis
- CHILD syndrome
- Chorea-acanthocytosis
- Chromhidrosis
- Chromosome 17q11.2 deletion syndrome
- Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature
- Chronic granulomatous disease
- Chronic recurrent multifocal osteomyelitis
- Circumferential skin creases Kunze type
- Classical-like Ehlers-Danlos syndrome
- Clouston syndrome
- CLOVES syndrome
- Cobb syndrome
- Cockayne syndrome type I
- Cockayne syndrome type II
- Cockayne syndrome type III
- COG7-CDG (CDG-IIe)
- Combined immunodeficiency with skin granulomas
- Congenital erythropoietic porphyria
- Congenital generalized lipodystrophy
- Congenital generalized lipodystrophy type 2 – See Congenital generalized lipodystrophy
- Congenital generalized lipodystrophy type 4
- Corneodermatoosseous syndrome
- Corticosteroid-sensitive aseptic abscesses
- Costello syndrome
- Cowden syndrome
- Crandall syndrome
- Cranioectodermal dysplasia
- Cronkhite-Canada disease
- Cutaneous collagenous vasculopathy
- Cutaneous mastocytoma
- Cutaneous polyarteritis nodosa
- Cutaneous sclerosis
- Cutis laxa, autosomal dominant
- Cutis laxa, autosomal recessive type 1
- Cutis marmorata telangiectatica congenita
- Cutis verticis gyrata
- Dahlberg Borer Newcomer syndrome
- Darier disease
- Deafness conductive ptosis skeletal anomalies
- Deafness enamel hypoplasia nail defects
- Deafness-lymphedema-leukemia syndrome
- Deficiency of interleukin-1 receptor antagonist
- Dermal eccrine cylindroma
- Dermatitis herpetiformis
- Dermatofibroma – Not a rare disease
- Dermatofibrosarcoma protuberans
- Dermatomyositis
- Dermatoosteolysis Kirghizian type
- Dermatopathia pigmentosa reticularis
- Dermatosparaxis Ehlers-Danlos syndrome
- Dermochondrocorneal dystrophy of François
- Dermoodontodysplasia
- Diffuse cutaneous systemic sclerosis
- Diffuse dermal angiomatosis
- Disseminated superficial actinic porokeratosis
- DOLK-CDG (CDG-Im)
- Dominant dystrophic epidermolysis bullosa
- DOOR syndrome
- Dowling-Degos disease
- Dubowitz syndrome
- Dykes Markes Harper syndrome
- Dyschromatosis symmetrica hereditaria 1
- Dyschromatosis universalis hereditaria
- Dyskeratosis congenita
- Dyskeratosis congenita autosomal dominant
- Dyskeratosis congenita autosomal recessive
- Dyskeratosis congenita X-linked
- Dystrophic epidermolysis bullosa
- Ectodermal dysplasia skin fragility syndrome
- Ectodermal dysplasia trichoodontoonychial type
- Ectodermal dysplasia with natal teeth Turnpenny type
- Ectodermal dysplasia, hidrotic, Christianson-Fourie type
- EEC syndrome
- EEM syndrome
- Ehlers-Danlos syndrome, dysfibronectinemic type
- Elastoderma
- Elastosis perforans serpiginosa
- Ellis-Van Creveld syndrome
- Encephalocraniocutaneous lipomatosis
- Eosinophilic pustular folliculitis
- Epidermodysplasia verruciformis
- Epidermolysa bullosa simplex with muscular dystrophy
- Epidermolysis bullosa
- Epidermolysis bullosa acquisita
- Epidermolysis bullosa simplex
- Epidermolysis bullosa simplex with mottled pigmentation
- Epidermolysis bullosa simplex, Dowling-Meara type
- Epidermolysis bullosa simplex, generalized
- Epidermolysis bullosa simplex, localized
- Epidermolysis bullosa simplex, Ogna type
- Epidermolysis bullosa, lethal acantholytic
- Epidermolytic ichthyosis
- Epidermolytic palmoplantar keratoderma
- Erdheim-Chester disease
- Erythema elevatum diutinum
- Erythema multiforme
- Erythema nodosum, idiopathic
- Erythrokeratoderma ”en cocardes”
- Erythrokeratodermia variabilis et progressiva
- Erythromelalgia
- Erythropoietic uroporphyria associated with myeloid malignancy
- Extranodal nasal NK/T cell lymphoma
- Fabry disease
- Facial ectodermal dysplasia
- Familial atypical multiple mole melanoma syndrome – Not a rare disease
- Familial cold autoinflammatory syndrome
- Familial cutaneous collagenoma
- Familial dermographism
- Familial Dupuytren contracture – Not a rare disease
- Familial dysautonomia
- Familial joint instability syndrome
- Familial multiple lipomatosis
- Familial multiple trichodiscomas
- Familial partial lipodystrophy associated with PLIN1 mutations – See Familial partial lipodystrophy
- Familial partial lipodystrophy associated with PPARG mutations
- Familial partial lipodystrophy due to AKT2 mutations – See Familial partial lipodystrophy
- Familial partial lipodystrophy type 2
- Familial partial lipodystrophy type Köbberling
- Familial reactive perforating collagenosis
- Familiar chronic mucocutaneous candidiasis – Not a rare disease
- Fanconi anemia
- Farber disease
- Febrile Ulceronecrotic Mucha-Habermann disease
- Fibrodysplasia ossificans progressiva
- Flynn Aird syndrome
- Focal dermal hypoplasia
- Focal facial dermal dysplasia
- Fox-Fordyce disease
- Frontal fibrosing alopecia
- Frontonasal dysplasia with alopecia and genital anomaly – See Frontonasal dysplasia
- GAPO syndrome
- Gardner syndrome
- Gardner-Diamond syndrome
- Gastrocutaneous syndrome
- Gaucher disease perinatal lethal
- Generalized junctional epidermolysis bullosa, non-Herlitz type – See Junctional epidermolysis bullosa
- Generalized pustular psoriasis
- Genuine diffuse phlebectasia
- Geroderma osteodysplastica
- Giant congenital nevus
- Gingival fibromatosis with hypertrichosis
- GM3 synthase deficiency
- Gorlin Chaudhry Moss syndrome
- Graham-Little-Piccardi-Lassueur syndrome
- Granuloma annulare
- Granulomatous rosacea
- Granulomatous slack skin disease
- Griscelli syndrome type 1
- Griscelli syndrome type 2
- Griscelli syndrome type 3
- Grover’s disease – Not a rare disease
- Guttate psoriasis
- Hailey-Hailey disease
- Haim-Munk syndrome
- Hair defect-photosensitivity-intellectual disability syndrome
- Hairy elbows
- Halal Setton Wang syndrome
- Hallermann-Streiff syndrome
- Halo nevus
- Hard skin syndrome Parana type
- Harlequin ichthyosis
- Hartnup disease
- Hennekam syndrome
- Hepatoerythropoietic porphyria
- Hereditary coproporphyria
- Hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis
- Hereditary hemorrhagic telangiectasia
- Hereditary hemorrhagic telangiectasia type 2
- Hereditary hemorrhagic telangiectasia type 3
- Hereditary hemorrhagic telangiectasia type 4
- Hereditary leiomyomatosis and renal cell cancer
- Hereditary lymphedema type II
- Hereditary mucoepithelial dysplasia
- Hereditary pancreatitis
- Hermansky Pudlak syndrome 2
- Hidradenitis suppurativa – Not a rare disease
- Histiocytosis-lymphadenopathy plus syndrome
- Holocarboxylase synthetase deficiency
- Hyaline fibromatosis syndrome
- Hydroa vacciniforme
- Hydroa vacciniforme, familial
- Hyper-IgD syndrome
- Hyperkeratosis lenticularis perstans
- Hypermobile Ehlers-Danlos syndrome
- Hypertrichosis lanuginosa, acquired
- Hypohidrotic ectodermal dysplasia
- Hypohidrotic ectodermal dysplasia autosomal recessive
- Hypohidrotic ectodermal dysplasia with hypothyroidism and ciliary dyskinesia
- Hypomelanosis of Ito
- Hypotrichosis simplex
- Hypotrichosis-lymphedema-telangiectasia syndrome
- Ichthyosis alopecia eclabion ectropion intellectual disability
- Ichthyosis bullosa of Siemens
- Ichthyosis cheek eyebrow syndrome
- Ichthyosis follicularis atrichia photophobia syndrome
- Ichthyosis hystrix, Curth Macklin type
- Ichthyosis lamellar 1
- Ichthyosis lamellar, autosomal dominant
- Ichthyosis prematurity syndrome
- Ichthyosis tapered fingers midline groove up
- Ichthyosis vulgaris
- Ichthyosis, acquired
- Ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis
- Ichthyosis-intellectual disability-dwarfism-renal impairment
- Incontinentia pigmenti
- Infantile myofibromatosis
- Inflammatory linear verrucous epidermal nevus
- Iridogoniodysgenesis type 1
- Isolated anterior cervical hypertrichosis
- Johanson-Blizzard syndrome
- Johnson neuroectodermal syndrome
- Junctional epidermolysis bullosa generalized intermediate – See Epidermolysis bullosa
- Junctional epidermolysis bullosa inversa – See Epidermolysis bullosa
- Junctional epidermolysis bullosa, Herlitz type – See Epidermolysis bullosa
- Juvenile dermatomyositis
- Juvenile polyposis syndrome
- Keratoderma palmoplantar deafness
- Keratoderma palmoplantar spastic paralysis
- Keratoderma palmoplantaris transgrediens
- Keratolytic winter erythema
- Keratosis follicularis dwarfism and cerebral atrophy
- Keratosis follicularis spinulosa decalvans
- Keratosis palmoplantaris striata 1
- Keratosis palmoplantaris striata 3
- KID syndrome
- Kindler syndrome
- Klippel-Trenaunay syndrome
- Knuckle pads, leuconychia and sensorineural deafness
- Kohlschutter Tonz syndrome
- Kyphoscoliotic Ehlers-Danlos syndrome
- Kyrle disease
- Lacrimo-auriculo-dento-digital syndrome
- Lamellar ichthyosis
- Laryngoonychocutaneous syndrome – See Epidermolysis bullosa
- Late-onset junctional epidermolysis bullosa – See Junctional epidermolysis bullosa
- Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
- Ledderhose disease
- Legius syndrome
- Lelis syndrome
- LEOPARD syndrome
- Leprechaunism
- Leukoencephalopathy palmoplantar keratoderma
- Leukonychia totalis
- Lichen planopilaris
- Lichen planus pemphigoides
- Lichen planus pigmentosus
- Lichen sclerosus
- Limb-mammary syndrome
- Limited cutaneous systemic sclerosis
- Limited systemic sclerosis
- Linear and whorled nevoid hypermelanosis
- Linear IgA disease
- Linear lichen planus
- Linear nevus sebaceous syndrome
- Linear scleroderma
- LIPE-related familial partial lipodystrophy – See Familial partial lipodystrophy
- Lipedema – Not a rare disease
- Lipodystrophy, familial partial, type 5 – See Familial partial lipodystrophy
- Lipoid proteinosis of Urbach and Wiethe
- Lissencephaly 2
- Localized junctional epidermolysis bullosa, non-Herlitz type – See Junctional epidermolysis bullosa
- Localized scleroderma
- Loose anagen hair syndrome
- Lupus erythematosus tumidus
- Lymphedema and cerebral arteriovenous anomaly
- Lymphedema-distichiasis syndrome
- Lymphocytic infiltrate of Jessner
- Lymphomatoid papulosis
- Macules hereditary congenital hypopigmented and hyperpigmented
- Maffucci syndrome
- Majeed syndrome
- Malignant Atrophic Papulosis
- Mandibuloacral dysplasia with type A lipodystrophy
- Mandibuloacral dysplasia with type B lipodystrophy
- Marie Unna congenital hypotrichosis
- Marshall syndrome
- McCune-Albright syndrome
- Megalencephaly-capillary malformation syndrome
- Meleda disease
- Melkersson-Rosenthal syndrome
- Menkes disease
- Merkel cell carcinoma
- Mevalonic aciduria
- Microcystic lymphatic malformation
- Microphthalmia with linear skin defects syndrome
- Milroy disease
- Monilethrix
- Morphea
- MPDU1-CDG (CDG-If)
- MPI-CDG (CDG-Ib)
- Muckle-Wells syndrome
- Mucopolysaccharidosis type III
- Mucous membrane pemphigoid
- Muir-Torre syndrome
- Multicentric reticulohistiocytosis
- Multiple café-au-lait spots
- Multiple fibrofolliculoma familial
- Multiple sulfatase deficiency
- Multiple symmetric lipomatosis
- Musculocontractural Ehlers-Danlos syndrome
- Naegeli syndrome
- Nail-patella syndrome
- Nakajo Nishimura syndrome
- Naxos disease
- Necrobiotic xanthogranuloma
- Nelson syndrome
- Neonatal Onset Multisystem Inflammatory disease
- Neonatal progeroid syndrome
- Nephrogenic Systemic Fibrosis
- Nestor-guillermo progeria syndrome
- Netherton syndrome
- Neu Laxova syndrome
- Neurocutaneous melanosis
- Neurofibromatosis-Noonan syndrome
- Nevoid basal cell carcinoma syndrome
- Nevus comedonicus syndrome
- Nevus of Ito
- Nodular nonsuppurative panniculitis
- Nonbullous congenital ichthyosiform erythroderma
- Noonan syndrome
- Noonan syndrome 1 – See Noonan syndrome
- Noonan syndrome 2 – See Noonan syndrome
- Noonan syndrome 3 – See Noonan syndrome
- Noonan syndrome 4 – See Noonan syndrome
- Noonan syndrome 5 – See Noonan syndrome
- Noonan syndrome 6 – See Noonan syndrome
- Noonan-like syndrome with loose anagen hair
- Occipital horn syndrome
- Oculocerebral syndrome with hypopigmentation
- Oculocutaneous albinism type 1
- Oculocutaneous albinism type 1B
- Oculocutaneous albinism type 2
- Oculocutaneous albinism type 3
- Oculodentodigital dysplasia
- Oculoectodermal syndrome
- Odonto onycho dysplasia with alopecia
- Odontomicronychial dysplasia
- Odontoonychodermal dysplasia
- Odontotrichomelic syndrome
- Oliver syndrome
- Olmsted syndrome
- Onychocytic matricoma
- Onychodystrophy-anonychia
- Orofaciodigital syndrome 1
- Pachydermoperiostosis
- Pachyonychia congenita
- Palmoplantar keratoderma
- Palmoplantar keratoderma-sclerodactyly syndrome
- Papillon Lefevre syndrome
- Parapsoriasis
- Parkes Weber syndrome
- Peeling skin syndrome
- PEHO syndrome
- Pemphigus vulgaris
- Periodontal Ehlers-Danlos syndrome
- Peutz-Jeghers syndrome
- Piebaldism
- Pigmented purpuric dermatosis
- Pili annulati
- Pili torti
- Pili torti developmental delay neurological abnormalities
- Pilodental dysplasia with refractive errors
- Pilomatrixoma
- Pinheiro Freire-Maia Miranda syndrome
- Pityriasis lichenoides
- Pityriasis lichenoides chronica
- Pityriasis lichenoides et varioliformis acuta
- Pityriasis rubra pilaris
- PMM2-CDG (CDG-Ia)
- Poikiloderma with neutropenia
- Popliteal pterygium syndrome, Bartsocas-Papas type
- Porokeratosis of Mibelli
- Porokeratosis, disseminated superficial actinic 1
- Porokeratosis, disseminated superficial actinic 2
- Porphyria cutanea tarda
- Pretibial epidermolysis bullosa
- Primary cutaneous amyloidosis
- Progeria
- Progeroid short stature with pigmented nevi
- Progeroid syndrome Petty type
- Progestogen hypersensitivity
- Progressive osseous heteroplasia
- Prolidase deficiency
- Proliferating trichilemmal cyst
- Proteus syndrome
- Proteus-like syndrome
- Pruritic urticarial papules plaques of pregnancy
- Pseudoainhum
- Pseudohypoparathyroidism type 1A
- Pseudohypoparathyroidism type 1C
- Pseudopelade of Brocq
- Pseudopseudohypoparathyroidism
- Pseudoxanthoma elasticum
- Punctate palmoplantar keratoderma type 2
- Punctate palmoplantar keratoderma type I
- Pustulosis palmaris et plantaris
- Pyoderma gangrenosum
- Pyogenic arthritis, pyoderma gangrenosum and acne
- Pyogenic granuloma – Not a rare disease
- Pyramidal molars-abnormal upper lip syndrome
- Quinquaud folliculitis decalvans
- Rabson-Mendenhall syndrome
- Recessive dystrophic epidermolysis bullosa-generalized other
- Red skin pigment anomaly of New Guinea
- Refsum disease
- Reynolds syndrome
- Rhabdomyomatous mesenchymal hamartoma
- Roch-Leri mesosomatous lipomatosis
- Rombo syndrome
- Rosai-Dorfman disease
- SAPHO syndrome
- Satoyoshi syndrome
- Scalp defects postaxial polydactyly
- Scalp ear nipple syndrome
- SCARF syndrome
- Schinzel Giedion syndrome
- Schwannomatosis
- Scleromyxedema
- Seborrheic keratosis – Not a rare disease
- Severe generalized recessive dystrophic epidermolysis bullosa
- Sezary syndrome
- SHORT syndrome
- Sjogren-Larsson syndrome
- Sjogren-Larsson-like syndrome
- Slow-channel congenital myasthenic syndrome
- Sneddon syndrome
- Spinocerebellar ataxia 34
- Spitz nevus
- Spondylodysplastic Ehlers-Danlos syndrome
- Spondyloepimetaphyseal dysplasia joint laxity
- SRD5A3-CDG (CDG-Iq)
- Steatocystoma multiplex
- Steatocystoma multiplex with natal teeth
- Stevens-Johnson syndrome/toxic epidermal necrolysis
- Stiff skin syndrome
- Stoll Alembik Finck syndrome
- Sturge-Weber syndrome
- Subcorneal pustular dermatosis
- Swyer syndrome
- Syringocystadenoma papilliferum
- Systemic scleroderma
- TARP syndrome
- Taurodontia, absent teeth, sparse hair syndrome
- Telfer Sugar Jaeger syndrome
- Temple-Baraitser syndrome
- Tietz syndrome
- Transient bullous dermolysis of the newborn
- Tricho-dento-osseous syndrome
- Trichodental syndrome
- Trichomegaly with intellectual disability, dwarfism and pigmentary degeneration of retina
- Trichorhinophalangeal syndrome type 1
- Trichorhinophalangeal syndrome type 2
- Trichorhinophalangeal syndrome type 3
- Trichostasis spinulosa
- Trichothiodystrophy
- Tuberous sclerosis complex
- Tumor necrosis factor receptor-associated periodic syndrome
- Twenty-nail dystrophy
- Tylosis with esophageal cancer
- Tyrosinemia type 2
- Ulerythema ophryogenesis
- Uncombable hair syndrome
- UV sensitive syndrome
- Van Den Bosch syndrome
- Variegate porphyria
- Vascular Ehlers-Danlos syndrome
- Verrucous nevus acanthokeratolytic
- Vici syndrome
- Vitiligo – Not a rare disease
- Vohwinkel syndrome
- Waardenburg syndrome type 1
- Waardenburg syndrome type 2
- Waardenburg syndrome type 3
- Waardenburg syndrome type 4
- Wells syndrome
- Werner syndrome
- Weyers acrofacial dysostosis
- White sponge nevus of cannon
- Wiskott Aldrich syndrome
- Witkop syndrome
- Woolly hair hypotrichosis everted lower lip and outstanding ears
- Woolly hair syndrome
- Wrinkly skin syndrome
- Wyburn-Mason syndrome
- X-linked congenital generalized hypertrichosis
- X-linked dominant chondrodysplasia punctata 2
- X-linked hypohidrotic ectodermal dysplasia
- X-linked ichthyosis
- X-linked intellectual disability – short stature – obesity
- Xanthoma disseminatum
- Xeroderma pigmentosum
- Xeroderma pigmentosum, variant type
- Yellow nail syndrome
- Yemenite deaf-blind hypopigmentation syndrome
- Zlotogora syndrome
Source Link -: https://rarediseases.info.nih.gov/diseases/diseases-by-category/22/skin-diseases