|
Absence of fingerprints - congenital milia
|
(Orphanet:1658)
|
|
Acquired epidermolysis bullosa
|
(Orphanet:46487)
|
|
Acquired ichthyosis
|
(Orphanet:454)
|
|
Acral dystrophic epidermolysis bullosa
|
(Orphanet:158673)
|
|
Acrokeratoelastoidosis of Costa
|
(Orphanet:38)
|
|
Aggressive systemic mastocytosis
|
(Orphanet:98850)
|
|
Alopecia
|
(Orphanet:79364)
|
|
Autosomal dominant hyper-IgE syndrome
|
(Orphanet:2314)
|
|
Behçet disease
|
(Orphanet:117)
|
|
Benign cephalic histiocytosis
|
(Orphanet:157997)
|
|
Birt-Hogg-Dube syndrome
|
(Orphanet:122)
|
|
Blau syndrome
|
(Orphanet:90340)
|
|
Bullous lichen planus
|
(Orphanet:33408)
|
|
CINCA syndrome
|
(Orphanet:1451)
|
|
Centripetalis recessive dystrophic epidermolysis bullosa
|
(Orphanet:89841)
|
|
Chronic mucocutaneous candidiasis
|
(Orphanet:1334)
|
|
Classical mycosis fungoides
|
(Orphanet:2584)
|
|
Cowden syndrome
|
(Orphanet:201)
|
|
Cutaneous leukocytoclastic angiitis
|
(Orphanet:889)
|
|
Cutaneous lupus erythematosus
|
(Orphanet:535)
|
|
Cutaneous mastocytosis
|
(Orphanet:66646)
|
|
Darier disease
|
(Orphanet:218)
|
|
Dermatitis herpetiformis
|
(Orphanet:1656)
|
|
Dermatomyositis
|
(Orphanet:221)
|
|
Disseminated superficial actinic porokeratosis
|
(Orphanet:79152)
|
|
Drug rash with eosinophilia and systemic symptoms
|
(Orphanet:139402)
|
|
Dystrophic epidermolysis bullosa
|
(Orphanet:303)
|
|
Dystrophic epidermolysis bullosa pruriginosa
|
(Orphanet:89843)
|
|
Ehlers-Danlos syndrome, classic type
|
(Orphanet:287)
|
|
Eosinophilic granulomatosis with polyangiitis
|
(Orphanet:183)
|
|
Epidermodysplasia verruciformis
|
(Orphanet:302)
|
|
Epidermolysis bullosa simplex superficialis
|
(Orphanet:89839)
|
|
Epidermolysis bullosa simplex with mottled pigmentation
|
(Orphanet:79397)
|
|
Epidermolysis bullosa simplex with muscular dystrophy
|
(Orphanet:257)
|
|
Epidermolysis bullosa simplex, Ogna type
|
(Orphanet:79401)
|
|
Erythema elevatum diutinum
|
(Orphanet:90000)
|
|
Erythrokeratodermia - ataxia
|
(Orphanet:1955)
|
|
Erythrokeratodermia variabilis
|
(Orphanet:317)
|
|
Fabry disease
|
(Orphanet:324)
|
|
Familial cold urticaria
|
(Orphanet:47045)
|
|
Familial cutaneous collagenoma
|
(Orphanet:53296)
|
|
Familial keratoacanthoma
|
(Orphanet:493)
|
|
Familial multiple fibrofolliculoma
|
(Orphanet:338)
|
|
Familial multiple nevi flammei
|
(Orphanet:624)
|
|
Familial multiple trichoepithelioma
|
(Orphanet:867)
|
|
Fountain syndrome
|
(Orphanet:3219)
|
|
Generalized dominant dystrophic epidermolysis bullosa
|
(Orphanet:231568)
|
|
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
|
(Orphanet:79399)
|
|
Generalized eruptive histiocytosis
|
(Orphanet:157991)
|
|
Gorlin syndrome
|
(Orphanet:377)
|
|
Graham Little-Piccardi-Lassueur syndrome
|
(Orphanet:505)
|
|
Granulomatosis with polyangiitis
|
(Orphanet:900)
|
|
Hand-Schüller-Christian disease
|
(Orphanet:99873)
|
|
Hashimoto-Pritzker syndrome
|
(Orphanet:99872)
|
|
Hennekam-Beemer syndrome
|
(Orphanet:2135)
|
|
Hereditary acrokeratotic poikiloderma, Weary type
|
(Orphanet:2907)
|
|
Hereditary progressive mucinous histiocytosis
|
(Orphanet:158025)
|
|
Hyperimmunoglobulinemia D with periodic fever
|
(Orphanet:343)
|
|
Hyperkeratosis lenticularis perstans
|
(Orphanet:409)
|
|
Hyperkeratosis-hyperpigmentation syndrome
|
(Orphanet:1336)
|
|
Hypotrichosis - lymphedema - telangiectasia
|
(Orphanet:69735)
|
|
Hypotrichosis simplex
|
(Orphanet:55654)
|
|
Ichthyosis follicularis - alopecia - photophobia
|
(Orphanet:2273)
|
|
Ichthyosis hystrix of Curth-Macklin
|
(Orphanet:79503)
|
|
Inherited epidermolysis bullosa
|
(Orphanet:79361)
|
|
Jessner's lymphocytic infiltration of the skin
|
(Orphanet:33314)
|
|
Junctional epidermolysis bullosa
|
(Orphanet:305)
|
|
Juvenile dermatomyositis
|
(Orphanet:93672)
|
|
Juvenile hyaline fibromatosis
|
(Orphanet:2028)
|
|
Juvenile xanthogranuloma
|
(Orphanet:158000)
|
|
Keratoderma hereditarium mutilans
|
(Orphanet:494)
|
|
Keratosis follicularis spinulosa decalvans
|
(Orphanet:2340)
|
|
Keratosis pilaris atrophicans
|
(Orphanet:498)
|
|
Kerion celsi
|
(Orphanet:499)
|
|
Kindler syndrome
|
(Orphanet:2908)
|
|
Lichen amyloidosis
|
(Orphanet:49804)
|
|
Lichen planopilaris
|
(Orphanet:525)
|
|
Lipoid proteinosis
|
(Orphanet:530)
|
|
Lyme disease
|
(Orphanet:91546)
|
|
Maculopapular cutaneous mastocytosis
|
(Orphanet:79457)
|
|
Majeed syndrome
|
(Orphanet:77297)
|
|
Malakoplakia
|
(Orphanet:556)
|
|
Malignant atrophic papulosis
|
(Orphanet:679)
|
|
Monilethrix
|
(Orphanet:573)
|
|
Multicentric reticulohistiocytosis
|
(Orphanet:139436)
|
|
Neurofibromatosis type 2
|
(Orphanet:637)
|
|
Non-epidermolytic palmoplantar keratoderma
|
(Orphanet:2337)
|
|
Oley syndrome
|
(Orphanet:79458)
|
|
Oral erosive lichen
|
(Orphanet:31142)
|
|
Orofaciodigital syndrome type 1
|
(Orphanet:2750)
|
|
PTEN hamartoma tumor syndrome
|
(Orphanet:306498)
|
|
Pachydermoperiostosis
|
(Orphanet:2796)
|
|
Papular xanthoma
|
(Orphanet:158008)
|
|
Phakomatosis pigmentovascularis
|
(Orphanet:2875)
|
|
Pityriasis rubra pilaris
|
(Orphanet:2897)
|
|
Polyarteritis nodosa
|
(Orphanet:767)
|
|
Porokeratosis
|
(Orphanet:79358)
|
|
Porokeratosis of Mibelli
|
(Orphanet:735)
|
|
Pretibial dystrophic epidermolysis bullosa
|
(Orphanet:79410)
|
|
Primary cutaneous anaplastic large cell lymphoma
|
(Orphanet:300865)
|
|
Primary cutaneous lymphoma
|
(Orphanet:542)
|
|
Progressive nodular histiocytosis
|
(Orphanet:158022)
|
|
Progressive osseous heteroplasia
|
(Orphanet:2762)
|
|
Prolidase deficiency
|
(Orphanet:742)
|
|
Proteus syndrome
|
(Orphanet:744)
|
|
Pseudo-pelade of Brocq
|
(Orphanet:129)
|
|
Pseudoxanthoma elasticum
|
(Orphanet:758)
|
|
Quinquaud's folliculitis decalvans
|
(Orphanet:346)
|
|
Recessive dystrophic epidermolysis bullosa inversa
|
(Orphanet:79409)
|
|
Recessive dystrophic epidermolysis bullosa-generalized other
|
(Orphanet:89842)
|
|
Rombo syndrome
|
(Orphanet:3110)
|
|
Schnitzler syndrome
|
(Orphanet:37748)
|
|
Scleroderma
|
(Orphanet:801)
|
|
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
|
(Orphanet:137608)
|
|
Severe generalized recessive dystrophic epidermolysis bullosa
|
(Orphanet:79408)
|
|
Stuccokeratosis
|
(Orphanet:830)
|
|
Sweet syndrome
|
(Orphanet:3243)
|
|
Syringocystadenoma papilliferum
|
(Orphanet:840)
|
|
TRAPS syndrome
|
(Orphanet:32960)
|
|
Tuberous sclerosis
|
(Orphanet:805)
|
|
Ulerythema ophryogenesis
|
(Orphanet:3406)
|
|
Wells syndrome
|
(Orphanet:901)
|
|
Xanthoma disseminatum
|
(Orphanet:158003)
|