SE-ATLAS

Keratoderma hereditarium mutilans mit Ichthyose Dermatofibrosarcoma protuberans Erythrodermie, ichthyosiforme kongenitale Selbstheilendes Kollodium-Baby Primär kutanes B-Zell-Lymphom, aggressives Hautkrankheit, autoimmune bullöse Primär kutanes T-Zell-Lymphom, aggressives Primär kutanes B-Zell-Lymphom, indolentes Alopecia totalis Alopecia universalis Dermatitis herpetiformis Syndrom des linearen verrukösen Naevus Piebaldismus Naevus, panfollikulärer, kongenitaler Syndrom des linearen Naevus sebaceus Piebaldismus - neurologische Anomalien Pemphigoid, bullöses Syringocystadenoma papilliferum Didymosis aplasticosebacea Pemphigus vulgaris Ostiumnaevus, ekkriner porokeratotischer Peeling-Skin-Syndrom, lokalisiertes Ichthyose, exfoliative PTEN-Hamartom-Tumor-Syndrom Ichthyose-Hypotrichose-Syndrom Pili torti Sézary-Syndrom Albinismus, okulokutaner, Typ 1, temperaturempfindlicher Melanozytose, neurokutane Hypomelanose Typ Ito NEVADA-Syndrom Pili torti - Entwicklungsverzögerung - neurologische Anomalien Monilethrix SCALP-Syndrom Mycosis fungoides-Varianten Albinismus, okulokutaner, Typ 1 Selbstheilendes Kollodiumbaby, akrales Albinismus, okulokutaner , Typ 1, minimal-pigmentierter Primär kutanes B-Zell-Lymphom Waardenburg-Syndrom Okulokutaner Albinismus, syndromaler Chédiak-Higashi-Syndrom Lose Anagenhaar-Syndrom Annular epidermolytic ichthyosis Ringed hair disease Pilomatrixoma Woolly hair nevus Woolly hair Paraneoplastic pemphigus Oculocutaneous albinism type 7 Cutaneous neuroendocrine carcinoma Marie Unna hereditary hypotrichosis Osteosclerosis-ichthyosis-premature ovarian failure syndrome Cervical hypertrichosis-peripheral neuropathy syndrome Dermatopathia pigmentosa reticularis Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Familial progressive hyperpigmentation Hypertrichosis cubiti Pili bifurcati Acquired hypertrichosis lanuginosa Onychocytic matricoma Dowling-Degos disease Acromelanosis Autosomal dominant epidermolytic ichthyosis Generalized peeling skin syndrome Hypertrichosis lanuginosa congenita Lamellar ichthyosis Rare nail tumor Dyschromatosis symmetrica hereditaria Muir-Torre syndrome Linear and whorled nevoid hypermelanosis Peeling skin syndrome type A Albinism-deafness syndrome Hair defect-photosensitivity-intellectual disability syndrome Non-Langerhans cell histiocytosis Erythrokeratodermia variabilis Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome Trichofolliculoma Superficial epidermolytic ichthyosis Diffuse lymphatic malformation Uncombable hair syndrome Peeling skin syndrome type B Multicentric reticulohistiocytosis Reticulate acropigmentation of Kitamura Onychomatricoma Bathing suit ichthyosis Harlequin ichthyosis Hermansky-Pudlak syndrome due to BLOC-3 deficiency Familial multiple trichoepithelioma CLOVES syndrome Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome Peeling skin syndrome type C Oculocutaneous albinism type 1A Primary cutaneous T-cell lymphoma Alopecia antibody deficiency Hermansky-Pudlak syndrome Osteopathia striata-pigmentary dermopathy-white forelock syndrome Autoinflammatory syndrome with skin involvement PASH syndrome Recessive X-linked ichthyosis Generalized eruptive histiocytosis Hermansky-Pudlak syndrome due to BLOC-2 deficiency Oculocutaneous albinism type 3 Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Oculocutaneous albinism type 2 Benign cephalic histiocytosis Systemic disease with skin involvement Oculocutaneous albinism Nevus of Ota Generalized basaloid follicular hamartoma syndrome Familial normophosphatemic tumoral calcinosis Oculocutaneous albinism type 1B Oculocutaneous albinism type 4 Juvenile xanthogranuloma Nevus of Ito Oculocutaneous albinism type 5 Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Drug-induced lupus erythematosus Congenital smooth muscle hamartoma Proteus syndrome Xanthoma disseminatum Cowden syndrome Familial multiple fibrofolliculoma Crandall syndrome Familial progressive hyper- and hypopigmentation KID syndrome Congenital generalized hypertrichosis, Ambras type Papular xanthoma Infantile onset panniculitis with uveitis and systemic granulomatosis Naegeli-Franceschetti-Jadassohn syndrome Necrobiotic xanthogranuloma Frontonasal dysplasia-alopecia-genital anomalies syndrome Oculocutaneous albinism type 6 Familial melanoma CEDNIK syndrome Epidermal nevus syndrome Quinquaud folliculitis decalvans Familial cylindromatosis Generalized pustular psoriasis Atrichia with papular lesions Hermansky-Pudlak syndrome due to BLOC-1 deficiency Waardenburg syndrome type 1 Hypotrichosis simplex of the scalp Waardenburg syndrome type 2 Deaf blind hypopigmentation syndrome, Yemenite type Waardenburg syndrome type 3 Trichodental syndrome Follicular atrophoderma-basal cell carcinoma Hermansky-Pudlak syndrome type 8 Tricho-dento-osseous syndrome Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome Progressive nodular histiocytosis Oley syndrome Indeterminate cell histiocytosis Large congenital melanocytic nevus Proliferating trichilemmal cyst Hemihyperplasia-multiple lipomatosis syndrome Congenital reticular ichthyosiform erythroderma Familial keratoacanthoma Salt-and-pepper syndrome Ichthyosis-cheek-eyebrow syndrome Trichothiodystrophy Hereditary progressive mucinous histiocytosis Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Verrucous nevus Acanthokeratolytic verrucous nevus Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome Inflammatory linear verrucous epidermal nevus Trichodysplasia-xeroderma syndrome Netherton syndrome Congenital ichthyosis-microcephalus-tetraplegia syndrome Erdheim-Chester disease Ichthyosis-oral and digital anomalies syndrome Ichthyosis follicularis-alopecia-photophobia syndrome Hypotrichosis-deafness syndrome Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome Griscelli syndrome type 1 Graham Little-Piccardi-Lassueur syndrome Rare lymphatic malformation Griscelli syndrome type 3 Reynolds syndrome Hermansky-Pudlak syndrome due to AP-3 deficiency Griscelli syndrome type 2 Pemphigus erythematosus Pemphigus vegetans Hermansky-Pudlak syndrome type 9 Ichthyosis-prematurity syndrome Pemphigus foliaceus PENS syndrome Nevus comedonicus syndrome Granulomatous slack skin Phakomatosis spilorosea Gorlin syndrome Proteus-like syndrome Phakomatosis cesioflammea Dyschromatosis universalis hereditaria Phakomatosis cesiomarmorata Becker nevus syndrome Cystic hygroma Griscelli syndrome Hyperkeratosis-hyperpigmentation syndrome Macrocystic lymphatic malformation Bannayan-Riley-Ruvalcaba syndrome Rombo syndrome Noonan syndrome-like disorder with loose anagen hair Ichthyosis Microcystic lymphatic malformation Tietz syndrome Brooke-Spiegler syndrome Superficial pemphigus Bazex-Dupré-Christol syndrome PAPA syndrome Pili gemini Terminal osseous dysplasia-pigmentary defects syndrome Isolated anterior cervical hypertrichosis Familial tumoral calcinosis Mucous membrane pemphigoid Hereditary leiomyomatosis and renal cell cancer X-linked congenital generalized hypertrichosis Linear IgA dermatosis Epidermolysis bullosa acquisita Lichen planopilaris Gingival fibromatosis-hypertrichosis syndrome Ledderhose disease Hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome Hair anomaly Herpetiform pemphigus Scleroderma Syndromic recessive X-linked ichthyosis Rare disorder with hypertrichosis X-linked dominant chondrodysplasia punctata Alopecia Alopecia-intellectual disability syndrome Birt-Hogg-Dubé syndrome Frontal fibrosing alopecia Syndromic hair shaft abnormality Björnstad syndrome Tuberous sclerosis complex Ichthyosis hystrix gravior Inherited ichthyosis syndromic form Autosomal ichthyosis syndrome with prominent hair abnormalities Isolated hair shaft abnormality Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma Diffuse cutaneous systemic sclerosis Ichthyosis hystrix of Curth-Macklin Pemphigoid gestationis Calcifying aponeurotic fibroma Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma Superficial fibromatosis Autosomal recessive congenital ichthyosis Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome Oculocerebral hypopigmentation syndrome, Cross type H syndrome CLAPO syndrome Pseudopelade of Brocq Adult T-cell leukemia/lymphoma Pigmentation anomaly of the skin Limited cutaneous systemic sclerosis Hypopigmentation of the skin Primary cutaneous CD30+ T-cell lymphoproliferative disease Primary cutaneous lymphoma Familial generalized lentiginosis Hyperpigmentation of the skin Localized scleroderma Primary cutaneous marginal zone B-cell lymphoma Sjögren-Larsson syndrome Autosomal ichthyosis syndrome with fatal disease course Hereditary hypotrichosis with recurrent skin vesicles Infantile digital fibromatosis Extranodal nasal NK/T cell lymphoma Peeling skin syndrome Systemic sclerosis Infantile myofibromatosis Primary cutaneous gamma/delta-positive T-cell lymphoma Limited systemic sclerosis CREST syndrome MEDNIK-Syndrom Ichthyose-Syndrom, autosmales, mit weiteren assoziierten Symptomen Lymphom, primär kutanes, follikuläres T-Zell-Lymphom, subkutanes Pannikulitis-ähnliches Seltener Naevus Dyskeratosis congenita CHILD-Syndrom Ichthyose-Syndrom, autosmales, mit prominenten neurologischen Symptomen Barber-Say-Syndrom Ichthyose, keratinopathische Primär kutanes peripheres T-Zell-Lymphom, andernorts nicht klassifiziert B-Zell-Lymphom, diffuses großzelliges, primär kutanes, vom leg Typ Angorahaar-Naevus Hauttumor oder Hamartom, seltene Formen Hypotrichosis simplex Multiple selbstheilende squamöse Epitheliome Schleimhaut-Naevus, weißer Phakomatosis pigmento-keratotica Primär kutanes T-Zell-Lymphom, indolentes Phakomatosis pigmentovascularis ANE-Syndrom Katarakt-Hypertrichose-Intelligenzminderung-Syndrom Syndrom des akromegaloiden Gesichtes mit Hypertrichose Malignes Melanom der Mukosa Katarakt, kongenitale - Ichthyose Gardner-Syndrom