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 Ichthyose, anuläre epidermolytische Ringelhaare Pilomatrixom Wollhaarnaevus Wollhaare Pemphigus, paraneoplastischer Albinismus, okulokutaner, Typ 7 Karzinom, kutanes neuroendokrines Hypotrichose, hereditäre kongenitale, Typ Marie Unna Osteosklerose - Ichthyose - vorzeitige Ovarialinsuffizienz Hypertrichose der Hals-Vorderseite - periphere Neuropathie Dermatopathia pigmentosa reticularis Kongenitale Ichthyose-Intelligenzminderung-spastische Tetraplegie-Syndrom Hyperpigmentierung, familiäre progressive Hypertrichosis cubiti Pili bifurcati Hypertrichosis lanuginosa, erworbene Onychozytisches Matrikom Dowling-Degos-Krankheit Akromelanose Ichthyose, epidermolytische, autosomal-dominante Peeling-Skin-Syndrom, generalisiertes Hypertrichosis lanuginosa, kongenitale Ichthyose, lamelläre Nageltumor, seltener Dyschromatosis symmetrica hereditaria Muir-Torre-Syndrom Hypermelanose, nävoide, streifen- und wirbelförmige Peeling-Skin-Syndrom Typ A Albinismus - Schwerhörigkeit Haaranomalien - Photosensibilität - Intelligenzminderung Non-Langerhans-Zell-Histiozytose Erythrokeratodermia variabilis Wollhaare-Hypotrichose-evertierte Unterlippe-abstehende Ohren-Syndrom Trichofollikulom Ichthyose, epidermolytische superfizielle Lymphatische Fehlbildung, diffuse Syndrom der nicht kämmbaren Haare Peeling-Skin-Syndrom Typ B Retikulohistiozytose, multizentrische Retikuläre Hyperpigmentierung vom Typ Kitamura Onychomatrikom Bathing-suit-Ichthyose Harlekin-Ichthyose Hermansky-Pudlak-Syndrom durch BLOC-3-Defizienz Trichoepitheliom, familiäres multiples CLOVE-Syndrom Familiäre hyperphosphatämische tumorale Kalzinose/Hyperphosphatämische Hyperostose-Syndrom Peeling-Skin-Syndrom, generalisiertes, Typ C Albinismus, okulokutaner, Typ 1A Primär kutanes T-Zell-Lymphom Alopezie mit Antikörper-Mangel 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 syndrome Autosomal ichthyosis syndrome with other associated signs Primary cutaneous follicle center lymphoma Subcutaneous panniculitis-like T-cell lymphoma Rare nevus Dyskeratosis congenita CHILD syndrome Autosomal ichthyosis syndrome with prominent neurologic signs Barber-Say syndrome Keratinopathic ichthyosis Primary cutaneous peripheral T-cell lymphoma not otherwise specified Primary cutaneous diffuse large B-cell lymphoma, leg type Angora hair nevus Rare skin tumor or hamartoma Hypotrichosis simplex Multiple self-healing squamous epithelioma White sponge nevus Phakomatosis pigmentokeratotica Indolent primary cutaneous T-cell lymphoma Phakomatosis pigmentovascularis ANE syndrome Cataract-hypertrichosis-intellectual disability syndrome Hypertrichosis-acromegaloid facial appearance syndrome Malignant melanoma of the mucosa Congenital cataract-ichthyosis syndrome Gardner syndrome