SE-ATLAS

ADULT syndrome ANE syndrome AREDYLD syndrome Absence of fingerprints-congenital milia syndrome Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome Acquired ichthyosis Acral peeling skin syndrome Acral self-healing collodion baby Acrodermatitis continua suppurativa Hallopeau Acrofacial dysostosis, Weyers type Acrogeria Acrokeratoelastoidosis of Costa Acrokeratosis verruciformis of Hopf Acroosteolysis-keloid-like lesions-premature aging syndrome Acute intermittent porphyria Aderhautatrophie-Alopezie-Syndrom Adulte T-Zell-Leukämie/Lymphom Aggressive primary cutaneous B-cell lymphoma Aggressive primary cutaneous T-cell lymphoma Akrokeratodermie, genetisch bedingte Albinism-deafness syndrome Albinismus, okulokutaner, Typ 6 Aleukemic mast cell leukemia Alopecia antibody deficiency Alopecia totalis Alopecia universalis Alopecia-contractures-dwarfism-intellectual disability syndrome Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Alopezie Alopezie-Intelligenzminderung-Syndrom Amelo-onycho-hypohidrotisches Syndrom Amelocerebrohypohidrotic syndrome Anetodermie, familiäre Angioosteohypertrophic syndrome Angora hair nevus Anhidrotische ektodermale Dysplasie-Immundefekt-Osteopetrose-Lymphödem-Syndrom Ankyloblepharon-ektodermale Defekte-Lippen-Kiefer-Gaumenspalte-Syndrom Annular epidermolytic ichthyosis Anonychia congenita totalis Anonychie mit umschriebener Pigmentierung Anonychie-Onychodystrophie-Syndrom Aplasia cutis congenita Aplasia cutis congenita-intestinal lymphangiectasia syndrome Aplasia cutis-myopia syndrome Arterial-Tortuosity-Syndrom Ataxia-Teleangiectasia Atrichie mit papulösen Läsionen Atrophodermia vermiculata Autoimmune bullous skin disease Autosomal dominant cutis laxa Autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature Autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature Autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature Autosomal dominant epidermolytic ichthyosis Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering Autosomal dominant generalized epidermolysis bullosa simplex, intermediate form Autosomal dominant generalized epidermolysis bullosa simplex, severe form Autosomal dominant hypohidrotic ectodermal dysplasia Autosomal dominant isolated diffuse palmoplantar keratoderma Autosomal dominant multiple pterygium syndrome Autosomal dominant palmoplantar keratoderma and congenital alopecia Autosomal erythropoietic protoporphyria Autosomal ichthyosis syndrome with fatal disease course Autosomal ichthyosis syndrome with other associated signs Autosomal ichthyosis syndrome with prominent neurologic signs Autosomal recessive cutis laxa type 1 Autosomal recessive cutis laxa type 2 Autosomal recessive disease with focal palmoplantar keratoderma as a major feature Autosomal recessive generalized dystrophic epidermolysis bullosa, severe form Autosomal recessive isolated diffuse palmoplantar keratoderma Autosomal recessive palmoplantar keratoderma and congenital alopecia Autosomal-dominante Tricho-Odonto-Onycho-Dysplasie - Syndaktylie Autosomal-rezessive Krankheit mit assoziierter punktierter Palmoplantarkeratose als Hauptmerkmal Autosomal-rezessive Krankheit mit diffuser Palmoplantarkeratose als Hauptmerkmal B4GALT7-assoziiertes spondylodysplastisches Ehlers-Danlos-Syndrom Bannayan-Riley-Ruvalcaba-Syndrom Barber-Say syndrome Bartsocas-Papas syndrome Basal epidermolysis bullosa simplex Bathing suit ichthyosis Bazex-Dupré-Christol-Syndrom Becker Naevus-Syndrom Birt-Hogg-Dubé-Syndrom Björnstad-Syndrom Blepharo-cheilo-dentales Syndrom Bloom-Syndrom Blue rubber bleb-Naevus Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency Brain-lung-thyroid syndrome Brittle cornea syndrome Brooke-Spiegler-Syndrom Bullous pemphigoid Buschke-Ollendorff-Syndrom Böök syndrome CEDNIK-Syndrom CHILD syndrome CHIME syndrome CLAPO-Syndrom CLOVES syndrome COFS-Syndrom CREST syndrome Carney-Komplex Cartilage-hair hypoplasia Carvajal-Syndrom Cataract-hypertrichosis-intellectual disability syndrome Cervical hypertrichosis-peripheral neuropathy syndrome Chilblain-Lupus Chondrodysplasia punctata, X-chromosomal-dominante Chondroectodermal dysplasia with night blindness Chronic cutaneous lupus erythematosus Chédiak-Higashi syndrome Classic mast cell leukemia Classical Ehlers-Danlos syndrome Cockayne syndrome Cockayne syndrome type 1 Cockayne syndrome type 2 Cockayne syndrome type 3 Congenital erythropoietic porphyria Congenital ichthyosiform erythroderma Congenital lethal erythroderma Congenital panfollicular nevus Congenital smooth muscle hamartoma Cooks-Syndrom Corneodermatoosseous syndrome Cowden syndrome Crandall-Syndrom Cranioectodermal dysplasia Cronkhite-Canada-Syndrom Cutaneous neuroendocrine carcinoma Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome Cutis laxa Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies Cutis laxa, autosomal-rezessive, Typ 2A Cutis laxa, autosomal-rezessive, Typ 2B Cutis marmorata telangiectatica congenita Cutis verticis gyrata, primäre DOORS-Syndrom Dahlberg-Borer-Newcomer syndrome Darier-Krankheit De Barsy-Syndrom DeBarsy-Syndrom, ALDH18A1-abhängiges Dermatitis herpetiformis Dermatofibrosarcoma protuberans Dermatomyositis Dermatoosteolysis, Kirghizian type Dermatopathia pigmentosa reticularis Dermochondrocorneal dystrophy Dermoodontodysplasia Dermotrichales Syndrom Didymosis aplasticosebacea Diffuse Palmoplantarkeratose mit schmerzhaften Fissuren Diffuse lymphatic malformation Diffuse palmoplantar keratoderma, Bothnian type Diffuse palmoplantar keratoderma-acrocyanosis syndrome Disease with diffuse palmoplantar keratoderma as a major feature Disease with focal palmoplantar keratoderma as a major feature Disease with punctate palmoplantar keratoderma as a major feature Disseminated superficial actinic porokeratosis Dowling-Degos disease Dubowitz-Syndrom Dyschromatosis symmetrica hereditaria Dyschromatosis universalis hereditaria Dyskeratosis congenita Dysplasie, ektodermale - natale Zähne, Typ Turnpenny Dysplasie, ektodermale hypohidrotische, autosomal-rezessive Dysplasie, ektodermale, reiner Haar-Nagel-Typ Dysplasie, odonto-onycho-dermale Dysplasie, okulo-dento-digitale Dystrophic epidermolysis bullosa Dystrophie, bullöse, hereditäre, makulärer Typ EEC syndrome and related disorders EEC-Syndrom EEM-Syndrom Ectodermal dysplasia, trichoodontoonychial type Ectodermal dysplasia-blindness syndrome Ectodermal dysplasia-hyperhidrosis-cutaneous syndactyly syndrome Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome Ectodermal dysplasia-pili torti-cutaneous syndactyly syndrome Ectodermal dysplasia-skin fragility syndrome Ehlers-Danlos syndrome Ehlers-Danlos syndrome type 1 Ehlers-Danlos syndrome type 2 Ehlers-Danlos syndrome type 7A Ehlers-Danlos syndrome type 7B Ehlers-Danlos syndrome with periventricular heterotopia Ehlers-Danlos-Syndrom Typ 10 Ehlers-Danlos-Syndrom, Arthrochalasie-Typ Ehlers-Danlos-Syndrom, Dermatosparaxis Typ Ehlers-Danlos-Syndrom, X-chromosomales Ehlers-Danlos-Syndrom, kardio-valvulärer Typ Ehlers-Danlos-Syndrom, klassisch-ähnlicher Typ 1 Ehlers-Danlos-Syndrom, muskulo-kontrakturaler Typ Ehlers-Danlos-Syndrom, parodontaler Typ Ehlers-Danlos/Osteogenesis imperfecta-Syndrom Ektodermale Dysplasie Ektodermale Dysplasie-sensorineurale Schwerhörigkeit-Syndrom Ellis Van Creveld syndrome Epidermale Krankheit, genetisch bedingte Epidermalnaevus, inflammatorischer lineärer verruköser Epidermolysis bullosa simplex Epidermolysis bullosa simplex due to BP230 deficiency Epidermolysis bullosa simplex due to exophilin 5 deficiency Epidermolysis bullosa simplex mit Muskeldystrophie Epidermolysis bullosa simplex superficialis Epidermolysis bullosa simplex with anodontia/hypodontia Epidermolysis bullosa simplex with circinate migratory erythema Epidermolysis bullosa simplex with mottled pigmentation Epidermolysis bullosa simplex with pyloric atresia Epidermolysis bullosa simplex, autosomal-rezessive, K14 Epidermolysis bullosa, akantholytische letale Epidermolysis bullosa, dystrophe pruriginöse Epidermolysis bullosa, dystrophe zentripetale Epidermolysis bullosa, dystrophe, generalisierte, autosomal-dominante Epidermolysis bullosa, dystrophe, generalisierte, autosomal-rezessive, intermediäre Form Epidermolysis bullosa, erworbene Epidermolysis bullosa, hereditäre Epidermolysis bullosa, junktionale, non-Herlitz Typ Epidermolytic palmoplantar keratoderma Erythema palmare hereditarium Erythrodermie, ichthyosiforme retikuläre, kongenitale Form Erythrokeratoderma ''en cocardes Erythrokeratoderma variabilis progressiva Erythrokeratodermia variabilis Erythrokeratodermie, genetisch bedingte Erythromelalgia Exfoliative ichthyosis Extranodal nasal NK/T cell lymphoma FLOTCH syndrome Familial angiolipomatosis Familial atypical multiple mole melanoma syndrome Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome Familial isolated trichomegaly Familial multiple lipomatosis Familial multiple trichoepithelioma Familial normophosphatemic tumoral calcinosis Familial progressive hyperpigmentation Familial reactive perforating collagenosis Familiäre multiple Naevi flammei Familiäre primäre lokalisierte kutane Amyloidose Fanconi-Anämie Farber disease Fibrofollikulom, familiäres multiples Fibrom, aponeurotisches kalzifizierendes Fibromatose, hyaline juvenile Fibromatose, superfizielle Fibrosarkom Flynn-Aird syndrome Focal acral hyperkeratosis Focal dermal hypoplasia Focal facial dermal dysplasia Focal facial dermal dysplasia type I Focal facial dermal dysplasia type II Focal facial dermal dysplasia type III Focal facial dermal dysplasia type IV Focal palmoplantar and gingival keratoderma Focal palmoplantar keratoderma Fokale Palmoplantarkeratose mit Hyperkeratose an den Gelenken Follikuläre Atrophodermie mit Basalzellkarzinom Fronto-nasale Dysplasie mit Alopezie und Genitalanomalien GAPO syndrome Gardner syndrome Gelenkhypermobilitäts-Syndrom, familiäres Generalisierte pustulöse Psoriasis Generalized basaloid follicular hamartoma syndrome Generalized eruptive keratoacanthoma Generalized peeling skin syndrome Genetic dermis elastic tissue disorder Genetic epidermal appendage anomaly Genetic hair anomaly Genetic hyperpigmentation of the skin Genetic hypopigmentation of the skin Genetic mixed dermis disorder Genetic nail anomaly Genetic photodermatosis Genetic pigmentation anomaly of the skin Genetic porokeratosis Genetic sebaceous gland anomaly Genetic skin vascular disorder Genetic subcutaneous tissue disorder Geroderma osteodysplastica Gingiva-Fibromatose-Hypertrichose-Syndrom Gorlin-Chaudhry-Moss syndrome Gorlin-Syndrom Graham Little-Piccardi-Lassueur-Syndrom Griscelli-Syndrom Griscelli-Syndrom Typ 1 Griscelli-Syndrom Typ 2 Griscelli-Syndrom Typ 3 H-Syndrom Haarschaftanomalie, isolierte Haarschaftanomalie, syndromale Haim-Munk syndrome Hair defect-photosensitivity-intellectual disability syndrome Hallermann-Streiff syndrome Harlequin ichthyosis Hartnup-Syndrom Haut, granulomatöse schlaffe Hautkrankheit, genetische, unklassifizierte Hemihyperplasie-multiples Lipomatosis-Syndrom Hereditary acrokeratotic poikiloderma Hereditary coproporphyria Hereditary hypotrichosis with recurrent skin vesicles Hereditary painful callosities Hereditary palmoplantar keratoderma, Gamborg-Nielsen type Hereditary poikiloderma Hereditäre Leiomyomatose mit Nierenzellkrebs Hereditäre fibröse Poikilodermie-Sehnenkontraktur-Myopathie-Lungenfibrose-Syndrom Hermansky-Pudlak syndrome Hermansky-Pudlak syndrome due to BLOC-2 deficiency Hermansky-Pudlak syndrome due to BLOC-3 deficiency Hermansky-Pudlak-Syndrom Typ 8 Hermansky-Pudlak-Syndrom Typ 9 Hermansky-Pudlak-Syndrom durch AP-3-Defizienz Hermansky-Pudlak-Syndrom durch BLOC-1-Defizienz Hidrotic ectodermal dysplasia Hidrotic ectodermal dysplasia, Christianson-Fourie type Hidrotic ectodermal dysplasia, Halal type Huriez-Syndrom Hutchinson-Gilford progeria syndrome Hygrom, zystisches Hyper- und Hypopigmentation, familiäre progressive Hyperkeratose-Hyperpigmentierung-Syndrom Hyperkeratosis lenticularis perstans Hypermobile Ehlers-Danlos syndrome Hypertrichose, generalisierte kongenitale, X-chromosomale Hypertrichose, pigmentierte, mit Insulin-abhängigen Diabetes mellitus-Syndrom Hypertrichose, ventrale zervikale, isolierte Hypertrichosis cubiti Hypertrichosis lanuginosa congenita Hypertrichosis-acromegaloid facial appearance syndrome Hypodontia-dysplasia of nails syndrome Hypohidrotic ectodermal dysplasia Hypohidrotic ectodermal dysplasia with immunodeficiency Hypohidrotische ektodermale Dysplasie-Hypothyreose-Ziliendyskinesie-Syndrom Hypopigmentierung-punktierte Palmoplantarkeratose-Syndrom Hypotrichose - juvenile Makuladegeneration Hypotrichose-Schwerhörigkeit-Syndrom Hypotrichosis simplex Hypotrichosis simplex des Skalps Hypotrichosis-Osteolysis-Periodontitis-Palmoplantarkeratose-Syndrom Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Hörverlust-Blindheit-Hypopigmentierung-Syndrom, jemenitischer Typ Ichthyose Ichthyose, autosomal-rezessive kongenitale Ichthyose, hereditäre Ichthyose, hereditäre, nicht-syndromale Form Ichthyose, hereditäre, syndromale Form Ichthyose, syndromale X-chromosomale Ichthyose-Alopezie-Eklabium-Ektropion-Intelligenzminderung-Syndrom Ichthyose-Syndrom, X-chromosomales Ichthyose-Syndrom, autosmales, mit prominenten Haaranomalitäten Ichthyose-Syndrom, autosomales Ichthyosis follicularis-Alopezie-Photophobie-Syndrom Ichthyosis hystrix Curth-Macklin Ichthyosis hystrix gravior Idiopathic trachyonychia IgA-Dermatose, lineare Incontinentia pigmenti Indolent primary cutaneous B-cell lymphoma Indolent primary cutaneous T-cell lymphoma Indolente systemische Mastozytose Infantile digital fibromatosis Infantile myofibromatosis Intermediate generalized junctional epidermolysis bullosa Intraepitheliale korneale Dyskeratose-palmoplantare Hyperkeratose-laryngeale Dyskeratose-Syndrom Isolated bone marrow mastocytosis Isolated congenital anonychia Isolated congenital digital clubbing Isolated congenital onychodysplasia Isolated focal palmoplantar keratoderma Isolated punctate palmoplantar keratoderma Ito hypomelanosis Johanson-Blizzard syndrome Johnson neuroectodermal syndrome Junctional epidermolysis bullosa Junctional epidermolysis bullosa inversa Junctional epidermolysis bullosa with pyloric atresia Juvenile xanthogranuloma KID-Syndrom Kardio-fazio-kutanes Syndrom Kein Name gefunden Keratinopathic ichthyosis Keratoakanthom, familiäres Keratoderma hereditarium mutilans with ichthyosis Keratoderma palmoplantaris transgrediens et progrediens Keratolytisches Winter-Erythem Keratosis follicularis spinulosa decalvans Keratosis follicularis-dwarfism-cerebral atrophy syndrome Keratosis linearis-Ichthyosis congenita-sklerosierendes Keratoderm-Syndrom Keratosis palmaris et plantaris-clinodactyly syndrome Keratosis palmoplantaris striata Keratosis pilaris rubra atrophicans Kindler epidermolysis bullosa Klassisches Ehlers-Danlos-Syndrom, ähnlich vaskulärer Typ Klippel-Trénaunay syndrome Knuckle-Pads-Leukonychie-sensorineurale Schwerhörigkeit-palmoplantare Hyperkeratose-Syndrom Kollagenom, familiäres kutanes Kongenitale generalisierte Hypertrichose Typ Ambras Kongenitaler melanozytärer Nävus, großer/riesiger Kontrakturen-ektodermale Dysplasie-Lippen-Kiefer-Gaumenspalte-Syndrom Kopfhaut-Ohr-Mamillen-Syndrom Kranio-fazio-fronto-digitales Syndrom Kraushaar-akrales Keratoderm-Karies-Syndrom Kutane Mastozytose, diffuse pseudoxanthomatöse Kyphoskoliotisches Ehlers-Danlos-Syndrom durch FKBP22-Defizienz Kyphoskoliotisches Ehlers-Danlos-Syndrom durch Lysyl-Hydroxylase 1-Mangel Kälte-Urtikaria, familiäre LMNA-related cardiocutaneous progeria syndrome LUMBAR syndrome Lacrimoauriculodentodigital syndrome Lamellar ichthyosis Laryngo-onycho-kutanes Syndrom Late-onset junctional epidermolysis bullosa Ledderhose-Krankheit Legius-Syndrom Lelis syndrome Lentiginosis, generalisierte, familiäre Form Leukoenzephalopathie - Palmoplantarkeratose Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome Leukonychia totalis Leukonychia totalis - Acanthosis-nigricans-artige Läsionen - Haarveränderungen Limb-Mammary-Syndrom Limited systemic sclerosis Linear and whorled nevoid hypermelanosis Linear atrophoderma of Moulin Linear nevus sebaceus syndrome Linear verrucous nevus syndrome Lipedema Lipoidproteinose Lipomatose, enzephalo-kranio-kutane Lipomatose, mesosomatische, Typ Roch-Leri Lipomatose, multiple symmetrische Lippen-Kiefer-Gaumen-Spalte-ektodermale Dysplasie-Syndrom Lippen-Kiefer-Gaumenspalte - ektodermale Dysplasie Localized dystrophic epidermolysis bullosa, acral form Localized dystrophic epidermolysis bullosa, nails only Localized dystrophic epidermolysis bullosa, pretibial form Localized epidermolysis bullosa simplex Localized junctional epidermolysis bullosa Loose anagen syndrome Lupus erythematodes tumidus Lupus erythematodes, diskoider Lupus erythematodes, kutaner seltener Lupus erythematodes, kutaner, subakuter Lupus erythematosus, hypertropher oder verruköser Lupus-Pannikulitis Lymphatische Malformation, makrozystische Lymphatische Malformation, mikrozystische Lymphedema Lymphoadenopathic mastocytosis with eosinophilia Lymphödem - Distichiasis Lymphödem, kongenitales primäres, nicht-hereditäres MEDNIK syndrome Maculae, hypopigmentierte und hyperpigmentierte, hereditäre kongenitale Maffucci-Syndrom Mal de Meleda Malignant atrophic papulosis Malignant melanoma of the mucosa Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome Marginal papular palmoplantar keratoderma Marie Unna hereditary hypotrichosis Marshall syndrome Mastozytom, extrakutanes Mastozytom, kutanes Mastozytose Mastozytose, bullöse diffuse kutane Mastozytose, kutane Mastozytose, kutane, diffuse Form Mastozytose, systemische, mit assoziierter hämatologischer Neoplasie Mastzell-Leukämie Mastzell-Leukämie, agressive Mastzellsarkom McCune-Albright syndrome Megalencephaly-capillary malformation-polymicrogyria syndrome Meige disease Melanom, familiäres Mikrophthalmie-lineares Hautdefekt-Syndrom Milroy-Krankheit Minimal pigment oculocutaneous albinism type 1 Monilethrix Muckle-Wells syndrome Muir-Torre syndrome Multiple benign circumferential skin creases on limbs Multiple self-healing squamous epithelioma Multiples Pterygium-Syndrom, autosomal-rezessives Mycosis fungoides and variants NEVADA syndrome Naegeli-Franceschetti-Jadassohn-Syndrom Naevus comedonicus-Syndrom Naevus verrucosus Naevus, akanthokeratolytischer verruköser Nageldysplasie, autosomal-rezessive Nagelkrankheit, isolierte Nagelkrankheit, syndromale Nail-patella syndrome Naxos-Krankheit Neonatale Haut- und Darmerkrankung, entzündliche Nestor-Guillermo progeria syndrome Netherton-Syndrom Neurocutaneous melanocytosis Neurofibromatose Typ 1 Nevus of Ito Nevus of Ota Nodular urticaria pigmentosa Non-hereditary late-onset primary lymphedema Noonan-ähnliches Syndrom mit losem Anagenhaar Occipital horn syndrome Oculocutaneous albinism Oculocutaneous albinism type 1 Oculocutaneous albinism type 1A Oculocutaneous albinism type 1B Oculocutaneous albinism type 2 Oculocutaneous albinism type 3 Oculocutaneous albinism type 4 Oculocutaneous albinism type 5 Oculocutaneous albinism type 7 Odonto-Onycho-Dysplasie mit Alopezie Odonto-tricho-ungual-digito-palmares Syndrom Odonto-trichomelisches Syndrom Odontomicronychial dysplasia Okulo-osteo-kutanes Syndrom Okulo-tricho-Dysplasie Okulozerebrales Hypopigmentierungs-Syndrom Typ Cross Oley-Syndrom Onychocytic matricoma Onychomatricoma Orofaciodigital syndrome type 1 Osteopathia striata-pigmentary dermopathy-white forelock syndrome PAPA-Syndrom PASH-Syndrom PENS-Syndrom PLEC-related intermediate epidermolysis bullosa simplex without extracutaneous involvement PTEN hamartoma tumor syndrome PYCR1-assoziiertes De Barsy-Syndrom Pachydermoperiostose Pachyonychia congenita Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome Palmoplantar keratoderma-deafness syndrome Palmoplantar keratoderma-esophageal carcinoma syndrome Palmoplantar keratoderma-spastic paralysis syndrome Palmoplantarkeratose Typ Nagashima Palmoplantarkeratose, diffuse Palmoplantarkeratose, diffuse mutilierende, autosomal-dominante Palmoplantarkeratose, hereditäre Palmoplantarkeratose, isolierte diffuse Palmoplantarkeratose, punktierte Palmoplantarkeratose, punktierte, Typ 2 Palmoplantarkeratose, punktierte, Typ I Papillon-Lefèvre syndrome Parana-Syndrom Paraneoplastic pemphigus Parkes Weber syndrome Peeling skin syndrome Pellagra-ähnliches-Syndrom Pemphigoid gestationis Pemphigus erythematosus Pemphigus foliaceus Pemphigus herpetiformis Pemphigus superficial Pemphigus vegetans Pemphigus vulgaris Pemphigus, benigner chronischer familiärer Peutz-Jeghers syndrome Phakomatosis cesioflammea Phakomatosis cesiomarmorata Phakomatosis pigmentokeratotica Phakomatosis pigmentovascularis Phakomatosis spilorosea Piebald trait-neurologic defects syndrome Piebaldism Pili bifurcati Pili gemini Pili torti Pili torti-developmental delay-neurological abnormalities syndrome Pili torti-onychodysplasia syndrome Pilodental dysplasia-refractive errors syndrome Pilomatrixoma Pityriasis rubra pilaris Plaque-form urticaria pigmentosa Poikilodermie mit Neutropenie Poikilodermie, akrokeratotische kongenitale, Typ Kindler-Weary Poikilodermie, hereditäre sklerosierende, Typ Weary Porokeratosis of Mibelli Porokeratosis plantaris palmaris et disseminata Porokeratotic eccrine ostial and dermal duct nevus Porphyria Porphyria cutanea tarda (PCT) Porphyria variegata Porphyrie durch ALA-Dehydratase-Mangel Porphyrie, akute hepatische Porphyrie, chronische hepatische Porphyrie, hepatoerythropoetische (HEP) Premature aging Primary cutaneous B-cell lymphoma Primary cutaneous T-cell lymphoma Primary cutaneous diffuse large B-cell lymphoma, leg type Primary cutaneous follicle center lymphoma Primary cutaneous gamma/delta-positive T-cell lymphoma Primary cutaneous lymphoma Primary cutaneous marginal zone B-cell lymphoma Primary cutaneous peripheral T-cell lymphoma not otherwise specified Primary lymphedema Primary non-essential cutis verticis gyrata Primär kutane CD30-positive T-Zell-Lymphoproliferation Progerie - Kleinwuchs - Pigmentnaevi Progerie-Syndrom Typ Petty Progressive osseous heteroplasia Progressive symmetric erythrokeratodermia Proteus syndrome Proteus-ähnliches Syndrom Pseudoxanthoma elasticum Pterygium-Syndrom, antekubitales Pustulosis Palmaris et Plantaris Pyramidale Molare-Oberlippenanomalie-Syndrom RIN2 syndrome Rare genetic skin disease Rare nail tumor Rare nevus Rare skin tumor or hamartoma Recessive X-linked ichthyosis Recessive aplasia cutis congenita of limbs Recessive dystrophic epidermolysis bullosa inversa Reticulate acropigmentation of Kitamura Ringed hair disease Rombo-Syndrom Rothmund-Thomson syndrome Rothmund-Thomson syndrome type 1 Rothmund-Thomson syndrome type 2 SAPHO-Syndrom SCALP syndrome SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome Scalp defects-postaxial polydactyly syndrome Schallleitungsschwerhörigkeit-Ptosis-Skelettanomalien-Syndrom Schinzel-Giedion-Syndrom Schleimhautpemphigoid Schwannomatose Schwannomatose, NF2-assoziierte Schwere Dermatitis-multiple Allergien-metabolischer Verlust-Syndrom Schwerhörigkeit-Onychodystrophie-Syndrom Schwerhörigkeit-Onychodystrophie-Syndrom, autosomal-dominantes Schwerhörigkeit-Schmelzhypoplasie-Nageldefekte-Syndrom Schöpf-Schulz-Passarge-Syndrom Scleromyxedema Sebocystomatosis Seborrhea-like dermatitis with psoriasiform elements Segmentaler Auswuchs-Lipomatose-arteriovenöse Fehlbildung-epidermaler Naevus-Syndrom Self-improving collodion baby Self-improving dystrophic epidermolysis bullosa Seltene Krankheit mit Hypertrichose Seltene lymphatische Fehlbildung Seltene systemische oder rheumatologische Krankheit Severe achondroplasia-developmental delay-acanthosis nigricans syndrome Severe generalized junctional epidermolysis bullosa Skin fragility-woolly hair-palmoplantar keratoderma syndrome Smoldering systemic mastocytosis Sparse hair-short stature-skin anomalies syndrome Spinocerebellar ataxia type 34 Spät-einsetzende lokalisierte junktionale Epidermolysis bullosa-Intelligenzminderung-Syndrom Steatocystoma multiplex-natal teeth syndrome Stiff-skin-Syndrom Subcutaneous panniculitis-like T-cell lymphoma Superficial epidermolytic ichthyosis Suprabasal epidermolysis bullosa simplex Syndrom des epidermalen Naevus Syndromic oculocutaneous albinism Syringocystadenoma papilliferum Systemic mastocytosis Systemic sclerosis Systemische Sklerose, diffuse kutane Systemische Sklerose, kutane limitierte Sézary syndrome T-Zell-Lymphom, primär kutanes, aggressives epidermotropes, CD8+ T-Zell-Lymphom, primär kutanes, klein/mittelgroßzelliges pleomorphes, CD4-+ Talgdrüsentumor, palpebraler Taurodontia-absent teeth-sparse hair syndrome Teebi-Shaltout syndrome Teleangiectasia macularis eruptiva perstans Temperature-sensitive oculocutaneous albinism type 1 Terminale Knochendysplasie - Pigmentstörungen Tietz-Syndrom Toriello-Lacassie-Droste-Syndrom Trichilemmalzyste, proliferierende Tricho-dento-ossäres Syndrom Tricho-oculo-dermo-vertebrales Syndrom Tricho-odonto-onychiale Dysplasie Tricho-retino-dento-digital syndrome Tricho-rhino-phalangeales-Syndrom Typ 2 Trichodentales Syndrom Trichodermodysplasie mit Zahnveränderungen Trichodysplasia-amelogenesis imperfecta syndrome Trichodysplasie-Xerodermie-Syndrom Trichofolliculoma Trichomegalie - retinale Pigmentdegeneration - Kleinwuchs Trichorhinophalangeal syndrome Trichorhinophalangeal syndrome type 1 Trichothiodystrophie Tumorale Kalzinose, familiäre Typical urticaria pigmentosa Tyrosinemia type 2 UV-sensitives Syndrom Ulerythema ophryogenesis Unclassified genetic skin disorder Uncombable hair syndrome Undifferenzierte Kollagenosen Uroporphyrie, erythropoetische, mit assoziierter myeloischer Neoplasie Urticaria pigmentosa Van den Bosch syndrome Vascular Ehlers-Danlos syndrome Vici-Syndrom Waardenburg syndrome Waardenburg-Syndrom Typ 1 Waardenburg-Syndrom Typ 2 Waardenburg-Syndrom Typ 3 Werner-Syndrom Werner-Syndrom, atypisches White sponge nevus Wiedemann-Rautenstrauch syndrome Woolly hair Woolly hair nevus Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome X-chromosomale retikuläre Pigmentierungsstörung X-linked hypohidrotic ectodermal dysplasia Xeroderma pigmentosum Xeroderma pigmentosum variant Xeroderma pigmentosum-Cockayne syndrome complex Zahn-Nagel-Syndrom Typ Fried Zerebelläre Ataxie - ektodermale Dysplasie Zylindromatose, familiäre