SE-ATLAS

ADULT syndrome ALDH18A1-related De Barsy syndrome AREDYLD syndrome Absence of fingerprints-congenital milia syndrome Acquired ichthyosis Acral peeling skin syndrome Acral self-healing collodion baby Acrodermatitis continua suppurativa Hallopeau Acrogeria Acrokeratoelastoidosis of Costa Acrokeratosis verruciformis of Hopf Acroosteolysis-keloid-like lesions-premature aging syndrome Acute intermittent porphyria Adulte T-Zell-Leukämie/Lymphom Aggressive primary cutaneous B-cell lymphoma Aggressive primary cutaneous T-cell lymphoma Akrokeratodermie, genetisch bedingte Albinism-deafness syndrome 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-hypohidrotic syndrome Amelocerebrohypohidrotic syndrome Anetodermie, familiäre Angiolipomatose familiale Angioosteohypertrophic syndrome Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Ankyloblepharon-ektodermale Defekte-Lippen-Kiefer-Gaumenspalte-Syndrom Annular epidermolytic ichthyosis Anomalie génétique de la pigmentation cutanée Anomalie génétique des cheveux Anomalie génétique des glandes sébacées Anomalie génétique des ongles Anomalie génétique des phanères 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 syndrome Ataxia-Teleangiectasia Atrichia with papular lesions Atrophodermia vermiculata Autosomal dominant cutis laxa Autosomal dominant diffuse mutilating palmoplantar keratoderma Autosomal dominant disease associated with punctate 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 hypohidrotic ectodermal dysplasia Autosomal dominant palmoplantar keratoderma and congenital alopecia Autosomal erythropoietic protoporphyria Autosomal recessive cutis laxa type 1 Autosomal recessive cutis laxa type 2 Autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature 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-dominante Tricho-Odonto-Onycho-Dysplasie - Syndaktylie Autosomal-rezessive Krankheit mit diffuser Palmoplantarkeratose als Hauptmerkmal B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome Bannayan-Riley-Ruvalcaba-Syndrom 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 Brittle cornea syndrome Brooke-Spiegler-Syndrom Bullous pemphigoid Buschke-Ollendorff syndrome Bébé collodion à guérison spontanée Böök syndrome CEDNIK syndrome CHIME syndrome CLAPO-Syndrom CLOVES syndrome COFS-Syndrom Cardiac-valvular Ehlers-Danlos syndrome Carney-Komplex Cartilage-hair hypoplasia Carvajal-Syndrom Cerebellar ataxia-ectodermal dysplasia syndrome Cervical hypertrichosis-peripheral neuropathy syndrome Chilblain-Lupus Chondrodysplasia punctata, X-chromosomal-dominante Chondroectodermal dysplasia with night blindness Choroidal atrophy-alopecia syndrome Chédiak-Higashi syndrome Classic mast cell leukemia Classical-like Ehlers-Danlos syndrome type 1 Cleft lip/palate-ectodermal dysplasia syndrome Cockayne syndrome Cockayne syndrome type 1 Cockayne syndrome type 2 Cockayne syndrome type 3 Congenital erythropoietic porphyria Congenital generalized hypertrichosis, Ambras type Congenital lethal erythroderma Congenital panfollicular nevus Congenital reticular ichthyosiform erythroderma Congenital smooth muscle hamartoma Cooks-Syndrom Corneodermatoosseous syndrome Cowden syndrome Crandall syndrome Craniofaciofrontodigital syndrome Cronkhite-Canada syndrome Curly hair-acral keratoderma-caries syndrome Cutaneous mastocytoma 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 disease De Barsy-Syndrom Deaf blind hypopigmentation syndrome, Yemenite type Deafness-enamel hypoplasia-nail defects syndrome Dermatite bulleuse auto-immune Dermatitis herpetiformis Dermatofibrosarcome de Darier-Ferrand Dermatomyositis Dermatoosteolysis, Kirghizian type Dermatopathia pigmentosa reticularis Dermochondrocorneal dystrophy Dermoodontodysplasia Dermotrichales Syndrom Didymosis aplasticosebacea Diffuse Palmoplantarkeratose mit schmerzhaften Fissuren Diffuse cutaneous mastocytosis Diffuse lymphatic malformation Diffuse palmoplantar keratoderma, Bothnian type Diffuse palmoplantar keratoderma-acrocyanosis syndrome 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 Dyskératose congénitale Dysostose acrofaciale type Weyers Dysplasie cranio-ectodermique Dysplasie, ektodermale hypohidrotische, autosomal-rezessive Dysplasie, odonto-onycho-dermale Dysplasie, okulo-dento-digitale Dystrophic epidermolysis bullosa Dystrophie, bullöse, hereditäre, makulärer Typ EEC-Syndrom EEM-Syndrom Ectodermal dysplasia with natal teeth, Turnpenny type Ectodermal dysplasia, trichoodontoonychial type Ectodermal dysplasia-blindness syndrome Ectodermal dysplasia-intellectual disability-central nervous system malformation 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 syndrome, fibronectinemic type Ehlers-Danlos-Syndrom, Arthrochalasie-Typ Ehlers-Danlos-Syndrom, Dermatosparaxis Typ Ehlers-Danlos-Syndrom, muskulo-kontrakturaler Typ Ehlers-Danlos-Syndrom, parodontaler Typ Ehlers-Danlos/osteogenesis imperfecta syndrome Ektodermale Dysplasie Ektodermale Dysplasie-sensorineurale Schwerhörigkeit-Syndrom Encephalocraniocutaneous lipomatosis Epidermal nevus syndrome Epidermale Krankheit, genetisch bedingte Epidermalnaevus, inflammatorischer lineärer verruköser Epidermolyse bulleuse simple avec anodontie/hypodontie Epidermolyse bulleuse simple généralisée autosomique dominante, forme sévère Epidermolyse bulleuse simple par déficit en BP230 Epidermolysis bullosa simplex Epidermolysis bullosa simplex due to exophilin 5 deficiency Epidermolysis bullosa simplex mit Muskeldystrophie Epidermolysis bullosa simplex superficialis 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, 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 Epithéliome squameux multiple spontanément curable Erythema palmare hereditarium Erythrodermie congénitale ichtyosiforme Erythrokeratoderma ''en cocardes Erythrokeratoderma variabilis progressiva Erythrokeratodermia variabilis Erythrokeratodermie, genetisch bedingte Erythromelalgia Exfoliative ichthyosis Familial atypical multiple mole melanoma syndrome Familial cylindromatosis Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome Familial isolated trichomegaly Familial keratoacanthoma Familial melanoma Familial multiple fibrofolliculoma Familial multiple nevi flammei Familial multiple trichoepithelioma Familial normophosphatemic tumoral calcinosis Familial progressive hyper- and hypopigmentation Familial progressive hyperpigmentation Familial reactive perforating collagenosis Familiäre primäre lokalisierte kutane Amyloidose Fanconi-Anämie Farber disease Fibrom, aponeurotisches kalzifizierendes Fibromatose digitale infantile Fibromatose, hyaline juvenile Fibromatose, superfizielle Fibrosarkom 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 Fokale Palmoplantarkeratose mit Hyperkeratose an den Gelenken Follicular atrophoderma-basal cell carcinoma Frontonasal dysplasia-alopecia-genital anomalies syndrome GAPO syndrome Gelenkhypermobilitäts-Syndrom, familiäres Generalisierte pustulöse Psoriasis Generalized basaloid follicular hamartoma syndrome Generalized peeling skin syndrome Genetic dermis elastic tissue disorder Genetic hyperpigmentation of the skin Genetic hypopigmentation of the skin Genetic mixed dermis disorder Genetic photodermatosis 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 disease Haut, granulomatöse schlaffe Hautkrankheit, genetische, unklassifizierte Hemihyperplasia-multiple lipomatosis syndrome Hereditary acrokeratotic poikiloderma Hereditary acrokeratotic poikiloderma of Kindler-Weary Hereditary coproporphyria Hereditary painful callosities Hereditary palmoplantar keratoderma, Gamborg-Nielsen type Hereditary poikiloderma Hereditary sclerosing poikiloderma, Weary type Hereditäre Leiomyomatose mit Nierenzellkrebs Hereditäre fibröse Poikilodermie-Sehnenkontraktur-Myopathie-Lungenfibrose-Syndrom Hermansky-Pudlak syndrome Hermansky-Pudlak syndrome due to BLOC-1 deficiency Hermansky-Pudlak syndrome due to BLOC-2 deficiency Hermansky-Pudlak syndrome due to BLOC-3 deficiency Hermansky-Pudlak syndrome type 8 Hermansky-Pudlak-Syndrom Typ 9 Hermansky-Pudlak-Syndrom durch AP-3-Defizienz Hidrotic ectodermal dysplasia Hidrotic ectodermal dysplasia, Christianson-Fourie type Hidrotic ectodermal dysplasia, Halal type Huriez-Syndrom Hutchinson-Gilford progeria syndrome Hygrom, zystisches Hyperkeratose-Hyperpigmentierung-Syndrom Hyperkératose lenticulaire persistante Hypertrichose, generalisierte kongenitale, X-chromosomale Hypertrichose, ventrale zervikale, isolierte Hypertrichosis cubiti Hypertrichosis lanuginosa congenita Hypodontia-dysplasia of nails syndrome Hypohidrotic ectodermal dysplasia Hypohidrotic ectodermal dysplasia with immunodeficiency Hypohidrotische ektodermale Dysplasie-Hypothyreose-Ziliendyskinesie-Syndrom Hypopigmentation-punctate palmoplantar keratoderma syndrome Hypotrichose héréditaire à vésicules cutanées récidivantes Hypotrichose simple Hypotrichose-Schwerhörigkeit-Syndrom Hypotrichosis simplex of the scalp Hypotrichosis with juvenile macular degeneration Hypotrichosis-Osteolysis-Periodontitis-Palmoplantarkeratose-Syndrom Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome 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 Ichtyose kératinopathique Ichtyose syndromique autosomique avec d'autres signes associés Ichtyose syndromique autosomique avec signes neurologiques prédominants Ichtyose syndromique autosomique avec évolution fatale de la maladie Idiopathic trachyonychia IgA-Dermatose, lineare Incontinentia pigmenti Indolent primary cutaneous B-cell lymphoma Indolente systemische Mastozytose 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 punctate palmoplantar keratoderma Ito hypomelanosis Junctional epidermolysis bullosa Junctional epidermolysis bullosa inversa Junctional epidermolysis bullosa with pyloric atresia Juvenile xanthogranuloma KID syndrome Kardio-fazio-kutanes Syndrom Kein Name gefunden Keratoderma hereditarium mutilans with ichthyosis Keratoderma palmoplantaris transgrediens et progrediens Keratolytic winter erythema Keratosis follicularis spinulosa decalvans Keratosis follicularis-dwarfism-cerebral atrophy syndrome Keratosis linearis-Ichthyosis congenita-sklerosierendes Keratoderm-Syndrom Keratosis palmaris et plantaris-clinodactyly syndrome Keratosis pilaris rubra atrophicans Kindler epidermolysis bullosa Knuckle-Pads-Leukonychie-sensorineurale Schwerhörigkeit-palmoplantare Hyperkeratose-Syndrom Kollagenom, familiäres kutanes Kontrakturen-ektodermale Dysplasie-Lippen-Kiefer-Gaumenspalte-Syndrom Kopfhaut-Ohr-Mamillen-Syndrom Kutane Mastozytose, diffuse pseudoxanthomatöse Kyphoskoliotisches Ehlers-Danlos-Syndrom durch FKBP22-Defizienz Kyphoskoliotisches Ehlers-Danlos-Syndrom durch Lysyl-Hydroxylase 1-Mangel Kälte-Urtikaria, familiäre Kératoacanthome éruptif généralisé Kératodermie palmoplantaire diffuse isolée autosomique dominante Kératodermie palmoplantaire et alopécie congénitale autosomique récessive Kératodermie palmoplantaire focale Kératodermie palmoplantaire focale isolée LUMBAR syndrome Lacrimoauriculodentodigital syndrome Lamellar ichthyosis Large congenital melanocytic nevus Laryngo-onycho-kutanes Syndrom Late-onset junctional epidermolysis bullosa Ledderhose-Krankheit Legius-Syndrom Lelis syndrome Lentiginosis, generalisierte, familiäre Form Lethal acantholytic erosive disorder Leukoencephalopathy-palmoplantar keratoderma syndrome Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome Leukonychia totalis Leukonychia totalis - Acanthosis-nigricans-artige Läsionen - Haarveränderungen Limb-mammary syndrome Linear and whorled nevoid hypermelanosis Linear atrophoderma of Moulin Linear nevus sebaceus syndrome Linear verrucous nevus syndrome Lipedema Lipoidproteinose Lipomatose multiple familiale Lipomatose, mesosomatische, Typ Roch-Leri Lippen-Kiefer-Gaumen-Spalte-ektodermale Dysplasie-Syndrom 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 érythémateux cutané chronique Lupus-Pannikulitis Lymphatische Malformation, makrozystische Lymphatische Malformation, mikrozystische Lymphoadenopathic mastocytosis with eosinophilia Lymphoedème Lymphome B cutané de la zone marginale Lymphome NK/T extranodulaire type nasal Lymphome T cutané primitif d'évolution indolente Lymphome T cutané primitif de phénotype TCRgamma/delta Lymphome T sous-cutané type panniculite Lymphome cutané primitif Lymphome cutané primitif à cellules T périphérique sans autre indication Lymphome cutané à grandes cellules de type jambe Lymphomes B centrofolliculaire cutané primitif Lymphödem - Distichiasis Maculae, hypopigmentierte und hyperpigmentierte, hereditäre kongenitale Maculopapular cutaneous mastocytosis Maffucci-Syndrom Mal de Meleda Maladie autosomique dominante avec kératodermie palmoplantaire diffuse comme manifestation majeure Maladie autosomique dominante avec une kératodermie palmoplantaire focale comme manifestation majeure Maladie avec une kératodermie palmoplantaire diffuse comme manifestation majeure Maladie dermatologique rare d'origine génétique Maladie génétique non classifiée de la peau Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome Marginal papular palmoplantar keratoderma Marie Unna hereditary hypotrichosis Mastocytose systémique Mastocytose systémique type smoldering Mastozytom, extrakutanes Mastozytose Mastozytose, bullöse diffuse kutane Mastozytose, kutane Mastozytose, systemische, mit assoziierter hämatologischer Neoplasie Mastzell-Leukämie Mastzell-Leukämie, agressive Mastzellsarkom McCune-Albright syndrome Megalencephaly-capillary malformation-polymicrogyria syndrome Meige disease Mikrophthalmie-lineares Hautdefekt-Syndrom Milroy disease Minimal pigment oculocutaneous albinism type 1 Monilethrix Muckle-Wells syndrome Muir-Torre syndrome Multiple benign circumferential skin creases on limbs Multiple symmetric lipomatosis Multiples Pterygium-Syndrom, autosomal-rezessives Mycosis fungoides and variants Myofibromatose infantile Mélanome malin muqueux NEVADA syndrome Naegeli-Franceschetti-Jadassohn syndrome Naevus blanc spongieux Naevus comedonicus-Syndrom Naevus rare Naevus verrucosus Naevus, akanthokeratolytischer verruköser Nageldysplasie, autosomal-rezessive Nagelkrankheit, isolierte Nagelkrankheit, syndromale Nail-patella syndrome Naxos-Krankheit Neonatale Haut- und Darmerkrankung, entzündliche Netherton-Syndrom Neurocutaneous melanocytosis Neurofibromatose Typ 1 Nevus of Ito Nevus of Ota Non-hereditary congenital primary lymphedema 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 6 Oculocutaneous albinism type 7 Odonto-Onycho-Dysplasie mit Alopezie Odonto-tricho-ungual-digito-palmar syndrome Odonto-trichomelisches Syndrom Odontomicronychial dysplasia Okulo-osteo-kutanes Syndrom Okulo-tricho-Dysplasie Okulozerebrales Hypopigmentierungs-Syndrom Typ Cross Oley syndrome 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 Pachydermoperiostosis Pachyonychia congenita Palmoplantar keratoderma, Nagashima type Palmoplantar keratoderma-deafness syndrome Palmoplantar keratoderma-spastic paralysis syndrome Palmoplantarkeratose, diffuse Palmoplantarkeratose, hereditäre Palmoplantarkeratose, isolierte diffuse Palmoplantarkeratose, punktierte Palmoplantarkeratose, punktierte, Typ 2 Palmoplantarkeratose, punktierte, Typ I Papulose atrophiante maligne Parana hard skin syndrome Paraneoplastic pemphigus Peeling skin syndrome Pellagra-ähnliches-Syndrom Pemphigoid gestationis Pemphigus erythematosus Pemphigus foliaceus Pemphigus herpetiformis Pemphigus superficial Pemphigus vegetans Pemphigus vulgaris Pemphigus, benigner chronischer familiärer Phacomatose pigmento-kératosique Phacomatose pigmento-vasculaire Phakomatosis cesioflammea Phakomatosis cesiomarmorata Phakomatosis spilorosea Piebald trait-neurologic defects syndrome Piebaldism Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome 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 Poikilodermie mit Neutropenie Porokeratosis of Mibelli Porokeratosis plantaris palmaris et disseminata Porokeratotic eccrine ostial and dermal duct nevus Porokératose génétique Porphyria Porphyria cutanea tarda (PCT) Porphyria variegata Porphyrie durch ALA-Dehydratase-Mangel Porphyrie, akute hepatische Porphyrie, chronische hepatische Porphyrie, hepatoerythropoetische (HEP) Primary cutaneous B-cell lymphoma Primary cutaneous T-cell lymphoma 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 Progéria de Nestor-Guillermo Proliferating trichilemmal cyst Proteus syndrome Proteus-ähnliches Syndrom Pseudoxanthoma elasticum Pterygium-Syndrom, antekubitales Pure hair and nail ectodermal dysplasia Pustulosis Palmaris et Plantaris Pyramidale Molare-Oberlippenanomalie-Syndrom RIN2 syndrome Rare nail tumor 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 Schöpf-Schulz-Passarge syndrome Sclérodermie systémique Scléromyxoedème Sclérose systémique limitée Sebocystomatosis Seborrhea-like dermatitis with psoriasiform elements Segmentaler Auswuchs-Lipomatose-arteriovenöse Fehlbildung-epidermaler Naevus-Syndrom 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 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 Striate palmoplantar keratoderma Superficial epidermolytic ichthyosis Suprabasal epidermolysis bullosa simplex Syndrome ANE Syndrome CHILD Syndrome CREST Syndrome EEC et maladies associées Syndrome FLOTCH Syndrome MEDNIK Syndrome cerveau-poumon-thyroïde Syndrome d'Ehlers-Danlos classique Syndrome d'Ehlers-Danlos hypermobile Syndrome d'Ehlers-Danlos vasculaire Syndrome d'Ellis-Van Creveld Syndrome d'acanthosis nigricans-résistance à l'insuline-crampes-hypertrophie acrale Syndrome d'hypertrichose-faciès acromégaloïde Syndrome d'oligodontie-taurodontie-cheveux rares Syndrome de Barber-Say Syndrome de Bartsocas-Papas Syndrome de Flynn-Aird Syndrome de Gardner Syndrome de Johanson-Blizzard Syndrome de Klippel-Trénaunay Syndrome de Marshall Syndrome de Papillon-Lefèvre Syndrome de Parkes Weber Syndrome de Peutz-Jeghers Syndrome de Schauder Syndrome de Van der Bosch Syndrome de cataracte-hypertrichose-déficience intellectuelle Syndrome de dysplasie ectodermique-hyperhidrose-syndactylie cutanée Syndrome de dysplasie ectodermique-pili torti-syndactylie cutanée Syndrome de kératodermie palmoplantaire-ambiguïté sexuelle XX-prédisposition au carcinome spinocellulaire Syndrome de kératodermie palmoplantaire-carcinome de l'oesophage Syndrome des ptérygiums multiples autosomique dominant Syndrome neuroectodermique de Johnson Syndrome progéroïde cardio-cutané lié à LMNA Syndromic oculocutaneous albinism Syringocystadenoma papilliferum 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 Teebi-Shaltout syndrome Teleangiectasia macularis eruptiva perstans Temperature-sensitive oculocutaneous albinism type 1 Terminale Knochendysplasie - Pigmentstörungen Tietz-Syndrom Toriello-Lacassie-Droste syndrome Tricho-dento-osseous syndrome Tricho-oculo-dermo-vertebral syndrome Tricho-retino-dento-digital syndrome Tricho-rhino-phalangeales-Syndrom Typ 2 Trichodental syndrome Trichodermodysplasia-dental alterations syndrome Trichodysplasia-amelogenesis imperfecta syndrome Trichodysplasie-Xerodermie-Syndrom Trichofolliculoma Trichomegalie - retinale Pigmentdegeneration - Kleinwuchs Trichoodontoonychial dysplasia Trichorhinophalangeal syndrome Trichorhinophalangeal syndrome type 1 Trichothiodystrophy Tumeur ou hamartome de la peau Tumorale Kalzinose, familiäre Tyrosinémie type 2 Télangiectasie cutanée familiale et syndrome de prédisposition au cancer oropharyngé UV-sensitive syndrome Ulérythème ophryogène Uncombable hair syndrome Undifferenzierte Kollagenosen Uroporphyrie, erythropoetische, mit assoziierter myeloischer Neoplasie Urticaire pigmentaire en plaques Urticaire pigmentaire nodulaire Urticaire pigmentaire typique Vascular-like classical Ehlers-Danlos syndrome Vici-Syndrom Vieillissement prématuré Waardenburg syndrome Waardenburg syndrome type 1 Waardenburg syndrome type 2 Waardenburg syndrome type 3 Werner syndrome Werner-Syndrom, atypisches Wiedemann-Rautenstrauch syndrome Woolly hair Woolly hair nevus Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome X-linked Ehlers-Danlos syndrome X-linked hypohidrotic ectodermal dysplasia X-linked reticulate pigmentary disorder Xeroderma pigmentosum Xeroderma pigmentosum variant Xeroderma pigmentosum-Cockayne syndrome complex Zahn-Nagel-Syndrom Typ Fried