SE-ATLAS

Johanson-Blizzard syndrome Hereditary hypotrichosis with recurrent skin vesicles Ulerythema ophryogenesis Keratinopathic ichthyosis Papillon-Lefèvre syndrome Chronic cutaneous lupus erythematosus MEDNIK syndrome Primary cutaneous lymphoma Extranodal nasal NK/T cell lymphoma Primary cutaneous marginal zone B-cell lymphoma Malignant atrophic papulosis Acrofacial dysostosis, Weyers type Johnson neuroectodermal syndrome Infantile digital fibromatosis Focal palmoplantar keratoderma Limited systemic sclerosis Autosomal ichthyosis syndrome with fatal disease course Brain-lung-thyroid syndrome CREST syndrome Peeling skin syndrome Ectodermal dysplasia-pili torti-cutaneous syndactyly syndrome Genetic porokeratosis EEC syndrome and related disorders FLOTCH syndrome Primary cutaneous gamma/delta-positive T-cell lymphoma Infantile myofibromatosis Hyperkeratosis lenticularis perstans Ectodermal dysplasia-hyperhidrosis-cutaneous syndactyly syndrome Primary cutaneous follicle center lymphoma Genetic hair anomaly Flynn-Aird syndrome Systemic sclerosis Rare nevus Autosomal recessive palmoplantar keratoderma and congenital alopecia Dyskeratosis congenita Genetic epidermal appendage anomaly Lymphedema CHILD syndrome Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome Taurodontia-absent teeth-sparse hair syndrome Primary cutaneous peripheral T-cell lymphoma not otherwise specified Autosomal dominant multiple pterygium syndrome Barber-Say syndrome Autosomal ichthyosis syndrome with prominent neurologic signs LMNA-related cardiocutaneous progeria syndrome Subcutaneous panniculitis-like T-cell lymphoma Typical urticaria pigmentosa White sponge nevus Peutz-Jeghers syndrome Rare skin tumor or hamartoma Hypotrichosis simplex Familial multiple lipomatosis Angora hair nevus Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome Genetic nail anomaly Epidermolysis bullosa simplex with anodontia/hypodontia Primary cutaneous diffuse large B-cell lymphoma, leg type Unclassified genetic skin disorder Bartsocas-Papas syndrome Isolated focal palmoplantar keratoderma Generalized eruptive keratoacanthoma Van den Bosch syndrome Multiple self-healing squamous epithelioma Disease with diffuse palmoplantar keratoderma as a major feature Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome Familial angiolipomatosis Tyrosinemia type 2 Autosomal ichthyosis syndrome with other associated signs Phakomatosis pigmentokeratotica Nodular urticaria pigmentosa Premature aging Indolent primary cutaneous T-cell lymphoma Phakomatosis pigmentovascularis Cataract-hypertrichosis-intellectual disability syndrome Hypertrichosis-acromegaloid facial appearance syndrome Gardner syndrome Palmoplantarkeratose, autosomal-dominante, isolierte diffuse Mastozytose, systemische Urtikaria pigmentosa, plaqueförmige Ehlers-Danlos-Syndrom, hypermobiler Typ Epidermolysis bullosa simplex durch BP230-Mangel Malignes Melanom der Mukosa Skleromyxödem Hautkrankheit, seltene, genetisch bedingte Autosomal-dominante Krankheit mit assoziierter diffuser Palmoplantarkeratose als Hauptmerkmal Ehlers-Danlos-Syndrom, vaskulärer Typ Erythrodermie, ichthyosiforme kongenitale Schwelende systemische Mastozytose Pigmentanomalien der Haut, genetisch bedingte Ehlers-Danlos-Syndrom, klassischer Typ Dermatofibrosarcoma protuberans Marshall-Syndrom Nestor-Guillermo-Progeroid-Syndrom Dysplasie, kranioektodermale Kein Name gefunden Talgdrüsenanomalie, genetisch bedingte Parkes-Weber-Syndrom ANE-Syndrom Epidermolysis bullosa simplex, generalisierte schwere Selbstheilendes Kollodium-Baby Palmoplantarkeratose - Ösophageales Karzinom Klippel-Trénaunay-Syndrom Hautkrankheit, autoimmune bullöse Ellis Van Creveld-Syndrom Autosomal-dominante Krankheit mit assoziierter fokaler Palmoplantarkeratose als Hauptmerkmal Primär kutanes T-Zell-Lymphom, aggressives Keratoderma hereditarium mutilans mit Ichthyose McCune-Albright-Syndrom Epidermolytische palmoplantare Keratose Hyperpigmentierung der Haut, genetisch bedingte Epidermolysis bullosa simplex durch Exophilin 5-Mangel Teebi-Shaltout-Syndrom Autosomal-rezessive Krankheit mit fokaler Palmoplantarkeratose als Hauptmerkmal Fokale palmoplantare und gingivale Keratose Alopecia totalis Diffuse Palmoplantarkeratose vom Bottnischen Typ Primär kutanes B-Zell-Lymphom, indolentes Epidermolysis bullosa simplex mit gesprenkelter Pigmentierung Palmoplantarkeratose-spastische Paralyse-Syndrom Palmoplantarkeratose, autosomal-rezessive, isolierte diffuse Ehlers-Danlos-Syndrom Typ 1 Palmoplantarkeratose, isolierte punktierte Epidermolysis bullosa simplex, lokalisierte Dermatitis herpetiformis Alopecia universalis Palmoplantarkeratose-Schwerhörigkeit-Syndrom Primär kutanes B-Zell-Lymphom, aggressives Syndrom des linearen verrukösen Naevus Piebaldismus Primäre Cutis verticis gyrata, nicht-essentielle PLEC-assoziierte intermediäre Epidermolysis bullosa simplex ohne extrakutane Beteiligung Mastozytose des Knochenmarks, isolierte Keratosis follicularis-Kleinwuchs-Hirnatrophie-Syndrom Didymosis aplasticosebacea Dermato-Osteolyse, kirgisischer Typ Epidermolysis bullosa simplex, generalisierte intermediäre, autosomal-dominante Syndrom des linearen Naevus sebaceus GAPO-Syndrom LUMBAR-Syndrom Piebaldismus - neurologische Anomalien Tricho-rhino-phalangeales Syndrom Keratosis follicularis spinulosa decalvans Fehlende Dermatoglyphen-kongenitale Milien-Syndrom Pemphigoid, bullöses Okulokutaner Albinismus, syndromaler SLC39A13-assoziiertes spondylodysplastisches Ehlers-Danlos-Syndrom Syringocystadenoma papilliferum Oro-fazio-digitales Syndrom Typ 1 Pemphigus vulgaris Junktionale Epidermolysis bullosa mit Pylorusatresie Aplasia cutis congenita PTEN-Hamartom-Tumor-Syndrom Nagel-Patella-Syndrom Sebozystomatose Trichodysplasie - Amelogenesis imperfecta Albinismus, okulokutaner , Typ 1, minimal-pigmentierter Ichthyose, exfoliative ADULT-Syndrom Haim-Munk-Syndrom Ostiumnaevus, ekkriner porokeratotischer Epidermolysis bullosa, junktionale lokalisierte Epidermolysis bullosa, junktionale, generalisierte intermediäre Dermoodontodysplasie Aplasia cutis congenita der Gliedmaßen, rezessive Xeroderma pigmentosum/Cockayne-Syndrom-Komplex Schütteres Haar - Kleinwuchs - Hautveränderungen Albinismus, okulokutaner, Typ 1, temperaturempfindlicher Epidermolysis bullosa inversa, junktionale Naevus, panfollikulärer, kongenitaler NEVADA-Syndrom Aplasia cutis congenita mit intestinaler Lymphangiektasie Sézary-Syndrom Pili torti Hypopigmentierung der Haut, genetisch bedingte Epidermolysis bullosa, junctionale, generalisierte schwere Ehlers-Danlos-Syndrom Typ 2 Hypomelanose Typ Ito Pili torti-Onychodysplasie-Syndrom Aplasia cutis congenita-Myopie-Syndrom Trichomegalie, isolierte, familiäre Form SCALP-Syndrom Melanozytose, neurokutane Albinismus, okulokutaner, Typ 1 Pili torti - Entwicklungsverzögerung - neurologische Anomalien Dysplasie, dermale faziale fokale, Typ I Epidermolysis bullosa, junktionale, spät beginnende Hyperlaxität der Haut durch Mangel an Vitamin K-abhängigen Koagulationsfaktoren Angio-osteo-hypertrophisches Syndrom Monilethrix Dysplasie, pilo-dentale - Refraktionsanomalien Palmoplantarkeratose, marginale papulöse Epidermolysis bullosa inversa, dystrophe, rezessive Megalenzephalie-Kapillarfehlbildungen-Polymikrogyrie-Syndrom Seborrhö-ähnliche Dermatitis mit psoriasiformen Ausschlägen Koproporphyrie, hereditäre Selbstheilendes Kollodiumbaby, akrales Familiäres atpisches multiples Muttermal- und Melanomsyndrom Peeling-Skin-Syndrom, lokalisiertes Primär kutanes B-Zell-Lymphom Epidermolysis bullosa, dystrophe, generalisierte schwere, autosomal-rezessive Muckle-Wells-Syndrom Meige-Krankheit Cockayne-Syndrom Typ 2 Epidermolysis bullosa, dystrophe Epidermolysis bullosa, dystrophe, selbstheilende Form Chédiak-Higashi-Syndrom Pilomatrixom Waardenburg-Syndrom Epidermolysis bullosa simplex Epidermolysis bullosa, dystrophe lokalisierte, prätibiale Form Genetischer Defekt des elastischen Hautgewebes Lose Anagenhaar-Syndrom Cockayne-Syndrom Typ 1 Krankheit mit fokaler Palmoplantarkeratose als Hauptmerkmal Lymphödem primäres, mit spätem Beginn, nicht-hereditär Mastozytose, lymphoadenopathische, mit Eosinophilie Geroderma osteodysplastica Karzinom, kutanes neuroendokrines Epidermolysis bullosa, junktionale Ringelhaare Mycosis fungoides-Varianten Porphyrie, erythropoetische kongenitale Ichthyose, anuläre epidermolytische Hautschwielen, hereditäre schmerzhafte Dysplasie, ektodermale - Blindheit Pityriasis rubra pilaris Hautkrankheit, vaskuläre, genetisch bedingte Wollhaare Cockayne-Syndrom Typ 3 Porphyrie, akute intermittierende Ehlers-Danlos-Syndrom mit periventrikulärer Heterotopie Dysplasie, dermale faziale fokale, Typ III Mastzellleukämie, klassische Albinismus, okulokutaner, Typ 7 Heteroplasie, progressive ossäre Pemphigus, paraneoplastischer Book-Syndrom Poikilodermie, hereditäre Anonychie, isolierte kongenitale Hypotrichose, hereditäre kongenitale, Typ Marie Unna Dysplasie, ektodermale hidrotische, Typ Christianson-Fourie Wollhaarnaevus Mandibuläre Hypoplasie-Schwerhörigkeit-Progeroide Merkmale-Lipodystrophie-Syndrom Hypertrichose der Hals-Vorderseite - periphere Neuropathie Gewebekrankheit, subkutane, genetisch bedingte Protoporphyrie, erythropoetische, autosomale Form Dysplasie, ektodermale hidrotische, Typ Halal Dermale Krankheit, gemischte, genetisch bedingte Ehlers-Danlos-Syndrom Typ 7B Epidermolysis bullosa simplex, suprabasale Tricho-retino-dento-digitales Syndrom Dowling-Degos-Krankheit Keratosis palmaris et plantaris - Klinodaktylie Amelo-zerebro-hypohidrotisches Syndrom Autosomal dominant hypohidrotic ectodermal dysplasia Generalized peeling skin syndrome Ehlers-Danlos syndrome type 7A Hypertrichosis cubiti Odontomicronychial dysplasia Acrokeratoelastoidosis of Costa Onychocytic matricoma Pili bifurcati Diffuse palmoplantar keratoderma-acrocyanosis syndrome Cartilage-hair hypoplasia Isolated congenital onychodysplasia Linear atrophoderma of Moulin Familial reactive perforating collagenosis Autosomal dominant epidermolytic ichthyosis Ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome Anonychia congenita totalis Hypertrichosis lanuginosa congenita Dermatopathia pigmentosa reticularis Basal epidermolysis bullosa simplex Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Familial progressive hyperpigmentation Lamellar ichthyosis Rare nail tumor Dyschromatosis symmetrica hereditaria Acroosteolysis-keloid-like lesions-premature aging syndrome Dermochondrocorneal dystrophy Hereditary palmoplantar keratoderma, Gamborg-Nielsen type Primary lymphedema Muir-Torre syndrome AREDYLD syndrome Aleukemic mast cell leukemia Erythrokeratoderma ''en cocardes Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome Hereditary acrokeratotic poikiloderma Ectodermal dysplasia-skin fragility syndrome Acrokeratosis verruciformis of Hopf Progressive symmetric erythrokeratodermia Albinism-deafness syndrome Focal facial dermal dysplasia Kindler epidermolysis bullosa Linear and whorled nevoid hypermelanosis Erythrokeratodermia variabilis Hair defect-photosensitivity-intellectual disability syndrome Chondroectodermal dysplasia with night blindness X-linked hypohidrotic ectodermal dysplasia Lacrimoauriculodentodigital syndrome Congenital lethal erythroderma Hermansky-Pudlak syndrome due to BLOC-3 deficiency Woolly hair-hypotrichosis-everted lower lip-outstanding ears syndrome Acrogeria Acquired ichthyosis Bathing suit ichthyosis Ectodermal dysplasia, trichoodontoonychial type Rothmund-Thomson syndrome Reticulate acropigmentation of Kitamura Idiopathic trachyonychia Wiedemann-Rautenstrauch syndrome Focal acral hyperkeratosis Trichofolliculoma Spinocerebellar ataxia type 34 Hypodontia-dysplasia of nails syndrome Superficial epidermolytic ichthyosis Onychomatricoma Lelis syndrome Focal dermal hypoplasia Disseminated superficial actinic porokeratosis Uncombable hair syndrome Diffuse lymphatic malformation Genetic photodermatosis Erythromelalgia Disease with punctate palmoplantar keratoderma as a major feature Lipedema Steatocystoma multiplex-natal teeth syndrome Localized dystrophic epidermolysis bullosa, acral form Harlequin ichthyosis Ehlers-Danlos syndrome Scalp defects-postaxial polydactyly syndrome Familial multiple trichoepithelioma Gorlin-Chaudhry-Moss syndrome Hermansky-Pudlak syndrome Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome Xeroderma pigmentosum variant Multiple benign circumferential skin creases on limbs Alopecia-contractures-dwarfism-intellectual disability syndrome Primary cutaneous T-cell lymphoma Oculocutaneous albinism type 2 Osteopathia striata-pigmentary dermopathy-white forelock syndrome Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies Alopecia antibody deficiency Recessive X-linked ichthyosis Oculocutaneous albinism type 1A Hidrotic ectodermal dysplasia Nevus of Ota Porokeratosis of Mibelli Rothmund-Thomson syndrome type 1 Focal facial dermal dysplasia type II Alopecia-epilepsy-pyorrhea-intellectual disability syndrome Oculocutaneous albinism type 4 CLOVES syndrome Cockayne syndrome Familial normophosphatemic tumoral calcinosis Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome Oculocutaneous albinism type 3 Generalized basaloid follicular hamartoma syndrome Incontinentia pigmenti Oculocutaneous albinism Oculocutaneous albinism type 1B Porokeratosis plantaris palmaris et disseminata Severe achondroplasia-developmental delay-acanthosis nigricans syndrome Autosomal dominant cutis laxa Localized dystrophic epidermolysis bullosa, nails only Autosomal dominant palmoplantar keratoderma and congenital alopecia Skin fragility-woolly hair-palmoplantar keratoderma syndrome Cutis marmorata telangiectatica congenita Epidermolysis bullosa simplex with circinate migratory erythema Porphyria Oculocutaneous albinism type 5 Juvenile xanthogranuloma Corneodermatoosseous syndrome Autosomal recessive cutis laxa type 2 Hutchinson-Gilford progeria syndrome Focal facial dermal dysplasia type IV Autosomal recessive cutis laxa type 1 Alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome Hermansky-Pudlak syndrome due to BLOC-2 deficiency Hypohidrotic ectodermal dysplasia Congenital smooth muscle hamartoma Farber disease RIN2 syndrome Rothmund-Thomson syndrome type 2 Occipital horn syndrome Trichorhinophalangeal syndrome type 1 Proteus syndrome Hallermann-Streiff syndrome Brittle cornea syndrome Dahlberg-Borer-Newcomer syndrome Nevus of Ito Erythrokeratoderma variabilis progressiva Epidermolysis bullosa simplex with pyloric atresia Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering Autosomal dominant disease associated with punctate palmoplantar keratoderma as a major feature Isolated congenital digital clubbing CHIME syndrome Cowden syndrome Hypohidrotic ectodermal dysplasia with immunodeficiency Familial multiple fibrofolliculoma Autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature ALDH18A1-related De Barsy syndrome Crandall syndrome Toriello-Lacassie-Droste syndrome Cronkhite-Canada syndrome Classical-like Ehlers-Danlos syndrome type 1 Lethal acantholytic erosive disorder Familial progressive hyper- and hypopigmentation Odonto-tricho-ungual-digito-palmar syndrome Cleft lip/palate-ectodermal dysplasia syndrome Leukoencephalopathy-palmoplantar keratoderma syndrome Striate palmoplantar keratoderma KID syndrome Pachydermoperiostosis Leukonychia totalis Keratolytic winter erythema Congenital generalized hypertrichosis, Ambras type Arterial tortuosity syndrome Choroidal atrophy-alopecia syndrome Pure hair and nail ectodermal dysplasia Non-hereditary congenital primary lymphedema Schöpf-Schulz-Passarge syndrome Hartnup disease Ectodermal dysplasia with natal teeth, Turnpenny type Frontonasal dysplasia-alopecia-genital anomalies syndrome Oculocutaneous albinism type 6 Vascular-like classical Ehlers-Danlos syndrome B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome CEDNIK syndrome X-linked reticulate pigmentary disorder Milroy disease Curly hair-acral keratoderma-caries syndrome Limb-mammary syndrome Hereditary acrokeratotic poikiloderma of Kindler-Weary Familial melanoma Cutis laxa Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Hypotrichosis with juvenile macular degeneration UV-sensitive syndrome Epidermal nevus syndrome Amelo-onycho-hypohidrotic syndrome Hermansky-Pudlak syndrome due to BLOC-1 deficiency X-linked Ehlers-Danlos syndrome Atrichia with papular lesions Naegeli-Franceschetti-Jadassohn syndrome Familial cylindromatosis Diffuse cutaneous mastocytosis Ehlers-Danlos syndrome, fibronectinemic type Mal de Meleda Waardenburg syndrome type 1 Palmoplantar keratoderma, Nagashima type Pseudoxanthoma elasticum Cutaneous mastocytoma Waardenburg syndrome type 2 Deaf blind hypopigmentation syndrome, Yemenite type Oley syndrome Pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome Encephalocraniocutaneous lipomatosis Trichodental syndrome Waardenburg syndrome type 3 Hypotrichosis simplex of the scalp Tricho-dento-osseous syndrome Buschke-Ollendorff syndrome Autosomal dominant diffuse mutilating palmoplantar keratoderma Maculopapular cutaneous mastocytosis Familial multiple nevi flammei Multiple symmetric lipomatosis Trichodermodysplasia-dental alterations syndrome Cardiac-valvular Ehlers-Danlos syndrome Follicular atrophoderma-basal cell carcinoma Large congenital melanocytic nevus Tricho-oculo-dermo-vertebral syndrome Darier disease Trichoodontoonychial dysplasia Hypopigmentation-punctate palmoplantar keratoderma syndrome Hereditary sclerosing poikiloderma, Weary type Proliferating trichilemmal cyst Cerebellar ataxia-ectodermal dysplasia syndrome Craniofaciofrontodigital syndrome Deafness-enamel hypoplasia-nail defects syndrome Congenital reticular ichthyosiform erythroderma Hemihyperplasia-multiple lipomatosis syndrome Werner syndrome Ehlers-Danlos/osteogenesis imperfecta syndrome Familial keratoacanthoma Parana hard skin syndrome Hermansky-Pudlak syndrome type 8 Dermatomyositis Trichothiodystrophy Full schwannomatosis Hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome Cutaneous mastocytosis Transgrediens et progrediens palmoplantar keratoderma Verrucous nevus Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome Carvajal syndrome Inflammatory linear verrucous epidermal nevus Blepharo-cheilo-odontic syndrome Laryngo-onycho-cutaneous syndrome Netherton syndrome Musculocontractural Ehlers-Danlos syndrome Trichomegaly-retina pigmentary degeneration-dwarfism syndrome Acanthokeratolytic verrucous nevus Fanconi anemia Ichthyosis follicularis-alopecia-photophobia syndrome Trichodysplasia-xeroderma syndrome Erythropoietic uroporphyria associated with myeloid malignancy Autosomal dominant trichoodontoonychodysplasia-syndactyly Keratosis pilaris atrophicans Generalized pustular psoriasis Neurofibromatosis type 1 Full NF2-related schwannomatosis PASH syndrome Poikiloderma with neutropenia Mastocytosis Xeroderma pigmentosum Porphyria variegata Epidermolysis bullosa simplex superficialis Autosomal recessive nail dysplasia Trichorhinophalangeal syndrome type 2 Autosomal recessive generalized epidermolysis bullosa simplex Leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome Acute hepatic porphyria Deafness-onychodystrophy syndrome Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome Hereditary bullous dystrophy, macular type Centripetalis recessive dystrophic epidermolysis bullosa Progeria-short stature-pigmented nevi syndrome Rare systemic or rheumatologic disease Junctional epidermolysis bullosa, non-Herlitz type Graham Little-Piccardi-Lassueur syndrome Atypical Werner syndrome Hepatoerythropoietic porphyria Bullous diffuse cutaneous mastocytosis Rare lymphatic malformation Griscelli syndrome type 2 Telangiectasia macularis eruptiva perstans Dystrophic epidermolysis bullosa pruriginosa Chronic hepatic porphyria Hermansky-Pudlak syndrome due to AP-3 deficiency Griscelli syndrome type 1 Pemphigus vegetans Autosomal recessive generalized dystrophic epidermolysis bullosa, intermediate form De Barsy syndrome Familial anetoderma Dubowitz syndrome Progeroid syndrome, Petty type Conductive deafness-ptosis-skeletal anomalies syndrome Maffucci syndrome Griscelli syndrome type 3 Familial primary localized cutaneous amyloidosis Ataxia-telangiectasia Anonychia-onychodystrophy syndrome Systemic mastocytosis with associated hematologic neoplasm Diffuse palmoplantar keratoderma with painful fissures Pemphigus foliaceus Spät-einsetzende lokalisierte junktionale Epidermolysis bullosa-Intelligenzminderung-Syndrom Mastzellsarkom Mikrophthalmie-lineares Hautdefekt-Syndrom Autosomal-rezessive Krankheit mit diffuser Palmoplantarkeratose als Hauptmerkmal Pemphigus erythematosus Hermansky-Pudlak-Syndrom Typ 9 COFS-Syndrom Indolente systemische Mastozytose Mastzell-Leukämie Hypotrichose-Schwerhörigkeit-Syndrom Keratosis linearis-Ichthyosis congenita-sklerosierendes Keratoderm-Syndrom Ehlers-Danlos-Syndrom, parodontaler Typ Phakomatosis cesiomarmorata Mastzell-Leukämie, agressive PENS-Syndrom Haut, granulomatöse schlaffe Schwere Dermatitis-multiple Allergien-metabolischer Verlust-Syndrom Blue rubber bleb-Naevus Kollagenom, familiäres kutanes Mastozytom, extrakutanes Gorlin-Syndrom Phakomatosis cesioflammea Neonatale Haut- und Darmerkrankung, entzündliche Dyschromatosis universalis hereditaria Kutane Mastozytose, diffuse pseudoxanthomatöse Proteus-ähnliches Syndrom Naevus comedonicus-Syndrom Zahn-Nagel-Syndrom Typ Fried Hypotrichosis-Osteolysis-Periodontitis-Palmoplantarkeratose-Syndrom Stiff-skin-Syndrom Hygrom, zystisches Pyramidale Molare-Oberlippenanomalie-Syndrom Becker Naevus-Syndrom Phakomatosis spilorosea Knuckle-Pads-Leukonychie-sensorineurale Schwerhörigkeit-palmoplantare Hyperkeratose-Syndrom Griscelli-Syndrom Hyperkeratose-Hyperpigmentierung-Syndrom Hypohidrotische ektodermale Dysplasie-Hypothyreose-Ziliendyskinesie-Syndrom Bannayan-Riley-Ruvalcaba-Syndrom Ichthyose Pellagra-ähnliches-Syndrom Rombo-Syndrom Talgdrüsentumor, palpebraler Lymphatische Malformation, mikrozystische Noonan-ähnliches Syndrom mit losem Anagenhaar Ektodermale Dysplasie-sensorineurale Schwerhörigkeit-Syndrom Lymphatische Malformation, makrozystische Ichthyose-Syndrom, autosomales Terminale Knochendysplasie - Pigmentstörungen Pili gemini SAPHO-Syndrom Huriez-Syndrom Tietz-Syndrom Dysplasie, ektodermale hypohidrotische, autosomal-rezessive Anonychie mit umschriebener Pigmentierung Ichthyose-Syndrom, X-chromosomales Kardio-fazio-kutanes Syndrom Pemphigus superficial Gelenkhypermobilitäts-Syndrom, familiäres Bazex-Dupré-Christol-Syndrom Epidermolysis bullosa, dystrophe, generalisierte, autosomal-dominante Epidermolysis bullosa, erworbene PAPA-Syndrom Pemphigus, benigner chronischer familiärer Hypertrichose, ventrale zervikale, isolierte Schleimhautpemphigoid Tumorale Kalzinose, familiäre Hereditäre Leiomyomatose mit Nierenzellkrebs Fokale Palmoplantarkeratose mit Hyperkeratose an den Gelenken IgA-Dermatose, lineare Brooke-Spiegler-Syndrom Palmoplantarkeratose, hereditäre Ichthyose-Syndrom, autosmales, mit prominenten Haaranomalitäten Hautkrankheit, genetische, unklassifizierte Ankyloblepharon-ektodermale Defekte-Lippen-Kiefer-Gaumenspalte-Syndrom Lippen-Kiefer-Gaumen-Spalte-ektodermale Dysplasie-Syndrom Hypertrichose, generalisierte kongenitale, X-chromosomale Schinzel-Giedion-Syndrom Gingiva-Fibromatose-Hypertrichose-Syndrom Maculae, hypopigmentierte und hyperpigmentierte, hereditäre kongenitale Pemphigus herpetiformis Schwerhörigkeit-Onychodystrophie-Syndrom, autosomal-dominantes Naxos-Krankheit Epidermolysis bullosa, hereditäre Dysplasie, okulo-dento-digitale Fibromatose, hyaline juvenile Epidermale Krankheit, genetisch bedingte Cutis laxa, autosomal-rezessive, Typ 2A T-Zell-Lymphom, primär kutanes, klein/mittelgroßzelliges pleomorphes, CD4-+ Lipomatose, mesosomatische, Typ Roch-Leri Kontrakturen-ektodermale Dysplasie-Lippen-Kiefer-Gaumenspalte-Syndrom Alopezie Ichthyose, hereditäre, nicht-syndromale Form Palmoplantarkeratose, punktierte, Typ I Epidermolysis bullosa simplex mit Muskeldystrophie Legius-Syndrom Fibrosarkom Chondrodysplasia punctata, X-chromosomal-dominante Lipoidproteinose Undifferenzierte Kollagenosen DOORS-Syndrom Birt-Hogg-Dubé-Syndrom Haarschaftanomalie, isolierte Okulo-osteo-kutanes Syndrom Kyphoskoliotisches Ehlers-Danlos-Syndrom durch FKBP22-Defizienz Systemische Sklerose, diffuse kutane Ledderhose-Krankheit Erythema palmare hereditarium Ichthyosis hystrix Curth-Macklin Alopezie-Intelligenzminderung-Syndrom Seltene Krankheit mit Hypertrichose Pterygium-Syndrom, antekubitales Björnstad-Syndrom Cooks-Syndrom EEC-Syndrom Pustulosis Palmaris et Plantaris Dermotrichales Syndrom Ichthyose, hereditäre, syndromale Form Palmoplantarkeratose, punktierte, Typ 2 PYCR1-assoziiertes De Barsy-Syndrom H-Syndrom EEM syndrome Chilblain lupus Isolated nail anomaly Superficial fibromatosis Syndromic hair shaft abnormality Autosomal recessive cutis laxa type 2B Bloom syndrome Ichthyosis hystrix gravior Primary cutis verticis gyrata Rare cutaneous lupus erythematosus Arthrochalasia Ehlers-Danlos syndrome Autosomal recessive multiple pterygium syndrome Familial cold urticaria Porphyria cutanea tarda Hypertrophic or verrucous lupus erythematosus Pachyonychia congenita Autosomal recessive congenital ichthyosis Oculotrichodysplasia Pemphigoid gestationis Scalp-ear-nipple syndrome Acrodermatitis continua of Hallopeau Discoid lupus erythematosus Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency Isolated diffuse palmoplantar keratoderma Inherited ichthyosis Oculocerebral hypopigmentation syndrome, Cross type Punctate palmoplantar keratoderma Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome Syndromic nail anomaly Dermatosparaxis Ehlers-Danlos syndrome Syndromic recessive X-linked ichthyosis Atrophoderma vermiculata Ectodermal dysplasia syndrome Diffuse palmoplantar keratoderma Lupus erythematosus tumidus Limited cutaneous systemic sclerosis Vici syndrome Odonto-onycho-dermal dysplasia CLAPO syndrome Genetic acrokeratoderma Subacute cutaneous lupus erythematosus Lymphedema-distichiasis syndrome Calcifying aponeurotic fibroma Odonto-onycho dysplasia-alopecia syndrome Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma Genetic erythrokeratoderma Lupus erythematosus panniculitis Familial generalized lentiginosis Carney complex Porphyria due to ALA dehydratase deficiency Odontotrichomelic syndrome Adult T-cell leukemia/lymphoma Primary cutaneous CD30+ T-cell lymphoproliferative disease