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Hay-wells Syndrome
Hay-Wells syndrome
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Rare diseases
(17)
Lelis syndrome
Familial cutaneous papillomatosis
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Kindler syndrome
Bloom syndrome
Naegeli syndrome
Harlequin type ichthyosis
Netherton syndrome
Epidermolysis bullosa simplex
Epidermolytic hyperkeratosis
Hermansky-Pudlak syndrome
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Syndromes
(10)
Eec syndrome
Alport syndrome
Syndrome
Lelis syndrome
Eem syndrome
Eem syndrome
Zunich Kaye syndrome
Bloom syndrome
Naegeli syndrome
Netherton syndrome
Hermansky-Pudlak syndrome
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Genetic disorders
(15)
DNA repair-deficiency disorder
Hereditary motor sensory neuropathy
Lelis syndrome
Familial cutaneous papillomatosis
Eem syndrome
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Ichthyosis lamellaris
Congenital ichthyosiform erythroderma
Dermatopathia pigmentosa reticularis
Kindler syndrome
Bloom syndrome
Netherton syndrome
Alport syndrome
Hermansky-Pudlak syndrome
more...
Genodermatoses
(157)
Ectodermal dysplasia
Epidermolysis bullosa dystrophica
Focal dermal hypoplasia
Hypohidrotic ectodermal dysplasia
Rapp-hodgkin syndrome
Rapp-hodgkin syndrome
X-linked ichthyosis
18q deletion syndrome
Acrocephal- osyndactylia
Acrodermatitis enteropathica
Acrokeratosis verruciformis
Adams–Oliver syndrome
Adducted thumbs syndrome
Albright's hereditary osteodystrophy
Apert syndrome
Aplasia cutis congenita
Arrhythmogenic right ventricular dysplasia
Ataxia telangiectasia
Atrichia with papular lesions
Atrophodermia vermiculata
Autoimmune polyendocr- inopathy–candidiasis–ectodermal dystrophy syndrome
BIDS syndrome
Bart syndrome
Bloom syndrome
CHILD syndrome
Cardiofaci- ocutaneous syndrome
Cartilage–hair hypoplasia
Carvajal syndrome
Chondrodysplasia punctata
Cicatricial junctional epidermolysis bullosa
Clouston's hidrotic ectodermal dysplasia
Cockayne syndrome
Congenital ichthyosiform erythroderma
Conradi–Hünermann syndrome
Costello syndrome
Cronkhite-Canada syndrome
Crouzon syndrome
Cutis verticis gyrata
Darier's disease
Dermatopathia pigmentosa reticularis
Disseminated superficial actinic porokeratosis
Disseminated superficial porokeratosis
Dominant dystrophic epidermolysis bullosa
Dyschromatosis universalis hereditaria
Dyskeratosis congenita
Ectodermal dysplasia with corkscrew hairs
Eec syndrome
Epidermolysis bullosa
Epidermolysis bullosa herpetiformis
Epidermolysis bullosa simplex
Epidermolysis bullosa simplex of Ogna
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolytic hyperkeratosis
Erythrokeratodermia variabilis
Familial cutaneous papillomatosis
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
Follicular atrophoderma
Franceschetti–Klein syndrome
Freeman-Sheldon syndrome
Generalized atrophic benign epidermolysis bullosa
Generalized epidermolysis bullosa simplex
Generalized trichoepithelioma
Hailey-Hailey disease
Hallermann-Streiff syndrome
Harlequin type ichthyosis
Hereditary sclerosing poikiloderma
IBIDS syndrome
IFAP syndrome
Ichthyosis
Ichthyosis bullosa of Siemens
Ichthyosis hystrix
Ichthyosis lamellaris
Ichthyosis linearis circumflexa
Ichthyosis vulgaris
IgA pemphigus
Incontinentia pigmenti
Incontinentia pigmenti achromians
Junctional epidermolysis bullosa (medicine)
Junctional epidermolysis bullosa gravis
Keratitisâ- €“ichthyosis–deafness syndrome
Keratolytic winter erythema
Keratosis follicularis spinulosa decalvans
Keratosis pilaris
Keratosis pilaris atrophicans faciei
Kindler syndrome
Klinefelter's syndrome
Klippel–Feil syndrome
LEOPARD syndrome
Lelis syndrome
Lentiginosis
Lenz–Majewski syndrome
Linear Darier disease
Linear and whorled nevoid hypermelanosis
Linear porokeratosis
Localized epidermolysis bullosa simplex
Mandibuloacral dysplasia
Marinesco–Sjögren syndrome
McCusick syndrome
Meleda Disease
Mitis junctional epidermolysis bullosa
Multiple sulfatase deficiency
Naegeli syndrome
Netherton syndrome
Neurofibromatosis
Neurofibromatosis type 3
Neurofibromatosis type 4
Neurofibromatosis type I
Neutral lipid storage disease
Noonan syndrome
Odonto–T- richo–Ungual–Digital–Palmar syndrome
PIBI(D)S syndrome
POEMS syndrome
Pachydermo- periostosis
Pachyonychia congenita
Pachyonychia congenita type I
Pachyonychia congenita type II
Papillon–Lefèvre syndrome
Peeling skin syndrome
Pfeiffer syndrome
Pityriasis rotunda
Plaque-type porokeratosis
Polyostotic fibrous dysplasia
Popliteal pterygium syndrome
Porokeratosis
Porokeratosis palmaris et plantaris disseminata
Progeria
Progressive symmetric erythrokeratodermia
Proteus syndrome
Punctate porokeratosis
Recessive dystrophic epidermolysis bullosa
Refsum's disease
Relapsing linear acantholytic dermatosis
Restrictive dermopathy
Rhizomelic chondrodysplasia punctata
Rombo syndrome
Rothmund–Thomson syndrome
Scleroatrophic syndrome of Huriez
Sjögren–Larsson syndrome
Tooth and nail syndrome
Transient bullous dermolysis of the newborn
Treacher Collins syndrome
Tricho–r- hino–phalangeal syndrome
Tuberous sclerosis
Turner syndrome
Ulerythema
Ulnar–mammary syndrome
Von Hippel – Lindau disease
Watson syndrome
Werner syndrome
Westerhof syndrome
Wilson–Turner syndrome
Wolf–Hirschhorn syndrome
X-linked recessive chondrodysplasia punctata
XXYY syndrome
Xeroderma pigmentosum
Zimmermann–Laband syndrome
Zunich Kaye syndrome
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Diseases and disorders
(30)
Ankyloblepharon filiforme adnatum cleft palate
Myhre syndrome
Adult syndrome
Hypohidrosis
Supernumerary nipples
Supernumerary nipples
Cleft lip
Hemangioma
Acanthosis nigricans
Skin cancer
Hypospadias
Syndromes
Eem syndrome
Gerodermia osteodysplastica
Zunich Kaye syndrome
Meleda Disease
Ichthyosis lamellaris
Dermatopathia pigmentosa reticularis
Epidermolysis bullosa dystrophica
Ectodermal dysplasia
Bloom syndrome
Naegeli syndrome
Harlequin type ichthyosis
Hypohidrotic ectodermal dysplasia
Focal dermal hypoplasia
Hereditary motor sensory neuropathy
Netherton syndrome
Epidermolysis bullosa simplex
X-linked ichthyosis
Alport syndrome
Hermansky-Pudlak syndrome
more...
Congenital disorders
Congenital malformations
Holoprosencephaly
Cleft lip
Hypospadias
Cutaneous conditions
Papulosquamous hyperkeratotic skin diseases
Acral Acanthotic Anomaly
Acne aestivalis
See also
(20)
Nevus flammeus nuchae
Autosomal dominant
Autosomal recessive
TP73L
Integument
Integument
Subcutaneous tissue
Birthmarks
Ectodermal
Acrodermatitis Chronica Atrophicans
Places
Clefting
Hypodontia
Acantholysis
Cadherin
Epidermis (skin)
Craniofacial
OMIM
The Skin
Mutations
PMID
more...
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