Category:Genodermatoses
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Genodermatoses are inherited genetic skin conditions often grouped into three categories—chromosomal, single gene, and polygenetic.
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Pages in category "Genodermatoses"
The following 200 pages are in this category, out of 237 total.
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- Acne vermoulanti
- Acral peeling skin syndrome
- Acrocephalosyndactylia
- Acrodermatitis
- Acrodermatitis enteropathica
- Acrogeria
- Adams–Oliver syndrome
- Adducted thumbs syndrome
- Adult progeria
- Albright's hereditary osteodystrophy
- Alpha-N-acetylgalactosaminidase deficiency
- Angelman syndrome
- Anhidrotic ectodermal dysplasia
- Ankyloblepharon filiforme adnatum–ectodermal dysplasia–cleft palate syndrome
- Ankyloblepharon–ectodermal defects–cleft lip and palate syndrome
- Ankyloblepharon–ectodermal dysplasia–clefting syndrome
- Apert syndrome
- Arthrogryposis–renal dysfunction–cholestasis syndrome
- Ataxia telangiectasia
- Atrophoderma reticulatum
- Atrophodermia reticulata symmetrica faciei
- Atrophodermia ulerythematosa
- Atrophodermia vermiculata
- Autosomal recessive chondrodysplasia punctata type 1
B
C
- CAP syndrome
- Cardiofaciocutaneous syndrome
- Cartilage–hair hypoplasia
- CEDNIK syndrome
- Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome
- Childhood tumor syndrome
- Chondrodysplasia punctata
- Christ–Siemens–Touraine syndrome
- Clouston syndrome
- Cockayne syndrome
- Collodion baby
- Colobomas of the eye–heart defects–ichthyosiform dermatosis–mental retardation–ear defects syndrome
- Congenital absence of skin
- Congenital poikiloderma with blisters and keratoses
- Congenital poikiloderma with bullae and progressive cutaneous atrophy
- Congenital scars
- Conradi–Hünermann syndrome
- Costello syndrome
- Craniosynostosis–anal anomalies–porokeratosis syndrome
- Cronkhite–Canada syndrome
- Crouzon syndrome
- Cutis aplasia
D
- Darier's disease
- Delleman–Oorthuys syndrome
- Dermatopathia pigmentosa reticularis
- Diffuse non-epidermolytic palmoplantar keratoderma with woolly hair and cardiomyopathy
- Dolichol kinase deficiency
- Dyschromatosis universalis hereditaria
- Dyskeratosis congenita
- Dyskeratosis follicularis
- Dystrophic epidermolysis bullosa
E
F
H
- Haber syndrome
- Hailey–Hailey disease
- Haim–Munk syndrome
- Hallopeau–Siemens disease
- Hallopeau–Siemens variant of epidermolysis bullosa
- Harlequin baby
- Harlequin ichthyosis
- Harlequin-type ichthyosis
- Hay–Wells syndrome
- Hereditary acrokeratotic poikiloderma
- Hereditary painful callosities
- Heterochromia iridum
- Hidrotic ectodermal dysplasia
- Holocarboxylase synthetase deficiency
- Honeycomb atrophy
- Hutchinson–Gilford syndrome
- Hypohidrotic ectodermal dysplasia
I
- Ichthyosis
- Ichthyosis bullosa of Siemens
- Ichthyosis hystrix of Curth–Macklin
- Ichthyosis prematurity syndrome
- Ichthyosis vulgaris
- Ichthyosis with confetti
- Ichthyosis–brittle hair–impaired intelligence–decreased fertility–short stature syndrome
- Immune dysfunction–polyendocrinopathy–enteropathy–X-linked syndrome
- Infantile Refsum disease
J
K
- Kabuki makeup syndrome
- Kabuki syndrome
- Keratolytic winter erythema
- Keratosis follicularis
- Keratosis follicularis spinulosa decalvans
- Keratosis linearis with ichthyosis congenital and sclerosing keratoderma syndrome
- Keratosis pilaris
- Keratosis pilaris atrophicans faciei
- KID syndrome
- Kindler syndrome
- KLICK syndrome
- Klippel–Feil syndrome
L
M
N
- Naegeli–Franceschetti–Jadassohn syndrome
- Naxos disease
- Naxos syndrome
- Neonatal ichthyosis–sclerosing cholangitis syndrome
- Neurofibromatosis
- Neurofibromatosis type 1
- Neutral lipid storage disease
- Niikawa–Kuroki syndrome
- Noonan syndrome
- Noonan Syndrome with Multiple Lentigines
- Noonan syndrome with multiple lentigines
- Nummular epidermolytic palmoplantar keratoderma
O
P
- Pachyderma
- Pachyonychia congenita
- Palmoplantar keratoderma of the Norrbotten type
- Palmoplantar keratoderma with periodontitis
- Palmoplantar keratoderma with periodontitis and arachnodactyly and acro-osteolysis
- Palmoplantar keratoderma with scleroatrophy
- Papillon–Lefèvre syndrome
- Pfeiffer syndrome
- Photosensitivity–ichthyosis–brittle sulfur-deficient hair–impaired intelligence–decreased fertility–short stature syndrome
- Phytanic acid storage disease
- Plakophilin 1 deficiency
- POEMS syndrome
- Polyneuropathy–organomegaly–endocrinopathy–monoclonal gammopathy–skin changes syndrome
- Polyostotic fibrous dysplasia
- Popliteal pterygium syndrome
- Porokeratosis
- Porokeratosis of Mibelli
- Prader–Willi syndrome
- Primary hypertrophic osteoathropathy
- Progeria
- Progeria syndrome
- Progressive cribriform and zosteriform hyperpigmentation
- Progressive osseous heteroplasia
- Proteus syndrome
- Proteus-like syndrome
