Category:Genodermatoses
From HandWiki
Here is a list of articles in the category Genodermatoses of the Medicine portal.
 | Pages in this category should be moved to subcategories where applicable. This category may require frequent maintenance to avoid becoming too large. It should directly contain very few, if any, pages and should mainly contain subcategories. |
Genodermatoses are inherited genetic skin conditions often grouped into three categories—chromosomal, single gene, and polygenetic.
Pages in category "Genodermatoses"
The following 200 pages are in this category, out of 418 total.
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- Medicine:Ichthyosis hystrix of Curth–Macklin
- Medicine:Ichthyosis linearis circumflexa
- Medicine:Ichthyosis prematurity syndrome
- Medicine:Ichthyosis simplex
- Medicine:Ichthyosis vulgaris
- Medicine:Ichthyosis with confetti
- Medicine:Ichthyosis–brittle hair–impaired intelligence–decreased fertility–short stature syndrome
- Medicine:Idiopathic deciduous skin
- Medicine:Idiopathic hypertrophic osteoathorpathy
- Medicine:Immune dysfunction–polyendocrinopathy–enteropathy–X-linked syndrome
- Medicine:Incontinentia pigmenti achromians
- Medicine:Infantile Refsum disease
J
K
- Medicine:Kabuki makeup syndrome
- Medicine:Kabuki syndrome
- Medicine:Kanzaki disease
- Medicine:Keratitis–ichthyosis–deafness syndrome
- Medicine:Keratolysis exfoliativa congenita
- Medicine:Keratolytic winter erythema
- Medicine:Keratosis follicularis
- Medicine:Keratosis follicularis spinulosa decalvans
- Medicine:Keratosis palmaris with drumstick fingers
- Medicine:Keratosis palmoplantaris nummularis
- Medicine:Keratosis pilaris
- Medicine:Keratosis pilaris atrophicans faciei
- Medicine:Keratosis pilaris rubra atrophicans faciei
- Medicine:KID syndrome
- Medicine:Kindler syndrome
- Medicine:KLICK syndrome
- Medicine:Klippel–Feil syndrome
- Medicine:Koebner variant of generalized epidermolysis bullosa simplex
L
- Medicine:Lamellar ichthyosis
- Medicine:Laryngo-onycho-cutaneous syndrome
- Medicine:Laryngo–onycho–cutaneous syndrome
- Medicine:Laryngoonychocutaneous syndrome
- Medicine:Legius syndrome
- Medicine:Lelis syndrome
- Medicine:Lentiginosis
- Medicine:Lentiginosis profusa syndrome
- Medicine:Lenz–Majewski syndrome
- Medicine:Leschke syndrome
- Medicine:Lethal acantholytic epidermolysis bullosa
- Medicine:Lethal junctional epidermolysis bullosa
- Medicine:Lhermitte–Duclos disease
- Medicine:Lichen pilare
- Medicine:Linear and whorled nevoid hypermelanosis
- Medicine:Linear Darier disease
- Medicine:Linear nevoid hyperpigmentation
- Medicine:Louis-Bar syndrome
- Medicine:Louis–Bar syndrome
M
- Medicine:Mandibuloacral dysplasia
- Medicine:Mandibulofacial dysostosis
- Medicine:Marinesco–Sjögren syndrome
- Medicine:McCune–Albright syndrome
- Medicine:McCusick syndrome
- Medicine:McKusick type metaphyseal chondrodysplasia
- Medicine:MELAS syndrome
- Medicine:Meleda disease
- Medicine:Mendes da Costa type erythrokeratodermia
- Medicine:Metageria
- Medicine:Microphthalmia–dermal aplasia–sclerocornea syndrome
- Medicine:MIDAS syndrome
- Medicine:Moynahan syndrome
- Medicine:Mucosulfatidosis
- Medicine:Multiple lentigines syndrome
- Medicine:Multiple pterygium syndrome
- Medicine:Multiple sulfatase deficiency
- Medicine:Mutilating palmoplantar keratoderma of the Gamborg–Nielsen type
N
- Medicine:Naegeli–Franceschetti–Jadassohn syndrome
- Medicine:Naxos disease
- Medicine:Naxos syndrome
- Medicine:Neonatal ichthyosis–sclerosing cholangitis syndrome
- Medicine:Netherton syndrome
- Medicine:Neurofibromatosis
- Medicine:Neurofibromatosis mixed type
- Medicine:Neurofibromatosis type 1
- Medicine:Neurofibromatosis type 1-like syndrome
- Medicine:Neurofibromatosis type 3
- Medicine:Neurofibromatosis type 4
- Medicine:Neurofibromatosis variant type
- Medicine:Neutral lipid storage disease
- Medicine:Niikawa–Kuroki syndrome
- Medicine:NISCH syndrome
- Medicine:Nonbullous congenital ichthyosiform erythroderma
- Medicine:Nonlethal junctional epidermolysis bullosa
- Medicine:Noonan syndrome
- Medicine:Noonan syndrome with multiple lentigines
- Medicine:Nummular epidermolytic palmoplantar keratoderma
O
P
- Medicine:Pachyderma
- Medicine:Pachydermoperiostosis
- Medicine:Pachyonychia congenita
- Medicine:Palmoplantar ectodermal dysplasia type VIII
- Medicine:Palmoplantar keratoderma and clubbing
- Medicine:Palmoplantar keratoderma of the Norrbotten type
- Medicine:Palmoplantar keratoderma with periodontitis
- Medicine:Palmoplantar keratoderma with scleroatrophy
- Medicine:Palmoplantar keratoderma with sclerodactyly
- Medicine:Papillon–Lefèvre syndrome
- Medicine:Papular atrichia
- Medicine:Peeling skin syndrome
- Medicine:Peroxisomal biogenesis disorder complementation group 11
- Medicine:Photosensitivity–ichthyosis–brittle sulfur-deficient hair–impaired intelligence–decreased fertility–short stature syndrome
- Medicine:Phytanic acid storage disease
- Medicine:Pityriasis circinata
- Medicine:Pityriasis rotunda
- Medicine:Plakophilin 1 deficiency
- Medicine:Plate-like osteoma cutis
- Medicine:POEMS syndrome
- Medicine:Poikiloderma congenitale
- Medicine:Polyneuropathy–organomegaly–endocrinopathy–monoclonal gammopathy–skin changes syndrome
- Medicine:Polyostotic fibrous dysplasia
- Medicine:Popliteal pterygium syndrome
- Medicine:Porokeratosis
- Medicine:Porokeratosis of Mibelli
- Medicine:Prader–Willi syndrome
- Medicine:Primary hypertrophic osteoathropathy
- Medicine:Progeria
- Medicine:Progeria syndrome
- Medicine:Progressive cardiomyopathic lentiginosis
- Medicine:Progressive cribriform and zosteriform hyperpigmentation
- Medicine:Progressive osseous heteroplasia
- Medicine:Progressive symmetric erythrokeratodermia
- Medicine:Proteus syndrome
- Medicine:Proteus-like syndrome
R
- Medicine:Rapp–Hodgkin ectodermal dysplasia syndrome
- Medicine:Rapp–Hodgkin syndrome
- Biology:RASopathy
- Medicine:Refsum disease
- Medicine:Relapsing linear acantholytic dermatosis
- Medicine:Restrictive dermopathy
- Medicine:Reticulate and zosteriform hyperpigmentation
- Medicine:Reticulate hyperpigmentation of Iijima, Naito and Uyeno
- Medicine:Rhizomelic chondrodysplasia punctata
- Medicine:Rombo syndrome
- Medicine:Rothmund–Thomson syndrome
S
- Medicine:Say syndrome
- Medicine:Scalp–ear–nipple syndrome
- Medicine:Schafer-Brunauer syndrome
- Medicine:Schindler disease
- Medicine:Scleroatrophic and keratotic dermatosis of the limbs
- Medicine:Sclerotylosis
- Medicine:Segmental neurofibromatosis
- Medicine:Senter syndrome
- Medicine:Siemens-1 syndrome
- Medicine:Silver–Russell syndrome
- Medicine:Sjögren–Larsson syndrome
- Medicine:Skin fragility syndrome
- Medicine:Smith–Lemli–Opitz syndrome
- Medicine:SNUB syndrome
- Medicine:Split hand–split foot–ectodermal dysplasia–cleft syndrome
- Medicine:Steroid sulfatase deficiency
- Medicine:Sturge–Weber syndrome
- Medicine:Sulfur-deficient brittle hair syndrome
- Medicine:Supernumerary nipples–uropathies–Becker's nevus syndrome
T
- Medicine:Tay's syndrome
- Medicine:Terminal osseous dysplasia with pigmentary defects
- Medicine:Tinea circinata
- Medicine:Tooth and nail syndrome
- Medicine:Touraine-Solente-Gole syndrome
- Medicine:Touraine–Solente–Gole syndrome
- Medicine:Townes–Brocks syndrome
- Medicine:Transient bullous dermolysis of the newborn
- Medicine:Treacher Collins syndrome
- Medicine:Treacher Collins–Franceschetti syndrome
- Medicine:Tricho–rhino–phalangeal syndrome
- Medicine:Tricho–rhino–phalangeal syndrome type 2
- Medicine:Trichothiodystrophy
- Medicine:Trichothiodystrophy with ichthyosis
- Medicine:Tuberous sclerosis
- Medicine:Turner syndrome
