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Porokeratotic eccrine ostial and dermal duct nevus
1 associated gene
14 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
KID syndrome
Hypotrichosis-deafness syndrome
Keratoderma hereditarium mutilans
Knuckle pads-leuconychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome
Palmoplantar keratoderma-deafness syndrome
Berardinelli-Seip congenital lipodystrophy
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
X-linked Charcot-Marie-Tooth disease type 1
X-linked progressive cerebellar ataxia
Hidrotic ectodermal dysplasia
Synonym(s):
- Comedo nevus of the palm
- Porokeratotic eccrine nevus
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
GJB2 P29033121011
No signs/symptoms info available.