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Hypotrichosis-deafness syndrome
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Porokeratotic eccrine ostial and dermal duct nevus
1 associated gene
No signs/symptoms info
Hypotrichosis-deafness syndrome
Porokeratotic eccrine ostial and dermal duct nevus

GJB2
(UniProt - OMIM)
 GJB2
(UniProt - OMIM)

COMMON
GENES 		GJB2


Citations in the biomedical literature:


Hypotrichosis-deafness syndrome
GJB2
Porokeratotic eccrine ostial and dermal duct nevus



Hypotrichosis-deafness syndrome
Porokeratotic eccrine ostial and dermal duct nevus

Synonym(s):
(no synonyms)

Synonym(s):
- Comedo nevus of the palm
- Porokeratotic eccrine nevus
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare otorhinolaryngologic disease
- Rare skin disease
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.