GJB2-related disorder

Findings

No curated finding names GJB2-related disorder yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

Where it sits

A kind of

• hereditary disease

Narrower terms (7)

• autosomal dominant keratitis-ichthyosis-hearing loss syndrome
• autosomal dominant nonsyndromic hearing loss 3A
• autosomal recessive nonsyndromic hearing loss 1A
• Bart-Pumphrey syndrome
• ichthyosis, hystrix-like, with hearing loss
• keratoderma hereditarium mutilans
• palmoplantar keratoderma-deafness syndrome

Resolves to: GJB2-related disorder

Also called

GJB2-related conditions