autosomal dominant nonsyndromic hearing loss 43
MONDO:0012030Mondo
Findings
No curated finding names autosomal dominant nonsyndromic hearing loss 43 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An autosomal dominant nonsyndromic deafness that has material basis in variation in the chromosome region 2p12.
Definition from the Mondo Disease Ontology (MONDO:0012030), read 2026-09-29. CC BY 4.0.