autosomal dominant nonsyndromic hearing loss 49
MONDO:0012023Mondo
Findings
No curated finding names autosomal dominant nonsyndromic hearing loss 49 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An autosomal dominant nonsyndromic deafness that is characterized by moderate loss for low and mid frequencies and mild loss for high frequencies and has material basis in variation in the chromosome region 1q21-q23.
Definition from the Mondo Disease Ontology (MONDO:0012023), read 2026-09-29. CC BY 4.0.