autosomal recessive nonsyndromic hearing loss 2
MONDO:0010807Mondo
Findings
No curated finding names autosomal recessive nonsyndromic hearing loss 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO7A gene.
Definition from the Mondo Disease Ontology (MONDO:0010807), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- MYO7AHGNC:7606
- Definitive · G2P · Autosomal recessive · 2025
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Moderate · Ambry Genetics · Autosomal recessive · 2022
Where it sits
- A kind of