autosomal recessive nonsyndromic hearing loss 39
MONDO:0012003Mondo
Findings
No curated finding names autosomal recessive nonsyndromic hearing loss 39 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An autosomal recessive disorder caused by mutations in the HGF gene, encoding hepatocyte growth factor receptor. It is characterized by profound deafness.
Definition from the Mondo Disease Ontology (MONDO:0012003), 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.
- HGFHGNC:4893
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2018
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2018
- Limited · G2P · Autosomal recessive · 2025
Where it sits
- A kind of