autosomal dominant nonsyndromic hearing loss 7
MONDO:0011074Mondo
Findings
No curated finding names autosomal dominant nonsyndromic hearing loss 7 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 progressive high-tone hearing loss and has material basis in variation in the chromosome region 1q21-q23.
Definition from the Mondo Disease Ontology (MONDO:0011074), 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.
- LMX1AHGNC:6653
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022
- Strong · PanelApp Australia · Semidominant · 2025
- Limited · Ambry Genetics · Autosomal dominant · 2018
- Limited · Ambry Genetics · Autosomal dominant · 2025