hearing loss, autosomal dominant 76
MONDO:0032917Mondo
Findings
No curated finding names hearing loss, autosomal dominant 76 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Infantile onset
HPO, annotations 2026-09-02
Features
4 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Sensorineural hearing impairmentHPOHP:0000407
- 4 of 4 reported patients
- Abnormal vestibular functionHPOHP:0001751
- 0 of 4 reported patients
- Motor delayHPOHP:0001270
- 0 of 4 reported patients
- Positive Romberg signHPOHP:0002403
- 0 of 4 reported patients
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.
- PLS1HGNC:9090
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2022
- Strong · PanelApp Australia · Autosomal dominant · 2025
- Moderate · Ambry Genetics · Autosomal dominant · 2023