autosomal recessive nonsyndromic hearing loss 13
MONDO:0011286Mondo
Findings
No curated finding names autosomal recessive nonsyndromic hearing loss 13 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An autosomal recessive nonsyndromic deafness that has material basis in variation in the chromosome region 7q34-q36.
Definition from the Mondo Disease Ontology (MONDO:0011286), read 2026-09-29. CC BY 4.0.
Features
2 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.
- Hearing impairmentHPOHP:0000365
- Sensorineural hearing impairmentHPOHP:0000407
Where it sits
- A kind of