auditory neuropathy-optic atrophy syndrome
MONDO:0060582Mondo
Findings
No curated finding names auditory neuropathy-optic atrophy syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Juvenile onset · Childhood onset
HPO, annotations 2026-09-02
Features
5 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
- 8 of 8 reported patients
- Optic atrophyHPOHP:0000648
- 8 of 8 reported patients
- Visual impairmentHPOHP:0000505
- 8 of 8 reported patients
- NystagmusHPOHP:0000639
- 1 of 8 reported patients
- Rod-cone dystrophyHPOHP:0000510
- 1 of 8 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.
- FDXRHGNC:3642
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2023
- Strong · G2P · Autosomal recessive · 2025
- Supportive · Orphanet · Autosomal recessive · 2021
Where it sits
Other names
3 names
Resolves to: auditory neuropathy-optic atrophy syndrome
- Also called
- ANOAauditory neuropathy and optic atrophymultiple mitochondrial dysfunctions syndrome 9A