Disease #05363 (ANOA;MMDS9A (neuropathy, auditory, and optic atrophy), OMIM:617717)
| Official abbreviation |
ANOA;MMDS9A |
| Name |
neuropathy, auditory, and optic atrophy |
| OMIM ID |
617717 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
FDXR |
| Associated tissues |
- |
| Disease features |
autosomal recessive |
| Remarks |
- |
| Date created |
2017-12-29 14:15:12 +01:00 (CET) |
| Date last edited |
2024-11-25 10:17:09 +01:00 (CET) |
Individuals
|