Disease #05194 (OPA10 (atrophy, optic, type 10, with/without ataxia, mental retardation, and seizures (OPA-10)), OMIM:616732)
| Official abbreviation |
OPA10 |
| Name |
atrophy, optic, type 10, with/without ataxia, mental retardation, and seizures (OPA-10) |
| OMIM ID |
616732 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
RTN4IP1 |
| Associated tissues |
eyes |
| Disease features |
- |
| Remarks |
- |
| Date created |
2016-10-11 11:01:00 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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