Disease #01277 (OPA+ (atrophy, optic, plus syndrome (OPA+)), OMIM:125250)
| Official abbreviation |
OPA+ |
| Name |
atrophy, optic, plus syndrome (OPA+) |
| OMIM ID |
125250 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
OPA1 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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