Disease #00027 (OPA (Optic Atrophy), OMIM:165500)
Official abbreviation |
OPA |
Name |
Optic Atrophy |
OMIM ID |
165500 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
296 |
Phenotype entries for this disease |
- |
Associated with 5 genes |
AFG3L2, MFN2, OPA1, OPA3, SLC25A46 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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