Disease #05499 (OPA5 (atrophy, optic, type 5 (OPA-5)), OMIM:610708)
Official abbreviation |
OPA5 |
Name |
atrophy, optic, type 5 (OPA-5) |
OMIM ID |
610708 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
DNM1L |
Associated tissues |
- |
Disease features |
autosomal dominant |
Remarks |
- |
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