Disease #00041 (PEOA3 (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 3 (PEOA-3)), OMIM:609286)
Official abbreviation |
PEOA3 |
Name |
ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 3 (PEOA-3) |
OMIM ID |
609286 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
C10orf2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-08-30 16:46:02 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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