Disease #01442

Official abbreviation PEOA-1
Name ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 1 (PEOA-1)
OMIM ID 157640
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene POLG
Associated tissues -
Disease features -
Remarks -