Disease #04646

Official abbreviation PEOB-2
Name ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal recessive, type 2 (PEOB-2)
OMIM ID 616479
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene RNASEH1
Associated tissues -
Disease features -
Remarks -