Disease #00534

Official abbreviation 616479
Name Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2, 616479 (3)
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 -

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