Disease #00157

Official abbreviation 500003
Name STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL
OMIM ID 500003
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MT-ATP6
Associated tissues -
Disease features -
Remarks -

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