Disease #00158

Official abbreviation MMIT
Name MITOCHONDRIAL MYOPATHY, INFANTILE, TRANSIENT;MMIT
OMIM ID 500009
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MT-TE
Associated tissues -
Disease features -
Remarks -

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