Disease association ontology term - MONDO:0020714 - mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy

Term summary

ID: MONDO:0020714
Name: mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy
Ontology or CV name: Disease association

Parents

is_a inborn mitochondrial myopathy
is_a fatal multiple mitochondrial dysfunctions syndrome

Annotation

Disease association

MONDO:0020714 - mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy

References:

PB_REF:0000006

Genes:

etp1 (SPAC22E12.10c)