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Summary Literature (0)
DOID:0080099 - myopathy, lactic acidosis, and sideroblastic anemia


Disease Ontology Definition:A mitochondrial myopathy that is characterised by progressive exercise intolerance manifesting in childhood, onset of sideroblastic anaemia around adolescence, lactic acidaemia, and mitochondrial myopathy.

Synonyms:

Xenbase Genes : yars2, pus1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000863 - myopathy, lactic acidosis, and sideroblastic anemia

OMIM:
OMIM:600462 - MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1; MLASA1
OMIM:613561 - MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): mitochondrial myopathy (is_a), myopathy (is_a)