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DOID:0080099 - myopathy, lactic acidosis, and sideroblastic anemia
Disease Ontology Definition:A mitochondrial myopathy that is characterized by progressive exercise intolerance manifesting in childhood, onset of sideroblastic anaemia around adolescence, lactic acidaemia, and mitochondrial myopathy.
Synonyms:
Xenbase Genes
:
yars2,
pus1
| MONDO:0000863 - myopathy, lactic acidosis, and sideroblastic anemia |
| MIM:600462 - MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 1; MLASA1 |
| MIM:613561 - MYOPATHY, LACTIC ACIDOSIS, AND SIDEROBLASTIC ANEMIA 2; MLASA2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
mitochondrial myopathy (is_a),
myopathy (is_a)