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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:
Echinobase Genes
:
pus1
| 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
Parent(s):
mitochondrial myopathy (is_a),
myopathy (is_a)