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Summary Literature (0)
DOID:0080108 - myoglobinuria

Disease Ontology Definition:A myopathy that is characterized by an increased urinary excretion of myoglobin.

Synonyms:

Xenbase Genes : lpin1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0000866 - hereditary myoglobinuria


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

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