myoglobinuria

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: lpin1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0000866 - obsolete hereditary myoglobinuria

MONDO:0000866 - obsolete hereditary myoglobinuria

MIM:

MIM:268200 - MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE

MIM:268200 - MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): myopathy (is_a)