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Summary Literature (0)
MIM:268200 - MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE

Xenbase Genes: lpin1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009992 - myoglobinuria, acute recurrent, autosomal recessive
MONDO:0020504 - hereditary recurrent myoglobinuria

Disease Ontology (DO):
DOID:0080108 - myoglobinuria