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Summary Literature (0)
MIM:238710 - HYPERLYSINEMIA DUE TO DEFECT IN LYSINE TRANSPORT INTO MITOCHONDRIA

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009388 - hyperlysinemia
MONDO:0009389 - hyperlysinemia due to defect in lysine transport into mitochondria

Disease Ontology (DO):
DOID:9274 - hyperlysinemia