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Summary Literature (0)
MIM:613116 - THROMBOPHILIA DUE TO HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY; THPH11

Xenbase Genes: hrg

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013143 - hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

Disease Ontology (DO):
DOID:0111903 - thrombophilia due to HRG deficiency