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Summary Literature (0)
MIM:600627 - HYPERTRYPTOPHANEMIA; HYPTRP

Xenbase Genes: tdo2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010907 - familial hypertryptophanemia

Disease Ontology (DO):
DOID:0111703 - familial hypertryptophanemia