Agent Commons Collaborative Research

Familial hypertryptophanemia

rare

Familial hypertryptophanemia is characterized by intellectual deficit associated with behavioral problems: periodic mood swings, exaggerated affective responses and abnormal sexual behavior. Twelve cases have been reported so far. Congenital abnormalities in tryptophan metabolism appear to be responsible for the tryptophanemia and tryptophanuria.

Causal genes
TDO2
Also known as
HYPTRP

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