Inborn disorder of lysine, hydroxylysine, and tryptophan metabolism
MONDO:0800157A disorder of amino acid metabolism that has its basis in the disruption of the metabolism of lysine, hydroxylysine, and/or tryptophan.
0 clinical trials for this condition and its sub-types, 0 tagged with Inborn disorder of lysine, hydroxylysine, and tryptophan metabolism itself.
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Including sub-types (0)
Tagged with Inborn disorder of lysine, hydroxylysine, and tryptophan metabolism (0)
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