Prolidase deficiency

MONDO:0008221

An inherited disorder of peptide metabolism characterized by severe skin lesions, recurrent infections (involving mainly the skin and respiratory system), dysmorphic facial features, variable cognitive impairment, and splenomegaly.

Also known as: hyperimidodipeptiduria, prolidase deficiency, Imidodipeptidase deficiency, Peptidase deficiency

0 clinical trials for this condition and its sub-types, 0 tagged with Prolidase deficiency itself.

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↑ Inborn disorder of peptide metabolism (0)

Including sub-types (0) Tagged with Prolidase deficiency (0)

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