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prolidase deficiency (DOID:0111540)
Alliance: disease page
Synonyms: hyperimidodipeptiduria; imidodipeptidase deficiency; peptidase deficiency
Alt IDs: OMIM:170100, MESH:D056732, NCI:C85029, ORDO:742, UMLS_CUI:C0268532
Definition: An amino acid metabolic disorder characterized by massive imidodipeptiduria, chronic and slowly healing ulcerations, recurrent infections, dysmorphic facial features, variable cognitive impairment, splenomegaly, and lack of or reduced prolidase activity that has_material_basis_in homozygous or compound heterozygous mutation in the PEPD gene on chromosome 19q13.11.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory