syndromic intellectual disability skin disorder prolidase deficiency https://github.com/monarch-initiative/mondo/issues/4985 https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/5682 https://www.malacards.org/card/prolidase_deficiency UMLS:C0268532 NCIT:C85029 DOID:0111540 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. hyperimidodipeptiduria NANDO:2200472 MONDO:0008221 icd11.foundation:1416203271 OMIM:170100 prolidase deficiency Imidodipeptidase deficiency MEDGEN:120647 SCTID:410055005 Orphanet:742 Peptidase deficiency MESH:D056732 GARD:0007473 inborn disorder of peptide metabolism obsolete syndromic lymphedema obsolete_prolidase deficiency