Prolidase deficiency
MONDO:0008221An 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.
Follow this condition — get notified about new trialsBroader categories
Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
Disorder of peptide and amine metabolism
(0)
Inborn disorder of peptide metabolism
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.