Disorder of peptide and amine metabolism
MONDO:0100473An inherited metabolic disease that has its basis in the disruption of peptide and/or amine metabolic process.
4 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Trimethylaminuria
(2)
Glutathione synthetase deficiency with 5-oxoprolinuria
(1)
Inherited glutathione synthetase deficiency
(1)
Syndromic X-linked intellectual disability Snyder type
(1)
5-oxoprolinase deficiency
(0)
Carnosinemia
(0)
Diaphyseal medullary stenosis-bone malignancy syndrome
(0)
Dimethylglycine dehydrogenase deficiency
(0)
Disorder of methylamine metabolism
(0)
Disorder of polyamine metabolism
(0)
Gamma-glutamylcysteine synthetase deficiency
(0)
Gamma-glutamyl transpeptidase deficiency
(0)
Glutathione synthetase deficiency without 5-oxoprolinuria
(0)
Hemolytic anemia due to glutathione reductase deficiency
(0)
Homocarnosinosis
(0)
Inborn disorder of peptide metabolism
(0)
Inherited glutathione metabolism disease
(0)
Keratosis follicularis spinulosa decalvans
(0)
Keratosis follicularis spinulosa decalvans, autosomal dominant
(0)
Keratosis follicularis spinulosa decalvans, X-linked
(0)