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, 0 tagged with Disorder of peptide and amine metabolism itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Disorder of peptide and amine metabolism
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Disorder of methylamine metabolism 0 trials · 2 incl. sub-types
2 sub-types
- Dimethylglycine dehydrogenase deficiency 0 trials · 2 incl. sub-types Sub-types →
- Sarcosinemia 0 trials
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Disorder of polyamine metabolism 0 trials · 1 incl. sub-types
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Inherited glutathione metabolism disease 0 trials · 1 incl. sub-types
6 sub-types
- Inherited glutathione synthetase deficiency 1 trial Sub-types →
- 5-oxoprolinase deficiency 0 trials
- Gamma-glutamyl transpeptidase deficiency 0 trials
- Gamma-glutamylcysteine synthetase deficiency 0 trials
- Hemolytic anemia due to glutathione reductase deficiency 0 trials
- Spondylometaphyseal dysplasia, Sedaghatian type 0 trials
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3 sub-types
- Homocarnosinosis 0 trials Sub-types →
- Late-onset nephronophthisis 0 trials
- Prolidase deficiency 0 trials
Most studied deeper sub-types
Trimethylaminuria
(2)
Glutathione synthetase deficiency with 5-oxoprolinuria
(1)
Carnosinemia
(0)
Glutathione synthetase deficiency without 5-oxoprolinuria
(0)
Keratosis follicularis spinulosa decalvans, autosomal dominant
(0)
Keratosis follicularis spinulosa decalvans, X-linked
(0)
Secondary trimethylaminuria
(0)
Severe primary trimethylaminuria
(0)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.