PRODH, proline dehydrogenase 1, 5625

N. diseases: 85; N. variants: 17
Disease: Amino Acid Metabolism, Inborn Errors ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		0.300 Biomarker group CTD_human Early neurological phenotype in 4 children with biallelic PRODH mutations. 17412540 2007