rs2904552, PRODH

N. diseases: 3
Disease: Proline dehydrogenase deficiency ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.800 GeneticVariation UNIPROT Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. 17135275 2007
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.800 GeneticVariation UNIPROT Functional consequences of PRODH missense mutations. 15662599 2005
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.800 GeneticVariation UNIPROT PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. 12217952 2002
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.800 SusceptibilityMutation CLINVAR
Proline dehydrogenase deficiency
CUI: C0268529
Disease: Proline dehydrogenase deficiency
0.800 CausalMutation CLINVAR