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Likely inborn error of metabolism - targeted testing not possible v4.123 PRODH Arina Puzriakova Phenotypes for gene: PRODH were changed from Hyperprolinemia, type I, OMIM; 239500; hyperprolinemia type 1, MONDO:0009400 to Hyperprolinemia, type I, OMIM:239500; hyperprolinemia type 1, MONDO:0009400
Likely inborn error of metabolism - targeted testing not possible v2.255 PRODH Sarah Leigh Phenotypes for gene: PRODH were changed from Hyperprolinemia, type I 239500; Hyperprolinaemia type I (Disorders of ornithine or proline metabolism) to Hyperprolinemia, type I, OMIM; 239500; hyperprolinemia type 1, MONDO:0009400
Likely inborn error of metabolism - targeted testing not possible v2.254 PRODH Sarah Leigh Classified gene: PRODH as Green List (high evidence)
Likely inborn error of metabolism - targeted testing not possible v2.254 PRODH Sarah Leigh Added comment: Comment on list classification: Evidence for the association of PRODH variants with Hyperprolinemia, type I, OMIM; 239500 has been classified as Definitive by ClinGen Aminoacidopathy Gene Curation Expert Panel on 04/27/2021
(https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_5f28c677-a9b4-4bb3-9aed-14af97ad9896-2021-04-27T160000.000Z).
Likely inborn error of metabolism - targeted testing not possible v2.254 PRODH Sarah Leigh Gene: prodh has been classified as Green List (High Evidence).
Likely inborn error of metabolism - targeted testing not possible v1.47 PRODH Ivone Leong Source NHS GMS was added to PRODH.
Source London North GLH was added to PRODH.
Likely inborn error of metabolism - targeted testing not possible v0.4 PRODH Ellen McDonagh gene: PRODH was added
gene: PRODH was added to Inborn errors of metabolism. Sources: Expert Review Green
Mode of inheritance for gene: PRODH was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PRODH were set to 27604308; 24816252
Phenotypes for gene: PRODH were set to Hyperprolinemia, type I 239500; Hyperprolinaemia type I (Disorders of ornithine or proline metabolism)