MOCS3

molybdenum cofactor synthesis 3
OMIM: 609277, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber MOCS3 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.26
Latest signed off version: v8.0 (12 Aug 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Amber
Phenotypes
  • Molybdenum cofactor deficiency, type B2, OMIM:621373