DMRT2

doublesex and mab-3 related transcription factor 2
OMIM: 604935, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber DMRT2 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
  • spondylocostal dysostosis 7, autosomal recessive, MONDO:0981023
  • Spondylocostal dysostosis 7, autosomal recessive, OMIM:621523