DHRS3

dehydrogenase/reductase 3
OMIM: 612830, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber DHRS3 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 0.522

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Syndromic disease, MONDO:0002254, DHRS3-related

Amber DHRS3 in Craniosynostosis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.74

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Syndromic disease, MONDO:0002254, DHRS3-related

Amber DHRS3 in Mendeliome


Version 1.4215

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Syndromic disease, MONDO:0002254, DHRS3-related

Amber DHRS3 in Fetal anomalies


Version 1.522

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Syndromic disease, MONDO:0002254, DHRS3-related