RARG

retinoic acid receptor gamma
OMIM: 180190, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red RARG in Mendeliome


Version 1.4693

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Ectodermal dysplasia syndrome, MONDO:0019287, RARG-related

Red RARG in Ectodermal Dysplasia


Level 2: Dermatological disorders
Version 0.110

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • Ectodermal dysplasia syndrome, MONDO:0019287, RARG-related