EXD3

exonuclease 3'-5' domain containing 3
ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red EXD3 in Cataract


Level 2: Ophthalmological disorders
Version 0.532

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • Cataract, MONDO:0005129, EXD3-related

Red EXD3 in Mendeliome


Version 1.3936

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Cataract, MONDO:0005129, EXD3-related