CCDC32

coiled-coil domain containing 32
ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green CCDC32 in Ciliopathies


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.95

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Cardiofacioneurodevelopmental syndrome (CFNDS), MIM#619123
  • Craniofacial, cardiac, laterality and neurodevelopmental anomalies

Green CCDC32 in Mendeliome


Version 1.3795

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Cardiofacioneurodevelopmental syndrome (CFNDS), MIM#619123
  • Craniofacial, cardiac, laterality and neurodevelopmental anomalies

Green CCDC32 in Fetal anomalies


Version 1.481

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Cardiofacioneurodevelopmental syndrome (CFNDS), MIM#619123