CCER2

coiled-coil glutamate rich protein 2
OMIM: 617634, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber CCER2 in Cerebral vascular malformations


Level 2: Neurology
Version 4.10
Latest signed off version: v4.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Moyamoya Disease, MONDO:0016820