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 5.1
Latest signed off version: v5.0 (6 May 2026)

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