CCM2

CCM2 scaffold protein
OMIM: 607929, ClinGen, DECIPHER

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green CCM2 in Mendeliome


Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Cerebral cavernous malformations-2 MIM#603284

Red CCM2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review Red
  • Expert Review
Phenotypes
  • Cerebral cavernous malformations-2, MIM#603284

Amber CCM2 in Vascular Malformations_Germline


Level 2: Cardiovascular disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Royal Melbourne Hospital
Phenotypes
  • Cerebral cavernous malformations-2, MIM# 603284
Tags
  • SV/CNV

Green CCM2 in Stroke


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review Green
  • Literature
Phenotypes
  • Cerebral cavernous malformations-2 MIM#603284

Green CCM2 in Cerebral vascular malformations


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Genomics England PanelApp
  • Expert Review Green
Phenotypes
  • Cerebral cavernous malformations 2
  • Cerebral Cavernous Malformation
  • Capillary malformation-arteriovenous malformation 608354
  • Cerebral Cavernous Malformations