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cerebral cavernous malformation 2 | RareConnect | RareConnect.io

/famililal cerebral cavernous malformations

/cerebral cavernous malformation 2

cerebral cavernous malformation 2

Rare Disease

MONDO:0011304

Also Known As

CCM2CCM2 familial cerebral cavernous malformationcerebral cavernous malformation 2cerebral cavernous malformation type 2cerebral cavernous malformations type 2cerebral cavernous malformations-2familial cerebral cavernous malformation caused by mutation in CCM2cerebral cavernous malformations 2

Definition

Any familial cerebral cavernous malformation in which the cause of the disease is a mutation in the CCM2 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:603284 ↗

GARD

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