Cerebral cavernous malformation 2
MONDO:0011304Any familial cerebral cavernous malformation in which the cause of the disease is a mutation in the CCM2 gene.
Also known as: CCM2, CCM2 familial cerebral cavernous malformation, cerebral cavernous malformation 2, cerebral cavernous malformation type 2, cerebral cavernous malformations type 2, cerebral cavernous malformations-2, familial cerebral cavernous malformation caused by mutation in CCM2, cerebral cavernous malformations 2
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Disease
(618)
Nervous system disorder
(217)
Hereditary disease
(172)
Human disease
(14)
Hereditary neurological disease
(5)
Cerebral cavernous malformation
(2)
Disease of genetic or genomic mechanism
(2)
Congenital nervous system disorder
(1)
Disease by body system or component
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Disease by etiologic mechanism
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