Cerebral cavernous malformation 3
MONDO:0011305Any familial cerebral cavernous malformation in which the cause of the disease is a mutation in the PDCD10 gene.
Also known as: CCM3, PDCD10 familial cerebral cavernous malformation, cerebral cavernous malformation 3, cerebral cavernous malformation type 3, cerebral cavernous malformations 3, cerebral cavernous malformations type 3, cerebral cavernous malformations-3, familial cerebral cavernous malformation caused by mutation in PDCD10
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Disease
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Nervous system disorder
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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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