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famililal cerebral cavernous malformations

Disease Summary
Associated Targets (3)
Tbio

3


Mondo Description A rare evolutive vascular malformation disorder characterized by closely clustered irregular dilated capillaries that can be asymptomatic or that can cause variable neurological manifestations such as seizures, non-specific headaches, progressive or transient focal neurologic deficits, and/or cerebral hemorrhages.
Mondo Term and Equivalent IDs
MONDO:0031037:  famililal cerebral cavernous malformations
OMIMPS:116860: 
Orphanet:221061: 
SCTID:717003001: 
UMLS:C2931263: