Disorder "Cerebral Cavernous Malformation"
Found 33 records
Disorder information
Disorder name:
Cerebral Cavernous Malformation 
Disoder ID:
Synonyms:
familial cavernous angioma, cavernous angiomatous malformations, cerebral capillary malformations 
Definition:
Cerebral cavernous malformations are collections of small blood vessels (capillaries) in the brain that are enlarged and irregular in structure. These capillaries have abnormally thin walls, and they lack other support tissues, such as elastic fibers, which normally make them stretchy. As a result, the blood vessels are prone to leakage, which can cause the health problems related to this condition. Cavernous malformations can occur anywhere in the body, but usually produce serious signs and symptoms only when they occur in the brain and spinal cord (which are described as cerebral). 
Modifier statisitcs
Record:
33 
Gene:
21 
Variant:
32 
Reference:
Effect type:
Pleiotropy(29) ,Expressivity(4)  
Modifier effect:
Association with lesion counts(16) ,Association with intracerebral hemorrhage(13) ,Risk factor(4)  
Modifier gene Variant Effect type Modifier effect Evidence Effect PubMed ID
TLR6 TLR6:rs73811240 Pleiotropy  Association with lesion counts  P=0.015  These results suggest that polymorphisms in inflammatory and immune response pathways contribute to variability in CCM1 disease severity and might be used as predictors of disease severity.more more
TLR4 TLR4:rs10759930 Pleiotropy  Association with lesion counts  P=0.0002  These results suggest that polymorphisms in inflammatory and immune response pathways contribute to variability in CCM1 disease severity and might be used as predictors of disease severity.more more
TGFBR2 TGFBR2:rs11924422 Pleiotropy  Association with lesion counts  P=0.007  These results suggest that polymorphisms in inflammatory and immune response pathways contribute to variability in CCM1 disease severity and might be used as predictors of disease severity.more more
TGFBR2:rs17025785 Pleiotropy  Association with intracerebral hemorrhage  P=0.003  These results suggest that polymorphisms in inflammatory and immune response pathways contribute to variability in CCM1 disease severity and might be used as predictors of disease severity.more more
TGFBR2:rs9823731 Pleiotropy  Association with intracerebral hemorrhage  P=0.009  These results suggest that polymorphisms in inflammatory and immune response pathways contribute to variability in CCM1 disease severity and might be used as predictors of disease severity.more more
TGFBR2:rs9823731 Pleiotropy  Association with lesion counts  P=0.011  These results suggest that polymorphisms in inflammatory and immune response pathways contribute to variability in CCM1 disease severity and might be used as predictors of disease severity.more more
SELS SELS:rs4965815 Pleiotropy  Association with intracerebral hemorrhage  P=0.009  These results suggest that polymorphisms in inflammatory and immune response pathways contribute to variability in CCM1 disease severity and might be used as predictors of disease severity.more more
PTGS2 COX-2:rs689462 Pleiotropy  Association with lesion counts  P=0.012  These results suggest that polymorphisms in inflammatory and immune response pathways contribute to variability in CCM1 disease severity and might be used as predictors of disease severity.more more
PDCD10 PDCD10:c.269-1G>A Expressivity  Risk factor  Pedigree analysis  The genetic variations could interfere with the proper CCM1/CCM2/CCM3 protein complex thus explaining the observed clinical variability.more more
MSR1 MSR1:rs62489577 Pleiotropy  Association with lesion counts  P=0.013  These results suggest that polymorphisms in inflammatory and immune response pathways contribute to variability in CCM1 disease severity and might be used as predictors of disease severity.more more
Total 33,Each Page
,Jump To
Page