Disease Information |
Disease Name |
Gene Name |
Type |
UMLS |
Association Type |
Score |
Source |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
HTRA1 |
disease |
C1838577 |
CausalMutation |
0.8 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
HTRA1 |
disease |
C1838577 |
GermlineCausalMutation |
0.8 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
HTRA1 |
disease |
C1838577 |
AlteredExpression |
0.8 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
HTRA1 |
disease |
C1838577 |
GeneticVariation |
0.8 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
HTRA1 |
disease |
C1838577 |
Biomarker |
0.8 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
FN1 |
disease |
C1838577 |
GeneticVariation |
0.02 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
FN1 |
disease |
C1838577 |
AlteredExpression |
0.02 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
COL4A1 |
disease |
C1838577 |
GeneticVariation |
0.02 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
TGFB1 |
disease |
C1838577 |
AlteredExpression |
0.02 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
TGFB1 |
disease |
C1838577 |
Biomarker |
0.02 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
SMG8 |
disease |
C1838577 |
GeneticVariation |
0.01 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
LTBP1 |
disease |
C1838577 |
Biomarker |
0.01 |
disgenet |
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
CTSA |
disease |
C1838577 |
GeneticVariation |
0.01 |
disgenet |
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