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Aicardi-goutieres syndrome 1, dominant and recessive
Aicardi-goutieres syndrome 1, dominant and recessive
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Subtype of:
Aicardi goutieres syndrome
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Show by gene
(one row per gene, with all of its disease terms together)
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Aicardi-Goutieres syndrome 1, dominant and recessive
MONDO_0009165
TREX1
Unknown
15254239
36581356
39472908
17846997
18583934
29239743
15883328
17357087
16845398
17660818
28334938
27159321
25527826
20301621
24357685
25604658
27411419
25655951
21808053
20799324
Open Targets
Cytosolic DNA-sensing pathway
Regulation by TREX1
IRF3-mediated induction of type I IFN
Aicardi-Goutieres syndrome 1, dominant and recessive AR, AD
MONDO_0009165
TREX1
Unknown
17660820
18204807
16845398
23881107
12525718
Open Targets
Cytosolic DNA-sensing pathway
Regulation by TREX1
IRF3-mediated induction of type I IFN
All
1
Causal
0
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
1
Related Diseases
Diseases that share the most curated genes with Aicardi-goutieres syndrome 1, dominant and recessive.
5
View disease cluster →
Type i interferonopathy
1 shared gene
TREX1
Related via 1 shared gene including TREX1.
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
1 shared gene
TREX1
Related via 1 shared gene including TREX1.
Cerebroretinal vasculopathy
1 shared gene
TREX1
Related via 1 shared gene including TREX1.
Hereditary endotheliopathy, retinopathy, nephropathy and stroke
1 shared gene
TREX1
Related via 1 shared gene including TREX1.
Retinal vasculopathy with cerebral leukodystrophy
1 shared gene
TREX1
Related via 1 shared gene including TREX1.
1
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