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Meckel syndrome 6
Meckel syndrome 6
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Subtype of:
Meckel-gruber 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
Meckel syndrome 6
MONDO_0012848
CC2D2A
Unknown
18513680
18950740
19466712
19574260
19777577
23351400
24706459
27959436
31411728
Open Targets
Anchoring of the basal body to the plasma membrane
MKS6
MONDO_0012848
CC2D2A
Unknown
19777577
18513680
Open Targets
Anchoring of the basal body to the plasma membrane
All
1
Causal
1
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
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Diseases that share the most curated genes with Meckel syndrome 6.
5
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Coach syndrome
1 shared gene
CC2D2A
Related via 1 shared gene including CC2D2A.
Encephalocele
1 shared gene
CC2D2A
Related via 1 shared gene including CC2D2A.
Arima syndrome
1 shared gene
CC2D2A
Related via 1 shared gene including CC2D2A.
Anencephaly
1 shared gene
CC2D2A
Related via 1 shared gene including CC2D2A.
Congenital clubfoot
1 shared gene
CC2D2A
Related via 1 shared gene including CC2D2A.
1
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