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Hypokalemic periodic paralysis, type 2
Hypokalemic periodic paralysis, type 2
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Subtype of:
Periodic paralysis
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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
Hypokalemic periodic paralysis, type 2
MONDO_0008223
SCN4A
Causal
28779239
23801527
32978841
17998485
18166706
19118277
26700687
15534250
Open Targets
Phase 0 - rapid depolarisation
Hypokalemic periodic paralysis, type 2, 613
MONDO_0008223
SCN4A
Unknown
17395131
15534250
Open Targets
Phase 0 - rapid depolarisation
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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Related via 1 shared gene including SCN4A.
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Related via 1 shared gene including SCN4A.
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1 shared gene
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Related via 1 shared gene including SCN4A.
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1 shared gene
SCN4A
Related via 1 shared gene including SCN4A.
1
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