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Hereditary neuropathy with liability to pressure palsies
Hereditary neuropathy with liability to pressure palsies
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES
162500
PMP22
Unknown
—
HPO
EGR2 and SOX10-mediated initiation of Schwann cell myelination
TOMACULOUS NEUROPATHY
MESH:C536965
PMP22
Unknown
12796555
15205993
9748013
CTD
,
ClinGen
EGR2 and SOX10-mediated initiation of Schwann cell myelination
All
1
Causal
0
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
1
HPO
1
GWAS catalog
0
GenCC
0
ClinGen
1
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Charcot-Marie-Tooth disease type 1A
1 shared gene
PMP22
Related via 1 shared gene including PMP22.
Paresthesia
1 shared gene
PMP22
Related via 1 shared gene including PMP22.
Hereditary sensory and motor neuropathy
1 shared gene
PMP22
Related via 1 shared gene including PMP22.
Demyelinating diseases
1 shared gene
PMP22
Related via 1 shared gene including PMP22.
Myoclonic epilepsy
1 shared gene
PMP22
Related via 1 shared gene including PMP22.
1
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