Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

GUILLAIN-BARRE SYNDROME, FAMILIAL
Synonyms

CIDP
ID

http://purl.bioontology.org/ontology/OMIM/139393
altLabel

CIDP

AIDP

GBS

POLYNEUROPATHY, INFLAMMATORY DEMYELINATING, CHRONIC

POLYNEUROPATHY, INFLAMMATORY DEMYELINATING, ACUTE
cui

C3542501

C0393819

C4083008
Gene Locus

17p11.2
Gene Symbol

CMT1E

CIDP

PMP22

CMT1A

DSS
MIMTYPEMEANING

Phenotype description, molecular basis known.
notation

139393
OMIM Entry Type

3
OMIM MimType Value

pound
prefLabel

GUILLAIN-BARRE SYNDROME, FAMILIAL
tui

T047
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http://purl.bioontology.org/ontology/MEDLINEPLUS/C3542501 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/ICD10CM/G61.81 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MESH/D020275 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/D020275 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/D020277 Medical Subject Headings CUI