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- B36b81ca3371329ec2250b2b26d86fe1d hasDbXref "https://orcid.org/0000-0002-0736-9199" @default.
- B36b81ca3371329ec2250b2b26d86fe1d type Axiom @default.
- B36b81ca3371329ec2250b2b26d86fe1d annotatedProperty IAO_0000115 @default.
- B36b81ca3371329ec2250b2b26d86fe1d annotatedSource MONDO_0007691 @default.
- B36b81ca3371329ec2250b2b26d86fe1d annotatedTarget "A form of Guillain-Barre syndrome (GBS) that occurs in persons or families with a genetic predisposition to the acute or chronic forms of GBS. Note that GBS is considered to be a complex multifactorial disorder with both genetic and environmental factors, and families with clear Mendelian inheritance have been rarely reported: a mutation in the PMP22 gene (601097) on chromosome 17 was identified in a single family with the acute (AIDP) and chronic (CIDP) forms of inflammatory demyelinating polyneuropathy." @default.