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Guillain-Barre syndrome, familial

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description A chronic monophasic, progressive or relapsing symmetric sensorimotor disorder characterized by progressive muscular weakness with impaired sensation, absent or diminished tendon reflexes and elevated cerebrospinal fluid (CSF) proteins.
Uniprot Description Putative autoimmune disorder presenting in an acute (AIDP) or chronic form (CIDP). The acute form is also known as Guillain-Barre syndrome.
Mondo Term and Equivalent IDs
MONDO:0007691:  Guillain-Barre syndrome, familial
GARD:0006102: 
SCTID:716723000: