Condition: Gait abnormality


rs1557055405 in ABCD1 gene and Gait abnormality PMID 9452087 1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.

rs778361520 in ADGRB2 gene and Gait abnormality PMID 28891236 2017 A disease-associated mutation in the adhesion GPCR BAI2 (ADGRB2) increases receptor signaling activity.

rs387906905 in TRPV4 gene and Gait abnormality PMID 21288981 2011 TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies.