Disease: Sensorimotor neuropathy ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		0.010 GeneticVariation disease BEFREE Novel mutations in HINT1 gene cause autosomal recessive axonal neuropathy with neuromyotonia in two cases of sensorimotor neuropathy and one case of motor neuropathy. 30001929 2018