SLC52A2, solute carrier family 52 member 2, 79581

N. diseases: 261; N. variants: 21
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 		0.110 GeneticVariation disease BEFREE We used both exome and Sanger sequencing to identify SLC52A2 mutations in patients presenting with cranial neuropathies and sensorimotor neuropathy with or without respiratory insufficiency. 24253200 2014
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		0.110 Biomarker disease HPO