Gene table: search width pubmed_id = 32367058


Grey lines background indicate newly added items
Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Sorbitol dehydrogenase deficiency with peripheral neuropathy (CMT2 AR) - (AR)
14.98
32367058
SORD (15q21.1)
Sorbitol Dehydrogenase
* Sorbitol dehydrogenase deficiency with peripheral neuropathy - SORDD
* Neuropathy, hereditary motor, autosomal recessive 8 - HMNR8