Gene table: search width pubmed_id = 23777631


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Charcot-Marie-Tooth disease, recessive intermediate, C - (AR)
14.25
23777631
23844677
PLEKHG5 (1p36)
Pleckstrin homology domain containing, family G (with RhoGef domain) member 5
* spinal muscular atrophy, distal, autosomal recessive, 4 - DSMA4
* Axonal neuropathy intermediate recessive C - CMTRIC