Gene table: search width pubmed_id = 22101682


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

protein
All allelic disease phenotypes - locus/disease symbols
Congenital myopathy 10A, severe variant - (AR)
3.29
22101682
MEGF10 (5q23.2)
Multiple EGF-like-domains 10
* Congenital myopathy 10A, severe variant - CMYP10A
* Congenital myopathy 10B, mild variant - CMYP10B