Gene table: search width pubmed_id = 27858739


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

protein
All allelic disease phenotypes - locus/disease symbols
Klippel-Feil syndrome with Nemalin myopathy and facial dysmorphism - (AR)
3.12
27858739
MYO18B (22q12.1)
Myosin XVIIIB
* Nemaline Myopathy with Cardiomyopathy
* Klippel-Feil syndrome with Nemalin myopathy and facial dysmorphism - KFS4