Gene table: search width pubmed_id = 30770808


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

protein
All allelic disease phenotypes - locus/disease symbols
Myopathy, congenital proximal with minicore lesions - (AR)
3.59
30770808
FXR1 (3q26.33)
FMR1 autosomal homolog
* Myopathy, congenital proximal with minicore lesions - MYOPMIL
* Myopathy, congenital with respitory insufficiency and bone fractures - MYORIBF