Gene table: search width pubmed_id = 17036286


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

protein
All allelic disease phenotypes - locus/disease symbols
Dilated cardiomyopathy related, 1X - (AR)
10.61
17036286
FKTN (9q31-q33)
Fukutin
* Walker-Warburg syndrome - WWS
* Muscular dystrophy-dystroglycanopathy (congenital without mental retardation), t - MDDGB4
* fukuyama congenital muscular dystrophy - FCMD
* Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), - MDDGA4
* Cardiomyopathy, dilated, 1X - CMD1X
* Limb-Girdle, Muscular dystrophy, type 2M - LGMD2M