Gene table: search width pubmed_id = 15121789


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

protein
All allelic disease phenotypes - locus/disease symbols
Muscular dystrophy-dystroglycanopathy (Congenital with brain and eyes anomlies), type A5 - (AR)
2.22
15121789
FKRP (19q13.32)
Fukutin-related protein
* Walker-Warburg syndrome - WWS
* Muscle-eye-brain disease - MEB
* Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), - MDDGA5
* Muscular dystrophy-dystroglycanopathy (congenital with or without mental retarda - MDDGB5
* Muscular dystrophy, limb-girdle, type 2I - LGMD2I