| Disease phenotype | Item
in
this
table | Key
references | Gene symbol (chromosome)
protein | All allelic disease phenotypes - locus/disease symbols |
| LGMD related to KBTBD13 - (AD) | 1.22 | | | | * 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 |
|
| Muscular dystrophy, limb-girdle, autosomal recessive 7
(Formerly LGMD2G - (AR) | 1.30 | | | | * 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 |
|
| Muscular dystrophy-dystroglycanopathy (Limb-girdle), type C4 - (AR) | 1.46 | | | | * 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 |
|
