|
limb-girdle muscular dystrophy type 2N
|
13162 |
|
|
limb-girdle muscular dystrophy type 2O
|
13161 |
|
|
congenital muscular dystrophy-POMT2 related
|
13160 |
|
|
congenital muscular dystrophy-dystroglycanopathy with intellectual disability type B2
|
13160 |
|
|
congenital muscular dystrophy-dystroglycanopathy with mental retardation type B2
|
13160 |
|
|
RBM20 familial isolated dilated cardiomyopathy
|
13168 |
|
|
muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related
|
13162 |
|
|
autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMGNT1
|
13161 |
|
|
autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMT2
|
13162 |
|
|
autosomal recessive limb-girdle muscular dystrophy type 2N
|
13162 |
|
|
autosomal recessive limb-girdle muscular dystrophy type 2O
|
13161 |
|
|
muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT1-Related
|
http://purl.obolibrary.org/obo/MONDO_0013161 |
|
|
muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT1-related
|
13161 |
|
|
muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-Related
|
http://purl.obolibrary.org/obo/MONDO_0013162 |
|
|
muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-related
|
13162 |
|
