|
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1; MDDGB1
|
http://purl.obolibrary.org/obo/MONDO_0013159 |
|
|
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 3
|
13155 |
|
|
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 3; MDDGB3
|
http://purl.obolibrary.org/obo/MONDO_0013155 |
|
|
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B1
|
13159.0 |
|
|
muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B3
|
13155.0 |
|
|
muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B, 4
|
13156 |
|
|
muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4
|
13156 |
|
|
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4
|
13156 |
|
|
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4; MDDGB4
|
http://purl.obolibrary.org/obo/MONDO_0013156 |
|
|
muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B4
|
13156.0 |
|
|
PARKINSONISM-dystonia, infantile; PKDYS
|
http://purl.obolibrary.org/obo/MONDO_0013150 |
|
|
cardiovascular malfunction arising from mental factors
|
1315 |
|
|
early onset autosomal recessive inflammatory bowel disease 28
|
13153 |
|
|
muscular dystrophy, congenital, Fktn-Related
|
http://purl.obolibrary.org/obo/MONDO_0013156 |
|
|
muscular dystrophy, congenital, Fktn-related
|
13156 |
|
