Disease #03846 (MDDGA11 (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A11 (MDDGA-11)), OMIM:615181)
| Official abbreviation |
MDDGA11 |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A11 (MDDGA-11) |
| OMIM ID |
615181 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 1 gene |
B3GALNT2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|
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