Disease #00816 (MDDGA6 (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A6 (MDDGA-6)), OMIM:613154)
| Official abbreviation |
MDDGA6 |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A6 (MDDGA-6) |
| OMIM ID |
613154 |
| 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 |
LARGE |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|
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