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 |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
LARGE |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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