Disease #05852 (MDDGB15 (dystrophy, muscular, dystroglycanopathy (congenital with impaired intellectual development), type B15 (MDDGB15)), OMIM:618992)
| Official abbreviation |
MDDGB15 |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital with impaired intellectual development), type B15 (MDDGB15) |
| OMIM ID |
618992 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
DPM3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|
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