Disease #01108 (MDDGB-2 (dystrophy, muscular, dystroglycanopathy (congenital with mental retardation), type B2 (MDDGB-2)), OMIM:613156)
| Official abbreviation |
MDDGB-2 |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital with mental retardation), type B2 (MDDGB-2) |
| OMIM ID |
613156 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
POMT2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
