Disease #01098 (MDDGB-4 (dystrophy, muscular, dystroglycanopathy (congenital without mental retardation), type B4 (MDDGB-4)), OMIM:613152)
| Official abbreviation |
MDDGB-4 |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital without mental retardation), type B4 (MDDGB-4) |
| OMIM ID |
613152 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FKTN |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
