Disease #04292 (MDDGA12 (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A12 (MDDGA-12)), OMIM:615249)
| Official abbreviation |
MDDGA12 |
| Name |
dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A12 (MDDGA-12) |
| OMIM ID |
615249 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
POMK |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-06-19 22:43:00 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|