Disease #04436 (MDDGA9 (dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A9), OMIM:616538)
| Official abbreviation |
MDDGA9 |
| Name |
dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A9 |
| OMIM ID |
616538 |
| 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 |
DAG1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-09-23 10:25:22 +02:00 (CEST) |
| Date last edited |
2024-01-12 21:35:59 +01:00 (CET) |
Individuals
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