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
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|