Disease #03738 (MDDGA8 (dystrophy-dystroglycanopathy, muscular, congenital with brain and eye anomalies), type A8), OMIM:614830)
Official abbreviation |
MDDGA8 |
Name |
dystrophy-dystroglycanopathy, muscular, congenital with brain and eye anomalies), type A8 |
OMIM ID |
614830 |
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 |
POMGNT2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2024-01-12 21:18:14 +01:00 (CET) |
Individuals
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