Disease #01101 (MDDGB1 (dystrophy-dystroglycanopathy, muscular, (congenital with mental retardation), type B1), OMIM:613155)
Official abbreviation |
MDDGB1 |
Name |
dystrophy-dystroglycanopathy, muscular, (congenital with mental retardation), type B1 |
OMIM ID |
613155 |
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 |
POMT1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2024-01-12 21:48:57 +01:00 (CET) |
Individuals
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