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MIRAGE
autosomal recessive limb-girdle muscular dystrophy type 2P
Summary
- Synonym
-
- LGMD2P
- MDDGC9
- muscular dystrophy-dystroglycanopathy (limb-girdle) type C9
- muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related
- Definition
- An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gene encoding alpha-dystroglycan (DAG1) on chromosome 3p21.
- Super Class
- autosomal recessive limb-girdle muscular dystrophy
External Links
- Disease Ontology
- DOID:0110293
- Mondo Disease Ontology
- ORDO
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q14118 | Dystroglycan 1 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q62165 | Dystroglycan 1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003391 | Gowers sign |
| HP:0002465 | Poor speech |
| HP:0006785 | Limb-girdle muscular dystrophy |
| HP:0001270 | Motor delay |
| HP:0003707 | Calf muscle pseudohypertrophy |
| HP:0010864 | Intellectual disability, severe |
| HP:0002938 | Lumbar hyperlordosis |
| HP:0001256 | Intellectual disability, mild |
| HP:0003236 | Elevated circulating creatine kinase concentration |
| HP:0006466 | Ankle flexion contracture |
