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MIRAGE
autosomal recessive limb-girdle muscular dystrophy type 2U
Summary
- Synonym
-
- LGMD2U
- MDDGC7
- autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency
- muscular dystrophy limb-girdle type 2U
- muscular dystrophy-dystroglycanopathy (limb-girdle) type C7
- Definition
- An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the ISPD gene on chromosome 7p21.
- Super Class
- autosomal recessive limb-girdle muscular dystrophy
External Links
- Disease Ontology
- DOID:0110295
- Mondo Disease Ontology
- ORDO
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q5RJG7 | D-ribitol-5-phosphate cytidylyltransferase |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003326 | Myalgia |
| HP:0002505 | Loss of ambulation |
| HP:0008994 | Proximal muscle weakness in lower limbs |
| HP:0000478 | Abnormality of the eye |
| HP:0003707 | Calf muscle pseudohypertrophy |
| HP:0011446 | Abnormality of mental function |
| HP:0003202 | Skeletal muscle atrophy |
| HP:0000158 | Macroglossia |
| HP:0003325 | Limb-girdle muscle weakness |
| HP:0008305 | Exercise-induced myoglobinuria |
