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MIRAGE
muscular dystrophy-dystroglycanopathy type B6
Summary
- Synonym
-
- MDC1D
- MDDGB6
- congenital muscular dystrophy LARGE-related
- congenital muscular dystrophy type 1D
- muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6
- muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6
- Definition
- A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with mental retardation and structural brain abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the LARGE gene on chromosome 22q12.
- Super Class
- autosomal recessive disease muscular dystrophy-dystroglycanopathy type B
External Links
- Disease Ontology
- DOID:0110637
- ORDO
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O95461 | Xylosyl- and glucuronyltransferase LARGE1 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| D9IG22 | LARGE-1 (Fragment) |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000252 | Microcephaly |
| HP:0000028 | Cryptorchidism |
| HP:0000054 | Micropenis |
| HP:0000478 | Abnormality of the eye |
| HP:0000486 | Strabismus |
| HP:0000545 | Myopia |
| HP:0000580 | Pigmentary retinopathy |
| HP:0000707 | Abnormality of the nervous system |
| HP:0001249 | Intellectual disability |
| HP:0001263 | Global developmental delay |
