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MIRAGE
congenital muscular dystrophy-dystroglycanopathy type A14
Summary
- Synonym
-
- MDDGA14
- Walker-Warburg syndrome or muscle-eye-brain disease GMPPB-related
- congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A14
- Definition
- A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in in GMPPB on 3p21.31.
- Super Class
- congenital muscular dystrophy-dystroglycanopathy type A
External Links
- Disease Ontology
- DOID:0111233
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002540 | Inability to walk |
| HP:0003551 | Difficulty climbing stairs |
| HP:0001321 | Cerebellar hypoplasia |
| HP:0003623 | Neonatal onset |
| HP:0001562 | Oligohydramnios |
| HP:0001249 | Intellectual disability |
| HP:0003560 | Muscular dystrophy |
| HP:0001324 | Muscle weakness |
| HP:0011463 | Childhood onset |
| HP:0001251 | Ataxia |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 29954 | POMT2 | protein O-mannosyltransferase 2 |
| 10585 | POMT1 | protein O-mannosyltransferase 1 |
| 148789 | B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 |
| 2218 | FKTN | fukutin |
| 29925 | GMPPB | GDP-mannose pyrophosphorylase B |
| 55624 | POMGNT1 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) |
| 729920 | CRPPA | CDP-L-ribitol pyrophosphorylase A |
| 79147 | FKRP | fukutin related protein |
| 9215 | LARGE1 | LARGE xylosyl- and glucuronyltransferase 1 |
