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congenital muscular dystrophy-dystroglycanopathy type A2
Summary
- Synonym
-
- MDDGA2
- Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related
- congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2
- Definition
- A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in POMT2 on 14q24.3.
- Super Class
- congenital muscular dystrophy-dystroglycanopathy type A
External Links
- Disease Ontology
- DOID:0111240
- Mondo Disease Ontology
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001324 | Muscle weakness |
| HP:0001328 | Specific learning disability |
| HP:0001331 | Absent septum pellucidum |
| HP:0001339 | Lissencephaly |
| HP:0001460 | Aplasia/Hypoplasia involving the skeletal musculature |
| HP:0002119 | Ventriculomegaly |
| HP:0002126 | Polymicrogyria |
| HP:0002269 | Abnormality of neuronal migration |
| HP:0002334 | Abnormal cerebellar vermis morphology |
| HP:0002536 | Abnormal cortical gyration |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 10329 | RXYLT1 | ribitol xylosyltransferase 1 |
| 10585 | POMT1 | protein O-mannosyltransferase 1 |
| 11041 | B4GAT1 | beta-1,4-glucuronyltransferase 1 |
| 148789 | B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 |
| 1605 | DAG1 | dystroglycan 1 |
| 2218 | FKTN | fukutin |
| 29925 | GMPPB | GDP-mannose pyrophosphorylase B |
| 29954 | POMT2 | protein O-mannosyltransferase 2 |
| 55624 | POMGNT1 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) |
| 729920 | CRPPA | CDP-L-ribitol pyrophosphorylase A |
