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congenital muscular dystrophy-dystroglycanopathy type A6
Summary
- Synonym
-
- MDDGA6
- Walker-Warburg syndrome or muscle-eye-brain disease, LARGE-related
- congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A6
- Definition
- A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in LARGE on 22q12.3.
- Super Class
- congenital muscular dystrophy-dystroglycanopathy type A
External Links
- Disease Ontology
- DOID:0111242
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source | Organism |
|---|---|---|---|---|
| 100498555 | large1 | LARGE xylosyl- and glucuronyltransferase 1 | Xenopus tropicalis (tropical clawed frog) | |
| 108704366 | large1.L | LARGE xylosyl- and glucuronyltransferase 1 L homeolog | Xenopus laevis (African clawed frog) | |
| 108712551 | large1.S | LARGE xylosyl- and glucuronyltransferase 1 S homeolog | Xenopus laevis (African clawed frog) |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003457 | EMG abnormality |
| HP:0004374 | Hemiplegia/hemiparesis |
| HP:0007360 | Aplasia/Hypoplasia of the cerebellum |
| HP:0100022 | Abnormality of movement |
| HP:0100543 | Cognitive impairment |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000519 | Developmental cataract |
| HP:0000580 | Pigmentary retinopathy |
| HP:0001290 | Generalized hypotonia |
| HP:0001371 | Flexion contracture |
