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autosomal recessive limb-girdle muscular dystrophy type 2P
Summary
- Synonym
-
- LGMD2P
- MDDGC9
- muscular dystrophy-dystroglycanopathy (limb-girdle) type C9
- muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related
- Definition
- An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gene encoding alpha-dystroglycan (DAG1) on chromosome 3p21.
- Super Class
- autosomal recessive limb-girdle muscular dystrophy
External Links
- Disease Ontology
- DOID:0110293
- Mondo Disease Ontology
- ORDO
- OMIM
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 84892 | POMGNT2 | protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) | |
| 120071 | LARGE2 | LARGE xylosyl- and glucuronyltransferase 2 | |
| 124872 | B4GALNT2 | beta-1,4-N-acetyl-galactosaminyltransferase 2 (SID blood group) | |
| 148789 | B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 | |
| 729920 | CRPPA | CDP-L-ribitol pyrophosphorylase A |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002317 | Unsteady gait |
| HP:0008981 | Calf muscle hypertrophy |
| HP:0002515 | Waddling gait |
| HP:0003551 | Difficulty climbing stairs |
| HP:0001263 | Global developmental delay |
| HP:0003560 | Muscular dystrophy |
| HP:0000750 | Delayed speech and language development |
| HP:0011463 | Childhood onset |
| HP:0002355 | Difficulty walking |
| HP:0000007 | Autosomal recessive inheritance |
