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autosomal recessive limb-girdle muscular dystrophy type 2M
Summary
- Synonym
-
- LGMD2M
- MDDGC4
- muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4
- Definition
- An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding fukutin (FKTN) on chromosome 9q31.
- Super Class
- autosomal recessive limb-girdle muscular dystrophy
External Links
- Disease Ontology
- DOID:0110296
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1120 | CHKB | choline kinase beta | |
| 1497 | CTNS | cystinosin, lysosomal cystine transporter | |
| 1605 | DAG1 | dystroglycan 1 | |
| 1634 | DCN | decorin | |
| 1636 | ACE | angiotensin I converting enzyme | |
| 1800 | DPEP1 | dipeptidase 1 | |
| 2023 | ENO1 | enolase 1 | |
| 2218 | FKTN | fukutin | |
| 2548 | GAA | alpha glucosidase | |
| 2710 | GK | glycerol kinase |
Related Glycoprotein
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0003560 | Muscular dystrophy |
| HP:0001270 | Motor delay |
| HP:0003712 | Skeletal muscle hypertrophy |
| HP:0003236 | Elevated circulating creatine kinase concentration |
| HP:0009060 | Scapular muscle atrophy |
| HP:0001762 | Talipes equinovarus |
| HP:0003676 | Progressive |
| HP:0001252 | Hypotonia |
| HP:0003323 | Progressive muscle weakness |
