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autosomal dominant limb-girdle muscular dystrophy type 2
Summary
- Synonym
-
- LGMD1F
- autosomal dominant limb-girdle muscular dystrophy type 1F
- muscular dystrophy limb-girdle type 1F
- Definition
- An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the TNPO3 gene on chromosome 7q32.
- Super Class
- autosomal dominant limb-girdle muscular dystrophy
External Links
- Disease Ontology
- DOID:0110304
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 8972 | MGAM | maltase-glucoamylase | |
| 9104 | RGN | regucalcin | |
| 9200 | HACD1 | 3-hydroxyacyl-CoA dehydratase 1 | |
| 9215 | LARGE1 | LARGE xylosyl- and glucuronyltransferase 1 | |
| 10020 | GNE | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | |
| 10329 | RXYLT1 | ribitol xylosyltransferase 1 | |
| 10585 | POMT1 | protein O-mannosyltransferase 1 | |
| 11041 | B4GAT1 | beta-1,4-glucuronyltransferase 1 | |
| 22933 | SIRT2 | sirtuin 2 | |
| 26033 | ATRNL1 | attractin like 1 |
Related Glycoprotein
