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Fukuyama congenital muscular dystrophy
Summary
- Definition
- A congenital muscular dystrophy-dystroglycanopathy type A that is characterized by muscle weakness, failure to thrive, severe intellectual and developmental disability, impaired vision and cardiac abnormalities and has_material_basis_in mutation in the FKTN gene that produces the fukutin protein.
- Super Class
- congenital muscular dystrophy-dystroglycanopathy type A
External Links
- Disease Ontology
- DOID:0050559
- Mondo Disease Ontology
- ORDO
- GARD
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O75072 | Ribitol-5-phosphate transferase FKTN |
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q8R507 | Ribitol-5-phosphate transferase FKTN |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0007260 | Type II lissencephaly |
| HP:0000750 | Delayed speech and language development |
| HP:0100490 | Camptodactyly of finger |
| HP:0007370 | Aplasia/Hypoplasia of the corpus callosum |
| HP:0000767 | Pectus excavatum |
| HP:0000268 | Dolichocephaly |
| HP:0001612 | Weak cry |
| HP:0010864 | Intellectual disability, severe |
| HP:0001371 | Flexion contracture |
| HP:0000007 | Autosomal recessive inheritance |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 2218 | FKTN | fukutin |
| 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 |
| 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 |
