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alternating hemiplegia of childhood
Summary
- Synonym
-
- AHC
- Definition
- A hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body.
- Super Class
- hemiplegia
External Links
- Disease Ontology
- DOID:0050635
- Mondo Disease Ontology
- MeSH
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1738 | DLD | dihydrolipoamide dehydrogenase | |
| 2026 | ENO2 | enolase 2 | |
| 2220 | FCN2 | ficolin 2 | |
| 2571 | GAD1 | glutamate decarboxylase 1 | |
| 2572 | GAD2 | glutamate decarboxylase 2 | |
| 2583 | B4GALNT1 | beta-1,4-N-acetyl-galactosaminyltransferase 1 | |
| 2629 | GBA1 | glucosylceramidase beta 1 | |
| 2639 | GCDH | glutaryl-CoA dehydrogenase | |
| 2752 | GLUL | glutamate-ammonia ligase | |
| 2821 | GPI | glucose-6-phosphate isomerase |
Related Glycoprotein
