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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 |
|---|---|---|---|
| 6785 | ELOVL4 | ELOVL fatty acid elongase 4 | |
| 7167 | TPI1 | triosephosphate isomerase 1 | |
| 7903 | ST8SIA4 | ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4 | |
| 8398 | PLA2G6 | phospholipase A2 group VI | |
| 8399 | PLA2G10 | phospholipase A2 group X | |
| 8482 | SEMA7A | semaphorin 7A (JohnMiltonHagen blood group) | |
| 8560 | DEGS1 | delta 4-desaturase, sphingolipid 1 | |
| 8803 | SUCLA2 | succinate-CoA ligase ADP-forming subunit beta | |
| 9254 | CACNA2D2 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | |
| 9365 | KL | klotho |
Related Glycoprotein
