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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 |
|---|---|---|---|
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 2990 | GUSB | glucuronidase beta | |
| 3098 | HK1 | hexokinase 1 | |
| 3251 | HPRT1 | hypoxanthine phosphoribosyltransferase 1 | |
| 3419 | IDH3A | isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha | |
| 3423 | IDS | iduronate 2-sulfatase | |
| 3636 | INPPL1 | inositol polyphosphate phosphatase like 1 | |
| 3897 | L1CAM | L1 cell adhesion molecule | |
| 4069 | LYZ | lysozyme | |
| 4099 | MAG | myelin associated glycoprotein |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9Y286 | Sialic acid-binding Ig-like lectin 7 |
