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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 |
|---|---|---|---|
| 4126 | MANBA | mannosidase beta | |
| 4668 | NAGA | alpha-N-acetylgalactosaminidase | |
| 4684 | NCAM1 | neural cell adhesion molecule 1 | |
| 4860 | PNP | purine nucleoside phosphorylase | |
| 4967 | OGDH | oxoglutarate dehydrogenase | |
| 5048 | PAFAH1B1 | platelet activating factor acetylhydrolase 1b regulatory subunit 1 | |
| 5168 | ENPP2 | ectonucleotide pyrophosphatase/phosphodiesterase 2 | |
| 5290 | PIK3CA | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | |
| 5291 | PIK3CB | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta | |
| 5293 | PIK3CD | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P17050 | Alpha-N-acetylgalactosaminidase | |
| P17405 | Sphingomyelin phosphodiesterase | |
| P19367 | Hexokinase-1 | |
| P20916 | Myelin-associated glycoprotein | |
| P21964 | Catechol O-methyltransferase | |
| P22303 | Acetylcholinesterase | |
| P22304 | Iduronate 2-sulfatase | |
| P32004 | Neural cell adhesion molecule L1 | |
| P35354 | Prostaglandin G/H synthase 2 | |
| P36222 | Chitinase-3-like protein 1 |
