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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 |
|---|---|---|---|
| 1298 | COL9A2 | collagen type IX alpha 2 chain | |
| 1312 | COMT | catechol-O-methyltransferase | |
| 1463 | NCAN | neurocan | |
| 1544 | CYP1A2 | cytochrome P450 family 1 subfamily A member 2 | |
| 1555 | CYP2B6 | cytochrome P450 family 2 subfamily B member 6 | |
| 1558 | CYP2C8 | cytochrome P450 family 2 subfamily C member 8 | |
| 1559 | CYP2C9 | cytochrome P450 family 2 subfamily C member 9 | |
| 1593 | CYP27A1 | cytochrome P450 family 27 subfamily A member 1 | |
| 1636 | ACE | angiotensin I converting enzyme | |
| 1727 | CYB5R3 | cytochrome b5 reductase 3 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9Y286 | Sialic acid-binding Ig-like lectin 7 |
