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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 |
|---|---|---|---|
| 28 | ABO | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | |
| 43 | ACHE | acetylcholinesterase (Yt blood group) | |
| 142 | PARP1 | poly(ADP-ribose) polymerase 1 | |
| 224 | ALDH3A2 | aldehyde dehydrogenase 3 family member A2 | |
| 410 | ARSA | arylsulfatase A | |
| 477 | ATP1A2 | ATPase Na+/K+ transporting subunit alpha 2 | |
| 684 | BST2 | bone marrow stromal cell antigen 2 | |
| 912 | CD1D | CD1d molecule | |
| 1012 | CDH13 | cadherin 13 | |
| 1116 | CHI3L1 | chitinase 3 like 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9Y286 | Sialic acid-binding Ig-like lectin 7 |
