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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 |
|---|---|---|---|
| 10558 | SPTLC1 | serine palmitoyltransferase long chain base subunit 1 | |
| 10724 | OGA | O-GlcNAcase | |
| 10825 | NEU3 | neuraminidase 3 | |
| 10908 | PNPLA6 | patatin like phospholipase domain containing 6 | |
| 11343 | MGLL | monoglyceride lipase | |
| 22933 | SIRT2 | sirtuin 2 | |
| 23098 | SARM1 | sterile alpha and TIR motif containing 1 | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 27036 | SIGLEC7 | sialic acid binding Ig like lectin 7 | |
| 27306 | HPGDS | hematopoietic prostaglandin D synthase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9Y286 | Sialic acid-binding Ig-like lectin 7 |
