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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 |
|---|---|---|---|
| 54732 | TMED9 | transmembrane p24 trafficking protein 9 | |
| 55512 | SMPD3 | sphingomyelin phosphodiesterase 3 | |
| 57704 | GBA2 | glucosylceramidase beta 2 | |
| 64083 | GOLPH3 | golgi phosphoprotein 3 | |
| 64116 | SLC39A8 | solute carrier family 39 member 8 | |
| 149175 | MANEAL | mannosidase endo-alpha like | |
| 151056 | PLB1 | phospholipase B1 | |
| 283871 | PGP | phosphoglycolate phosphatase | |
| 284098 | PIGW | phosphatidylinositol glycan anchor biosynthesis class W |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9Y286 | Sialic acid-binding Ig-like lectin 7 |
