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
Displaying entries 11 - 20 of 89 in total
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
Displaying all 2 entries
Gene ID Gene Symbol Description Source
98660 Atp1a2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
232975 Atp1a3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
Displaying 1 entry
Gene ID Gene Symbol Description Source
24212 Atp1a2 ATPase Na+/K+ transporting subunit alpha 2

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Acknowledgements

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Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024