GlyCosmos Portal

alternating hemiplegia of childhood

Synonym

Definition

A hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body.

Super Class

hemiplegia

Disease Ontology

DOID:0050635

Mondo Disease Ontology

MeSH

ORDO

OMIM

GARD

MGI genotype (from TogoID)

Related Genes

Displaying entries **81 - 89** of 89 in total

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Gene ID	Gene Symbol	Description	Source
54732	TMED9	transmembrane p24 trafficking protein 9	DisGeNET
55512	SMPD3	sphingomyelin phosphodiesterase 3	DisGeNET
57704	GBA2	glucosylceramidase beta 2	DisGeNET
64083	GOLPH3	golgi phosphoprotein 3	DisGeNET
64116	SLC39A8	solute carrier family 39 member 8	DisGeNET
149175	MANEAL	mannosidase endo-alpha like	DisGeNET
151056	PLB1	phospholipase B1	DisGeNET
283871	PGP	phosphoglycolate phosphatase	DisGeNET
284098	PIGW	phosphatidylinositol glycan anchor biosynthesis class W	DisGeNET

Displaying **all 2** entries
Gene ID	Gene Symbol	Description	Source
98660	Atp1a2	ATPase, Na+/K+ transporting, alpha 2 polypeptide	Alliance of Genome Resources
232975	Atp1a3	ATPase, Na+/K+ transporting, alpha 3 polypeptide	Alliance of Genome Resources

Displaying 1 entry
Gene ID	Gene Symbol	Description	Source
24212	Atp1a2	ATPase Na+/K+ transporting subunit alpha 2	Alliance of Genome Resources

Related Glycoprotein

Displaying entries **1 - 10** of 71 in total

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UniProt ID	Protein Name	Source
A6NDG6	Glycerol-3-phosphate phosphatase	DisGeNET
O00329	Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform	DisGeNET
O00462	Beta-mannosidase	DisGeNET
O14594	Neurocan core protein	DisGeNET
O15121	Sphingolipid delta(4)-desaturase DES1	DisGeNET
O15357	Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2	DisGeNET
O15496	Group 10 secretory phospholipase A2	DisGeNET
O60502	Protein O-GlcNAcase	DisGeNET
O60760	Hematopoietic prostaglandin D synthase	DisGeNET
O75326	Semaphorin-7A	DisGeNET