adisease

Showing entry for Infantile axial hypotonia

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD019520
Disease Name	Infantile axial hypotonia
Disease CUI Id	C3806604
MeSH Codes
Disease Class Name
Semantic Type	Finding
Human Phenotype Ontology Id	HP:0003011
Human Phenotype Ontology Term	Abnormality of the musculature
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations

The disease-related target proteins

Proteins

Uniport Id	BXGT Id	Protein Name	Gene	Status	Protein Class
Uniport Id	BXGT Id	Protein name	Gene	Status	Protein class
P17900	BXGT008353	Ganglioside GM2 activator	2760	reviewed	Transporter
P21817	BXGT008693	Ryanodine receptor 1	6261	reviewed	Ion channel
P22607	BXGT008784	Fibroblast growth factor receptor 3	2261	reviewed	Kinase
P54136	BXGT011033	Arginine--tRNA ligase, cytoplasmic	5917	reviewed
P55789	BXGT011126	FAD-linked sulfhydryl oxidase ALR	2671	reviewed	Enzyme
Q12879	BXGT013275	Glutamate receptor ionotropic, NMDA 2A	2903	reviewed	Ion channel
Q13509	BXGT013366	Tubulin beta-3 chain	10381	reviewed	Cellular structure
Q9UQD0	BXGT021811	Sodium channel protein type 8 subunit alpha	6334	reviewed	Ion channel
Q9Y617	BXGT022314	Phosphoserine aminotransferase	29968	reviewed

The disease-related compounds

Compounds

BXGC Id	Compound Name	Structure	Molecular Weight	Number of targets^{?Number of times compound connecting the disease , higher numbers indicate the compound is more associated with the disease}

The disease-related foods

Foods

BXGF Id	Food Name	Scientific Name	Food Group	Number of compounds in food^{?Number of compounds in food that connecting disease, higher numbers indicate the more compounds in food are more associated with the dusease}