adisease

Showing entry for Hand muscle atrophy

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD004998
Disease Name	Hand muscle atrophy
Disease CUI Id	C0239830
MeSH Codes
Disease Class Name
Semantic Type	Finding
Human Phenotype Ontology Id	HP:0040064 HP:0003011
Human Phenotype Ontology Term	Abnormality of limbs; 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
P08034	BXGT006716	Gap junction beta-1 protein	2705	reviewed	Cell-cell junction
P68133	BXGT011578	Actin, alpha skeletal muscle	58	reviewed	Cellular structure
Q14203	BXGT013455	Dynactin subunit 1	1639	reviewed	Chaperone
Q16595	BXGT013643	Frataxin, mitochondrial	2395	reviewed	Enzyme
Q9HBA0	BXGT020516	Transient receptor potential cation channel subfamily V member 4	59341	reviewed	Ion channel

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}