adisease

Showing entry for Aplasia of muscle

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD008730
Disease Name	Aplasia of muscle
Disease CUI Id	C0432185
MeSH Codes	C16
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic Type	Congenital Abnormality
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
O95180	BXGT005358	Voltage-dependent T-type calcium channel subunit alpha-1H	8912	reviewed	Ion channel
P02708	BXGT005927	Acetylcholine receptor subunit alpha	1134	reviewed	Ion channel
P07510	BXGT006631	Acetylcholine receptor subunit gamma	1146	reviewed	Ion channel
P11217	BXGT007674	Glycogen phosphorylase, muscle form	5837	reviewed	Enzyme
Q07001	BXGT012907	Acetylcholine receptor subunit delta	1144	reviewed	Ion channel
Q9HBA0	BXGT020516	Transient receptor potential cation channel subfamily V member 4	59341	reviewed	Ion channel
Q9NY65	BXGT021252	Tubulin alpha-8 chain	51807	reviewed	Cellular structure
O43148	BXGT023017	mRNA cap guanine-N7 methyltransferase	8731	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}