adisease

Showing entry for Cap Myopathy

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD019375
Disease Name	Cap Myopathy
Disease CUI Id	C3710589
MeSH Codes	C05 C10
Disease Class Name	Musculoskeletal Diseases; Nervous System Diseases
Semantic Type	Disease or Syndrome; Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
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
P06753	BXGT006498	Tropomyosin alpha-3 chain	7170	reviewed	Cellular structure
P09493	BXGT006900	Tropomyosin alpha-1 chain	7168	reviewed	Cellular structure
P60709	BXGT011322	Actin, cytoplasmic 1	60	reviewed	Cellular structure
P68133	BXGT011578	Actin, alpha skeletal muscle	58	reviewed	Cellular structure

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}