adisease

Showing entry for Cardiomyopathy, Familial Hypertrophic, 1 (disorder)

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD018989
Disease Name	Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Disease CUI Id	C3495498
MeSH Codes	C16 C14
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:7
Disease Ontology Class Name	disease of anatomical entity
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
P45379	BXGT010459	Troponin T, cardiac muscle	7139	reviewed	Cellular structure
Q13936	BXGT013404	Voltage-dependent L-type calcium channel subunit alpha-1C	775	reviewed	Ion channel
Q9H1R3	BXGT020446	Myosin light chain kinase 2, skeletal/cardiac muscle	85366	reviewed	Kinase

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}