adisease

Showing entry for Gallbladder anomaly congenital

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD005635
Disease Name	Gallbladder anomaly congenital
Disease CUI Id	C0266249
MeSH Codes	C16 C06
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0025031
Human Phenotype Ontology Term	Abnormality of the digestive system
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
O96028	BXGT005417	Histone-lysine N-methyltransferase NSD2	7468	reviewed	Epigenetic regulator
P00747	BXGT005639	Plasminogen	5340	reviewed	Enzyme
P04066	BXGT006142	Tissue alpha-L-fucosidase	2517	reviewed
Q15831	BXGT013604	Serine/threonine-protein kinase STK11	6794	reviewed	Kinase
Q9UBM7	BXGT021657	7-dehydrocholesterol reductase	1717	reviewed	Enzyme

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}