adisease

Showing entry for Congenital absence of vas deferens

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD005669
Disease Name	Congenital absence of vas deferens
Disease CUI Id	C0266444
MeSH Codes
Disease Class Name
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000119
Human Phenotype Ontology Term	Abnormality of the genitourinary 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
P08183	BXGT006741	ATP-dependent translocase ABCB1	5243	reviewed	Transporter
P10275	BXGT007552	Androgen receptor	367	reviewed	Nuclear receptor
P13569	BXGT007923	Cystic fibrosis transmembrane conductance regulator	1080	reviewed	Ion channel
P33527	BXGT009728	Multidrug resistance-associated protein 1	4363	reviewed	Transporter
P41235	BXGT010241	Hepatocyte nuclear factor 4-alpha	3172	reviewed	Nuclear receptor

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}