adisease

Showing entry for Hyperbilirubinemia, Hereditary

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD001380
Disease Name	Hyperbilirubinemia, Hereditary
Disease CUI Id	C0020435
MeSH Codes	C16 C18
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:0014667 DOID:630
Disease Ontology Class Name	disease of metabolism; genetic disease
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
O15438	BXGT004168	Canalicular multispecific organic anion transporter 2	8714	reviewed	Transporter
P05937	BXGT006396	Calbindin	793	reviewed	Calcium-binding protein
P08397	BXGT006768	Porphobilinogen deaminase	3145	reviewed	Enzyme
P08709	BXGT006818	Coagulation factor VII	2155	reviewed	Enzyme
P09429	BXGT006889	High mobility group protein B1	3146	reviewed	Nucleic acid binding
P10415	BXGT007567	Apoptosis regulator Bcl-2	596	reviewed	Signaling
P22557	BXGT008783	5-aminolevulinate synthase, erythroid-specific, mitochondrial	212	reviewed	Enzyme
Q92887	BXGT019389	Canalicular multispecific organic anion transporter 1	1244	reviewed	Transporter

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}