adisease

Showing entry for Alport Syndrome, X-Linked

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD013415
Disease Name	Alport Syndrome, X-Linked
Disease CUI Id	C1567742
MeSH Codes	C16 C13 C17 C12
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630
Disease Ontology Class Name	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
P00797	BXGT005658	Renin	5972	reviewed	Enzyme
P02649	BXGT005909	Apolipoprotein E	348	reviewed
P08603	BXGT006798	Complement factor H	3075	reviewed
P27169	BXGT009161	Serum paraoxonase/arylesterase 1	5444	reviewed
P29400	BXGT009343	Collagen alpha-5(IV) chain	1287	reviewed
P35579	BXGT009852	Myosin-9	4627	reviewed
P42898	BXGT010344	Methylenetetrahydrofolate reductase	4524	reviewed
Q01955	BXGT023255	Collagen alpha-3(IV) chain	1285	reviewed

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}