adisease

Showing entry for Usher Syndrome, Type II

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD013420
Disease Name	Usher Syndrome, Type II
Disease CUI Id	C1568249
MeSH Codes	C23 C16 C11 C10 C09
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630 DOID:225
Disease Ontology Class Name	genetic disease; syndrome
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
P24530	BXGT008975	Endothelin receptor type B	1910	reviewed	G-protein coupled receptor
P49019	BXGT010671	Hydroxycarboxylic acid receptor 3	8843	reviewed	G-protein coupled receptor
Q13402	BXGT013348	Unconventional myosin-VIIa	4647	reviewed	Cellular structure
Q96QU1	BXGT019721	Protocadherin-15	65217	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}