adisease

Showing entry for LEBER CONGENITAL AMAUROSIS 12 (disorder)

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD015745
Disease Name	LEBER CONGENITAL AMAUROSIS 12 (disorder)
Disease CUI Id	C1857743
MeSH Codes	C11
Disease Class Name	Eye Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630 DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
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
Q15835	BXGT013606	Rhodopsin kinase	6011	reviewed	Kinase
Q8WTQ7	BXGT018984	Rhodopsin kinase	131890	reviewed	Kinase

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}