adisease

Showing entry for Night Blindness, Congenital Stationary, Type 1A

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD018996
Disease Name	Night Blindness, Congenital Stationary, Type 1A
Disease CUI Id	C3495587
MeSH Codes	C16 C11
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; 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
O15303	BXGT004150	Metabotropic glutamate receptor 6	2916	reviewed	G-protein coupled receptor
O60840	BXGT004901	Voltage-dependent L-type calcium channel subunit alpha-1F	778	reviewed	Ion channel
P08100	BXGT006725	Rhodopsin	6010	reviewed	G-protein coupled receptor
P11488	BXGT007713	Guanine nucleotide-binding protein G(t) subunit alpha-1	2779	reviewed	Enzyme modulator
P35913	BXGT009879	Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta	5158	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}