Showing entry for Oguchi disease



                               
General Disease Information
BXGD IdBXGD012355
Disease NameOguchi disease
Disease CUI IdC1306122
MeSH Codes C16   C11  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0000478  
Human Phenotype Ontology TermAbnormality of the eye
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease 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
O60840 BXGT004901 Voltage-dependent L-type calcium channel subunit alpha-1F 778 reviewed Ion channel
P08100 BXGT006725 Rhodopsin 6010 reviewed G-protein coupled receptor
Q15835 BXGT013606 Rhodopsin kinase 6011 reviewed Kinase
Q8WTQ7 BXGT018984 Rhodopsin kinase 131890 reviewed Kinase
Q92781 BXGT019372 Retinol dehydrogenase 5 5959 reviewed Enzyme
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