Showing entry for Eye Diseases, Hereditary



                               
General Disease Information
BXGD IdBXGD000984
Disease NameEye Diseases, Hereditary
Disease CUI IdC0015398
MeSH Codes C16   C11  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
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
O00444 BXGT003921 Serine/threonine-protein kinase PLK4 10733 reviewed Kinase
O60313 BXGT004871 Dynamin-like 120 kDa protein, mitochondrial 4976 reviewed Enzyme modulator
O95237 BXGT005361 Lecithin retinol acyltransferase 9227 reviewed
P11308 BXGT007684 Transcriptional regulator ERG 2078 reviewed Transcription factor
P12271 BXGT007786 Retinaldehyde-binding protein 1 6017 reviewed Transporter
P98164 BXGT012230 Low-density lipoprotein receptor-related protein 2 4036 reviewed
Q92781 BXGT019372 Retinol dehydrogenase 5 5959 reviewed Enzyme
Q9NRR6 BXGT021193 Phosphatidylinositol polyphosphate 5-phosphatase type IV 56623 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