Showing entry for Hypoplasia of iris



                               
General Disease Information
BXGD IdBXGD007690
Disease NameHypoplasia of iris
Disease CUI IdC0344539
MeSH Codes C11  
Disease Class NameEye Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id HP:0000478  
Human Phenotype Ontology TermAbnormality of the eye
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
P11362 BXGT007693 Fibroblast growth factor receptor 1 2260 reviewed Kinase
P27986 BXGT009216 Phosphatidylinositol 3-kinase regulatory subunit alpha 5295 reviewed Kinase
P35555 BXGT009845 Fibrillin-1 2200 reviewed Calcium-binding protein
Q00604 BXGT012538 Norrin 4693 reviewed
Q03468 BXGT012716 DNA excision repair protein ERCC-6 2074 reviewed
Q13586 BXGT013380 Stromal interaction molecule 1 6786 reviewed
Q14643 BXGT013493 Inositol 1,4,5-trisphosphate receptor type 1 3708 reviewed Ion channel
Q59FF6 BXGT023693 Excision repair cross-complementing rodent repair deficiency, complementation group 6 variant 2074 unreviewed
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