Showing entry for Congenital Fibrosis of the Extraocular Muscles



                               
General Disease Information
BXGD IdBXGD012316
Disease NameCongenital Fibrosis of the Extraocular Muscles
Disease CUI IdC1302995
MeSH Codes C23   C11   C10  
Disease Class NamePathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0000152   HP:0003011  
Human Phenotype Ontology TermAbnormality of head or neck; Abnormality of the musculature
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
P21817 BXGT008693 Ryanodine receptor 1 6261 reviewed Ion channel
P46821 BXGT010542 Microtubule-associated protein 1B 4131 reviewed Cellular structure
Q13509 BXGT013366 Tubulin beta-3 chain 10381 reviewed Cellular structure
Q9BVA1 BXGT020142 Tubulin beta-2B chain 347733 reviewed
Q7Z4S6 BXGT023001 Kinesin-like protein KIF21A 55605 reviewed Cellular structure
Q14678 BXGT023543 KN motif and ankyrin repeat domain-containing protein 1 23189 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