Showing entry for Arrhythmogenic Right Ventricular Dysplasia, Familial, 9



                               
General Disease Information
BXGD IdBXGD014177
Disease NameArrhythmogenic Right Ventricular Dysplasia, Familial, 9
Disease CUI IdC1836906
MeSH Codes C16   C14  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic 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
P02545 BXGT005889 Prelamin-A/C 4000 reviewed
P15924 BXGT008171 Desmoplakin 1832 reviewed Cellular structure
Q99959 BXGT019977 Plakophilin-2 5318 reviewed Cellular structure
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