Showing entry for Hereditary bundle branch system defect



                               
General Disease Information
BXGD IdBXGD016570
Disease NameHereditary bundle branch system defect
Disease CUI IdC1879286
MeSH Codes C23   C14  
Disease Class NamePathological Conditions, Signs and Symptoms; 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
P15924 BXGT008171 Desmoplakin 1832 reviewed Cellular structure
P52952 BXGT010966 Homeobox protein Nkx-2.5 1482 reviewed Transcription factor
Q14524 BXGT013478 Sodium channel protein type 5 subunit alpha 6331 reviewed Ion channel
Q8TD43 BXGT018806 Transient receptor potential cation channel subfamily M member 4 54795 reviewed Ion channel
Q96RP8 BXGT019731 Potassium voltage-gated channel subfamily A member 7 3743 reviewed Ion channel
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