Showing entry for Amyloidosis, familial visceral



                               
General Disease Information
BXGD IdBXGD005928
Disease NameAmyloidosis, familial visceral
Disease CUI IdC0268389
MeSH Codes C16   C18  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:0014667  
Disease Ontology Class Namedisease of metabolism
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
P02647 BXGT005908 Apolipoprotein A-I 335 reviewed
P02671 BXGT005914 Fibrinogen alpha chain 2243 reviewed
P06396 BXGT006435 Gelsolin 2934 reviewed Cellular structure
P08575 BXGT006793 Receptor-type tyrosine-protein phosphatase C 5788 reviewed Enzyme
P28907 BXGT009301 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 952 reviewed Enzyme
P61626 BXGT011382 Lysozyme C 4069 reviewed
P61769 BXGT011383 Beta-2-microglobulin 567 reviewed Immune response
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