adisease

Showing entry for Hereditary systemic amyloidosis

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD022080
Disease Name	Hereditary systemic amyloidosis
Disease CUI Id	C4081731
MeSH Codes	C16 C18
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
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
P02647	BXGT005908	Apolipoprotein A-I	335	reviewed
P02656	BXGT005913	Apolipoprotein C-III	345	reviewed
P02671	BXGT005914	Fibrinogen alpha chain	2243	reviewed
P02766	BXGT005953	Transthyretin	7276	reviewed	Transporter
P61626	BXGT011382	Lysozyme C	4069	reviewed
P61769	BXGT011383	Beta-2-microglobulin	567	reviewed	Immune response
Q96P20	BXGT019704	NACHT, LRR and PYD domains-containing protein 3	114548	reviewed
Q9NPI8	BXGT021161	Fanconi anemia group F protein	2188	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}