adisease

Showing entry for Folate Malabsorption, Hereditary

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD007531
Disease Name	Folate Malabsorption, Hereditary
Disease CUI Id	C0342705
MeSH Codes	C06 C18
Disease Class Name	Digestive System Diseases; 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
P14207	BXGT007993	Folate receptor beta	2350	reviewed
P15328	BXGT008108	Folate receptor alpha	2348	reviewed
Q6SZW1	BXGT025034	NAD(+) hydrolase SARM1	23098	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}