adisease

Showing entry for Dentinogenesis imperfecta - Shield's type III (disorder)

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD008242
Disease Name	Dentinogenesis imperfecta - Shield's type III (disorder)
Disease CUI Id	C0399378
MeSH Codes	C16 C07
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:7
Disease Ontology Class Name	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
P52895	BXGT010961	Aldo-keto reductase family 1 member C2	1646	reviewed	Enzyme
Q04828	BXGT012787	Aldo-keto reductase family 1 member C1	1645	reviewed	Enzyme

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}