adisease

Showing entry for Amelogenesis Imperfecta hypomaturation type

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD008240
Disease Name	Amelogenesis Imperfecta hypomaturation type
Disease CUI Id	C0399372
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
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
O60882	BXGT004905	Matrix metalloproteinase-20	9313	reviewed	Enzyme
Q9Y5K2	BXGT022293	Kallikrein-4	9622	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}