adisease

Showing entry for Hypomineralization of enamel of tooth

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD019296
Disease Name	Hypomineralization of enamel of tooth
Disease CUI Id	C3665628
MeSH Codes	C16 C07
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id	HP:0000152 HP:0000924 HP:0003549
Human Phenotype Ontology Term	Abnormality of head or neck; Abnormality of the skeletal system; Abnormality of connective tissue
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
P35222	BXGT009799	Catenin beta-1	1499	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}