adisease

Showing entry for Congenital absence of part of brain

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD005673
Disease Name	Congenital absence of part of brain
Disease CUI Id	C0266461
MeSH Codes	C16
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630 DOID:7 DOID:225 DOID:150 DOID:0080015
Disease Ontology Class Name	genetic disease; disease of anatomical entity; syndrome; disease of mental health; physical disorder
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
Q9BVA1	BXGT020142	Tubulin beta-2B chain	347733	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}