adisease

Showing entry for CONOTRUNCAL ANOMALY FACE SYNDROME

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD010762
Disease Name	CONOTRUNCAL ANOMALY FACE SYNDROME
Disease CUI Id	C0795907
MeSH Codes	C16 C05 C19 C15 C14
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
Semantic Type	Disease or Syndrome
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
P10145	BXGT007542	Interleukin-8	3576	reviewed	Signaling
P13224	BXGT007890	Platelet glycoprotein Ib beta chain	2812	reviewed
P21964	BXGT008714	Catechol O-methyltransferase	1312	reviewed	Enzyme
Q15652	BXGT013587	Probable JmjC domain-containing histone demethylation protein 2C	221037	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}