adisease

Showing entry for Greig cephalopolysyndactyly syndrome

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD005509
Disease Name	Greig cephalopolysyndactyly syndrome
Disease CUI Id	C0265306
MeSH Codes	C16 C05
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630 DOID:7 DOID:150
Disease Ontology Class Name	genetic disease; disease of anatomical entity; disease of mental health
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
P00533	BXGT005575	Epidermal growth factor receptor	1956	reviewed	Kinase
P01133	BXGT005736	Pro-epidermal growth factor	1950	reviewed
P05231	BXGT006345	Interleukin-6	3569	reviewed
P08151	BXGT006731	Zinc finger protein GLI1	2735	reviewed
P32754	BXGT009664	4-hydroxyphenylpyruvate dioxygenase	3242	reviewed	Enzyme
P35557	BXGT009846	Glucokinase	2645	reviewed	Kinase
Q9UKV8	BXGT021752	Protein argonaute-2	27161	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}