adisease

Showing entry for Abnormality of the helix

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD015629
Disease Name	Abnormality of the helix
Disease CUI Id	C1856660
MeSH Codes
Disease Class Name
Semantic Type	Finding
Human Phenotype Ontology Id	HP:0000598
Human Phenotype Ontology Term	Abnormality of the ear
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
O00204	BXGT003893	Sulfotransferase family cytosolic 2B member 1	6820	reviewed
P21359	BXGT008640	Neurofibromin	4763	reviewed	Enzyme modulator
P22607	BXGT008784	Fibroblast growth factor receptor 3	2261	reviewed	Kinase
P36507	BXGT009923	Dual specificity mitogen-activated protein kinase kinase 2	5605	reviewed	Kinase
P50542	BXGT010808	Peroxisomal targeting signal 1 receptor	5830	reviewed	Transporter
Q00604	BXGT012538	Norrin	4693	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}