adisease

Showing entry for Hidrotic Ectodermal Dysplasia

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD003940
Disease Name	Hidrotic Ectodermal Dysplasia
Disease CUI Id	C0162361
MeSH Codes	C16 C17
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id	HP:0001574
Human Phenotype Ontology Term	Abnormality of the integument
Disease Ontology Id	DOID:630 DOID:225
Disease Ontology Class Name	genetic disease; syndrome
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
P0DPH7	BXGT007527	Tubulin alpha-3C chain	7278	reviewed
P16144	BXGT008200	Integrin beta-4	3691	reviewed	Receptor
P29033	BXGT009308	Gap junction beta-2 protein	2706	reviewed	Cell-cell junction
P61586	BXGT011375	Transforming protein RhoA	387	reviewed	Enzyme modulator

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}