adisease

Showing entry for Congenital hypotrichia

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD023750
Disease Name	Congenital hypotrichia
Disease CUI Id	C4721530
MeSH Codes	C16 C17
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0001574
Human Phenotype Ontology Term	Abnormality of the integument
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
P01112	BXGT005732	GTPase HRas	3265	reviewed	Enzyme modulator
P15924	BXGT008171	Desmoplakin	1832	reviewed	Cellular structure
P20936	BXGT008619	Ras GTPase-activating protein 1	5921	reviewed	Enzyme modulator
P22223	BXGT008744	Cadherin-3	1001	reviewed
Q02487	BXGT012656	Desmocollin-2	1824	reviewed	Cell adhesion
Q9Y5Y6	BXGT022308	Suppressor of tumorigenicity 14 protein	6768	reviewed	Enzyme

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}