adisease

Showing entry for Generalized hypopigmentation

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD015088
Disease Name	Generalized hypopigmentation
Disease CUI Id	C1849923
MeSH Codes	C17
Disease Class Name	Skin and Connective Tissue Diseases
Semantic Type	Finding
Human Phenotype Ontology Id	HP:0001574
Human Phenotype Ontology Term	Abnormality of the integument
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
O75030	BXGT005096	Microphthalmia-associated transcription factor	4286	reviewed
P00439	BXGT005539	Phenylalanine-4-hydroxylase	5053	reviewed
Q01968	BXGT012626	Inositol polyphosphate 5-phosphatase OCRL-1	4952	reviewed	Enzyme
Q86YC2	BXGT017633	Partner and localizer of BRCA2	79728	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}