adisease

Showing entry for Keratoderma, Palmoplantar, Epidermolytic

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD013700
Disease Name	Keratoderma, Palmoplantar, Epidermolytic
Disease CUI Id	C1721006
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: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
P03952	BXGT006118	Plasma kallikrein	3818	reviewed	Enzyme
P04264	BXGT006176	Keratin, type II cytoskeletal 1	3848	reviewed
P08779	BXGT006824	Keratin, type I cytoskeletal 16	3868	reviewed
P29033	BXGT009308	Gap junction beta-2 protein	2706	reviewed	Cell-cell junction
P35527	BXGT009843	Keratin, type I cytoskeletal 9	3857	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}