adisease

Showing entry for ICHTHYOSIS PREMATURITY SYNDROME

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD014251
Disease Name	ICHTHYOSIS PREMATURITY SYNDROME
Disease CUI Id	C1837610
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
Human Phenotype Ontology Term
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
O00522	BXGT003935	Krev interaction trapped protein 1	889	reviewed
P0DP23	BXGT007520	Calmodulin-1	808	reviewed
P0DP24	BXGT007521	Calmodulin-2	808	reviewed
P27708	BXGT009202	CAD protein	790	reviewed	Enzyme
Q9NPH2	BXGT021158	Inositol-3-phosphate synthase 1	51477	reviewed
Q7Z624	BXGT022792	Calmodulin-lysine N-methyltransferase	79823	reviewed
P0DP25	BXGT024595	Calmodulin-3	808	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}