adisease

Showing entry for Constitutional Mismatch Repair Deficiency Syndrome

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD022747
Disease Name	Constitutional Mismatch Repair Deficiency Syndrome
Disease CUI Id	C4321324
MeSH Codes	C16 C04
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
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
P22897	BXGT008816	Macrophage mannose receptor 1	4360	reviewed
P35222	BXGT009799	Catenin beta-1	1499	reviewed
P40692	BXGT010195	DNA mismatch repair protein Mlh1	4292	reviewed	Nucleic acid binding
P43246	BXGT010371	DNA mismatch repair protein Msh2	4436	reviewed	Nucleic acid binding
P52701	BXGT010943	DNA mismatch repair protein Msh6	2956	reviewed	Nucleic acid binding
P54278	BXGT011038	Mismatch repair endonuclease PMS2	5395	reviewed	Nucleic acid binding

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}