adisease

Showing entry for Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD023443
Disease Name	Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1
Disease CUI Id	C4551951
MeSH Codes	C16 C18 C05 C10 F03
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630 DOID:225
Disease Ontology Class Name	genetic disease; syndrome
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
P55072	BXGT011103	Transitional endoplasmic reticulum ATPase	7415	reviewed
P78344	BXGT011835	Eukaryotic translation initiation factor 4 gamma 2	1982	reviewed	Nucleic acid binding
Q04912	BXGT012790	Macrophage-stimulating protein receptor	4486	reviewed	Kinase

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}