adisease

Showing entry for X-linked myopathy with excessive autophagy

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD014390
Disease Name	X-linked myopathy with excessive autophagy
Disease CUI Id	C1839615
MeSH Codes	C16 C05 C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630 DOID:7
Disease Ontology Class Name	genetic disease; 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
P11217	BXGT007674	Glycogen phosphorylase, muscle form	5837	reviewed	Enzyme
P31415	BXGT009537	Calsequestrin-1	844	reviewed
P55072	BXGT011103	Transitional endoplasmic reticulum ATPase	7415	reviewed
P61769	BXGT011383	Beta-2-microglobulin	567	reviewed	Immune response
P68133	BXGT011578	Actin, alpha skeletal muscle	58	reviewed	Cellular structure
Q13501	BXGT013365	Sequestosome-1	8878	reviewed
Q9Y223	BXGT022207	Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	10020	reviewed	Enzyme

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}