adisease

Showing entry for Limb-girdle muscular dystrophy type 2A

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD016553
Disease Name	Limb-girdle muscular dystrophy type 2A
Disease CUI Id	C1869123
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: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
O75923	BXGT005166	Dysferlin	8291	reviewed	Transporter
P15056	BXGT008075	Serine/threonine-protein kinase B-raf	673	reviewed	Kinase
P20807	BXGT008601	Calpain-3	825	reviewed	Enzyme
P35222	BXGT009799	Catenin beta-1	1499	reviewed
P60709	BXGT011322	Actin, cytoplasmic 1	60	reviewed	Cellular structure
Q14315	BXGT013460	Filamin-C	2318	reviewed
Q15149	BXGT013547	Plectin	5339	reviewed	Cellular structure
Q8WZ42	BXGT019023	Titin	7273	reviewed	Kinase
Q9H9S5	BXGT024623	Fukutin-related protein	79147	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}