adisease

Showing entry for MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD015185
Disease Name	MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
Disease CUI Id	C1850889
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
P01019	BXGT005717	Angiotensinogen	183	reviewed	Enzyme modulator
P08758	BXGT006821	Annexin A5	308	reviewed
P11473	BXGT007709	Vitamin D3 receptor	7421	reviewed	Nuclear receptor
P20807	BXGT008601	Calpain-3	825	reviewed	Enzyme
P55087	BXGT011105	Aquaporin-4	361	reviewed	Ion channel
Q07837	BXGT012943	Neutral and basic amino acid transport protein rBAT	6519	reviewed	Transporter
Q14203	BXGT013455	Dynactin subunit 1	1639	reviewed	Chaperone
Q9NZM1	BXGT023948	Myoferlin	26509	reviewed	Transporter

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}