adisease

Showing entry for Limb-girdle muscular dystrophy type 2H

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD006143
Disease Name	Limb-girdle muscular dystrophy type 2H
Disease CUI Id	C0270968
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; Congenital Abnormality
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
O75129	BXGT005101	Astrotactin-2	23245	reviewed
P01375	BXGT005753	Tumor necrosis factor	7124	reviewed	Signaling
P61086	BXGT011357	Ubiquitin-conjugating enzyme E2 K	3093	reviewed
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}