adisease

Showing entry for Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD008409
Disease Name	Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
Disease CUI Id	C0410173
MeSH Codes	C16 C05 C08 C10 C14
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Respiratory Tract Diseases; Nervous System Diseases; Cardiovascular 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
P04637	BXGT006243	Cellular tumor antigen p53	7157	reviewed	Transcription factor
P10415	BXGT007567	Apoptosis regulator Bcl-2	596	reviewed	Signaling
P20807	BXGT008601	Calpain-3	825	reviewed	Enzyme
P29033	BXGT009308	Gap junction beta-2 protein	2706	reviewed	Cell-cell junction
P41279	BXGT010254	Mitogen-activated protein kinase kinase kinase 8	1326	reviewed	Kinase
P46939	BXGT010555	Utrophin	7402	reviewed
P49888	BXGT010756	Estrogen sulfotransferase	6783	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}