adisease

Showing entry for MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD022108
Disease Name	MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL
Disease CUI Id	C4084823
MeSH Codes
Disease Class Name
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
P02708	BXGT005927	Acetylcholine receptor subunit alpha	1134	reviewed	Ion channel
P11230	BXGT007677	Acetylcholine receptor subunit beta	1140	reviewed	Ion channel
Q04844	BXGT012789	Acetylcholine receptor subunit epsilon	1145	reviewed	Ion channel
Q07001	BXGT012907	Acetylcholine receptor subunit delta	1144	reviewed	Ion channel

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}