adisease

Showing entry for Neuromuscular dysphagia

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD021761
Disease Name	Neuromuscular dysphagia
Disease CUI Id	C4025729
MeSH Codes	C06 C09
Disease Class Name	Digestive System Diseases; Otorhinolaryngologic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id	HP:0025031 HP:0000707
Human Phenotype Ontology Term	Abnormality of the digestive system; Abnormality of the nervous system
Disease Ontology Id
Disease Ontology Class Name
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
O95363	BXGT005375	Phenylalanine--tRNA ligase, mitochondrial	10667	reviewed	Enzyme
P06753	BXGT006498	Tropomyosin alpha-3 chain	7170	reviewed	Cellular structure
P10636	BXGT007596	Microtubule-associated protein tau	4137	reviewed
P68133	BXGT011578	Actin, alpha skeletal muscle	58	reviewed	Cellular structure

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}