adisease

Showing entry for Peroneal muscular atrophy (axonal type) (hypertrophic type)

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD017836
Disease Name	Peroneal muscular atrophy (axonal type) (hypertrophic type)
Disease CUI Id	C2875300
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
P02545	BXGT005889	Prelamin-A/C	4000	reviewed
P08034	BXGT006716	Gap junction beta-1 protein	2705	reviewed	Cell-cell junction
P41250	BXGT010244	Glycine--tRNA ligase	2617	reviewed	Enzyme
Q01453	BXGT012588	Peripheral myelin protein 22	5376	reviewed	Cellular structure
Q14204	BXGT013456	Cytoplasmic dynein 1 heavy chain 1	1778	reviewed	Enzyme
O95140	BXGT024482	Mitofusin-2	9927	reviewed	Enzyme
Q96HY7	BXGT025609	Probable 2-oxoglutarate dehydrogenase E1 component DHKTD1, mitochondrial	55526	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}