adisease

Showing entry for CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder)

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD013902
Disease Name	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder)
Disease CUI Id	C1833219
MeSH Codes	C16 C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
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
O15269	BXGT004145	Serine palmitoyltransferase 1	10558	reviewed	Enzyme
P01138	BXGT005738	Beta-nerve growth factor	4803	reviewed	Signaling
P51149	BXGT010835	Ras-related protein Rab-7a	7879	reviewed
Q9NP72	BXGT021144	Ras-related protein Rab-18	22931	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}