adisease

Showing entry for CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD016411
Disease Name	CHARCOT-MARIE-TOOTH DISEASE, TYPE 4C
Disease CUI Id	C1866636
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
O95235	BXGT005360	Kinesin-like protein KIF20A	10112	reviewed	Cellular structure
P62491	BXGT011430	Ras-related protein Rab-11A	8766	reviewed
Q01453	BXGT012588	Peripheral myelin protein 22	5376	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}