adisease

Showing entry for Complicated hereditary spastic paraplegia

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD008089
Disease Name	Complicated hereditary spastic paraplegia
Disease CUI Id	C0393556
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
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
P04350	BXGT006193	Tubulin beta-4A chain	10382	reviewed	Cellular structure
P54886	BXGT011092	Delta-1-pyrroline-5-carboxylate synthase	5832	reviewed	Enzyme
Q12756	BXGT013261	Kinesin-like protein KIF1A	547	reviewed	Cellular structure
Q16595	BXGT013643	Frataxin, mitochondrial	2395	reviewed	Enzyme
Q8TD30	BXGT018805	Alanine aminotransferase 2	84706	reviewed	Enzyme

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}