Showing entry for Heredodegenerative Disorders, Nervous System



                               
General Disease Information
BXGD IdBXGD010622
Disease NameHeredodegenerative Disorders, Nervous System
Disease CUI IdC0751870
MeSH Codes C16   C10  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic TypeDisease 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
O15118 BXGT004127 NPC intracellular cholesterol transporter 1 4864 reviewed Transporter
P02766 BXGT005953 Transthyretin 7276 reviewed Transporter
P02792 BXGT005966 Ferritin light chain 2512 reviewed Storage
P09874 BXGT006934 Poly [ADP-ribose] polymerase 1 142 reviewed
P15289 BXGT008102 Arylsulfatase A 410 reviewed Enzyme
P18887 BXGT008437 DNA repair protein XRCC1 7515 reviewed
P42858 BXGT010341 Huntingtin 3064 reviewed
Q16595 BXGT013643 Frataxin, mitochondrial 2395 reviewed Enzyme
Q16637 BXGT013646 Survival motor neuron protein 6607 reviewed Epigenetic regulator
Q8WWM9 BXGT019001 Cytoglobin 114757 reviewed
Q9NPG2 BXGT021155 Neuroglobin 58157 reviewed Transporter
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