Showing entry for Adult onset autosomal dominant leukodystrophy



                               
General Disease Information
BXGD IdBXGD018526
Disease NameAdult onset autosomal dominant leukodystrophy
Disease CUI IdC3164344
MeSH Codes   
Disease Class Name
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic 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
O00522 BXGT003935 Krev interaction trapped protein 1 889 reviewed
O15245 BXGT004141 Solute carrier family 22 member 1 6580 reviewed Transporter
P0DP23 BXGT007520 Calmodulin-1 808 reviewed
P0DP24 BXGT007521 Calmodulin-2 808 reviewed
Q7Z624 BXGT022792 Calmodulin-lysine N-methyltransferase 79823 reviewed
P0DP25 BXGT024595 Calmodulin-3 808 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