Showing entry for Neurodevelopmental abnormality



                               
General Disease Information
BXGD IdBXGD020973
Disease NameNeurodevelopmental abnormality
Disease CUI IdC4022737
MeSH Codes   
Disease Class Name
Semantic TypePathologic Function
Human Phenotype Ontology Id HP:0000707  
Human Phenotype Ontology TermAbnormality of the nervous system
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
O43497 BXGT004596 Voltage-dependent T-type calcium channel subunit alpha-1G 8913 reviewed Ion channel
P19367 BXGT008476 Hexokinase-1 3098 reviewed Kinase
P41229 BXGT010239 Lysine-specific demethylase 5C 8242 reviewed
P55263 BXGT011115 Adenosine kinase 132 reviewed Kinase
Q14204 BXGT013456 Cytoplasmic dynein 1 heavy chain 1 1778 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