Showing entry for Congenital Hydrocephalus



                               
General Disease Information
BXGD IdBXGD001370
Disease NameCongenital Hydrocephalus
Disease CUI IdC0020256
MeSH Codes C10  
Disease Class NameNervous System Diseases
Semantic TypeCongenital Abnormality
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease 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
A4D126 BXGT001208 D-ribitol-5-phosphate cytidylyltransferase 729920 reviewed
A6NCL1 BXGT001462 Geminin coiled-coil domain-containing protein 1 647309 reviewed
O15550 BXGT004179 Lysine-specific demethylase 6A 7403 reviewed Epigenetic regulator
P13497 BXGT007915 Bone morphogenetic protein 1 649 reviewed
P15328 BXGT008108 Folate receptor alpha 2348 reviewed
P30279 BXGT009415 G1/S-specific cyclin-D2 894 reviewed Enzyme modulator
P32004 BXGT009594 Neural cell adhesion molecule L1 3897 reviewed
P39748 BXGT010134 Flap endonuclease 1 2237 reviewed Enzyme
P42785 BXGT010338 Lysosomal Pro-X carboxypeptidase 5547 reviewed Enzyme
P42858 BXGT010341 Huntingtin 3064 reviewed
Q96L92 BXGT019690 Sorting nexin-27 81609 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