Showing entry for Lissencephaly with cerebellar hypoplasia



                               
General Disease Information
BXGD IdBXGD022358
Disease NameLissencephaly with cerebellar hypoplasia
Disease CUI IdC4274995
MeSH Codes C16   C10   F03  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
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
Q00535 BXGT012534 Cyclin-dependent-like kinase 5 1020 reviewed Kinase
Q71U36 BXGT016705 Tubulin alpha-1A chain 7846 reviewed Cellular structure
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