Showing entry for Goldenhar Syndrome



                               
General Disease Information
BXGD IdBXGD005478
Disease NameGoldenhar Syndrome
Disease CUI IdC0265240
MeSH Codes C16   C05  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:7   DOID:225  
Disease Ontology Class Namegenetic disease; disease of anatomical entity; syndrome
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
Q01538 BXGT012597 Myelin transcription factor 1 4661 reviewed Transcription factor
Q15029 BXGT013524 116 kDa U5 small nuclear ribonucleoprotein component 9343 reviewed Enzyme
Q96BZ9 BXGT019629 TBC1 domain family member 20 128637 reviewed
Q9NP72 BXGT021144 Ras-related protein Rab-18 22931 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