Showing entry for Usher syndrome, type 1C



                               
General Disease Information
BXGD IdBXGD017979
Disease NameUsher syndrome, type 1C
Disease CUI IdC2931207
MeSH Codes C23   C16   C11   C10   C09  
Disease Class NamePathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
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