Showing entry for Usher Syndrome, Type IF



                               
General Disease Information
BXGD IdBXGD016352
Disease NameUsher Syndrome, Type IF
Disease CUI IdC1865885
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 DOID:630   DOID:225  
Disease Ontology Class Namegenetic disease; syndrome
Disorder Network disorder-protein-compound-food associations