Showing entry for Retinal Dystrophy, Early-Onset Severe, Lrat-Related



                               
General Disease Information
BXGD IdBXGD017644
Disease NameRetinal Dystrophy, Early-Onset Severe, Lrat-Related
Disease CUI IdC2750064
MeSH Codes C16   C11  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease of anatomical entity
Disorder Network disorder-protein-compound-food associations