Showing entry for Achromatopsia 2



                               
General Disease Information
BXGD IdBXGD015721
Disease NameAchromatopsia 2
Disease CUI IdC1857618
MeSH Codes C23   C11   C10  
Disease Class NamePathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0000478  
Human Phenotype Ontology TermAbnormality of the eye
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease of anatomical entity
Disorder Network disorder-protein-compound-food associations