Showing entry for Retinitis Pigmentosa 4



                               
General Disease Information
BXGD IdBXGD018373
Disease NameRetinitis Pigmentosa 4
Disease CUI IdC3151001
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