Showing entry for Retinitis Pigmentosa 46

General Disease Information
BXGD Id	BXGD017293
Disease Name	Retinitis Pigmentosa 46
Disease CUI Id	C2675496
MeSH Codes	C16   C11
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations