Showing entry for Retinitis Pigmentosa

General Disease Information
BXGD Id	BXGD002539
Disease Name	Retinitis Pigmentosa
Disease CUI Id	C0035334
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	HP:0000478
Human Phenotype Ontology Term	Abnormality of the eye
Disease Ontology Id	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations