Showing entry for RETINITIS PIGMENTOSA 1

General Disease Information
BXGD Id	BXGD004325
Disease Name	RETINITIS PIGMENTOSA 1
Disease CUI Id	C0220701
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:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations