Showing entry for CONE DYSTROPHY, X-LINKED, 1

General Disease Information
BXGD Id	BXGD014675
Disease Name	CONE DYSTROPHY, X-LINKED, 1
Disease CUI Id	C1844777
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