Showing entry for Joubert syndrome 1

General Disease Information
BXGD Id	BXGD023356
Disease Name	Joubert syndrome 1
Disease CUI Id	C4551568
MeSH Codes	C16   C13   C11   C12
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Male Urogenital Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7   DOID:225
Disease Ontology Class Name	genetic disease; disease of anatomical entity; syndrome
Disorder Network	disorder-protein-compound-food associations