Showing entry for Pontocerebellar Hypoplasia Type 1

General Disease Information
BXGD Id	BXGD014589
Disease Name	Pontocerebellar Hypoplasia Type 1
Disease CUI Id	C1843504
MeSH Codes	C16   C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic Type	Disease or Syndrome; Congenital Abnormality
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