Showing entry for PEROXISOME BIOGENESIS DISORDER 2B

General Disease Information
BXGD Id	BXGD019133
Disease Name	PEROXISOME BIOGENESIS DISORDER 2B
Disease CUI Id	C3550234
MeSH Codes	C16   C18
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations