Showing entry for Contiguous ABCD1 DXS1357E deletion syndrome

General Disease Information
BXGD Id	BXGD024074
Disease Name	Contiguous ABCD1 DXS1357E deletion syndrome
Disease CUI Id	C4750847
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