Showing entry for Contiguous Abcd1-Dxs1375e Deletion Syndrome

General Disease Information
BXGD Id	BXGD014746
Disease Name	Contiguous Abcd1-Dxs1375e Deletion Syndrome
Disease CUI Id	C1845408
MeSH Codes	C16
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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