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DO Term : cerebrotendinous xanthomatosis [DOID:4810] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A xanthomatosis that is characterized by a deficiency in the production of the bile acid, chenodeoxycholic acid that has_material_basis_in homozygous or compound heterozygous mutation in the CYP27A1 gene, which encodes sterol 27-hydroxylase, on chromosome 2q35.
  • synonyms:
  • SNOMEDCT_US_2023_03_01:63246000,
  • UMLS_CUI:C0238052,
  • GARD:5622,
  • 213700,
  • NCI:C84628,
  • Cholestanol storage disease,
  • MESH:D019294,
  • OMIM:213700,
  • ORDO:909
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Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents