cerebrotendinous xanthomatosis

Summary
Synonym
  • Cholestanol storage disease
Definition
A xanthomatosis that is characterized by a deficiency in the production of the bile acid, chenodeoxycholic acid that has_material_basis_in autosomal recessive inheritance and results in cholestanol deposition in the brain and other tissues and with elevated levels of cholesterol in plasma.
Super Class
xanthomatosis
External Links
Disease Ontology
DOID:4810
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
WikiPathways (from TogoID)
Related Genes
Displaying all 8 entries
Gene ID Gene Symbol Description Source
1555 CYP2B6 cytochrome P450 family 2 subfamily B member 6
1576 CYP3A4 cytochrome P450 family 3 subfamily A member 4
1593 CYP27A1 cytochrome P450 family 27 subfamily A member 1
1594 CYP27B1 cytochrome P450 family 27 subfamily B member 1
3290 HSD11B1 hydroxysteroid 11-beta dehydrogenase 1
3291 HSD11B2 hydroxysteroid 11-beta dehydrogenase 2
5730 PTGDS prostaglandin D2 synthase
124872 B4GALNT2 beta-1,4-N-acetyl-galactosaminyltransferase 2 (SID blood group)
The Human Phenotype Ontology
Displaying entries 51 - 60 of 108 in total
HPO ID HPO Term
HP:0002659 Increased susceptibility to fractures
HP:0002823 Abnormal femur morphology
HP:0002942 Thoracic kyphosis
HP:0002992 Abnormal tibia morphology
HP:0003474 Somatic sensory dysfunction
HP:0003487 Babinski sign
HP:0003693 Distal amyotrophy
HP:0004416 Precocious atherosclerosis
HP:0005109 Abnormality of the Achilles tendon
HP:0005181 Premature coronary artery atherosclerosis
Displaying 1 entry
Gene ID Gene Symbol Description
1593 CYP27A1 cytochrome P450 family 27 subfamily A member 1

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Last updated: August 19, 2024