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 71 - 80 of 108 in total
HPO ID HPO Term
HP:0008046 Abnormal retinal vascular morphology
HP:0008516 Abnormality of the vertebral spinous processes
HP:0009811 Abnormality of the elbow
HP:0009830 Peripheral neuropathy
HP:0010530 Palatal tremor
HP:0010874 Tendon xanthomatosis
HP:0011931 Abnormal cerebellar peduncle morphology
HP:0011994 Abnormal atrial septum morphology
HP:0012075 Personality disorder
HP:0012379 Abnormal circulating enzyme concentration or activity
Displaying 1 entry
Gene ID Gene Symbol Description
1593 CYP27A1 cytochrome P450 family 27 subfamily A member 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024