ITM2B-related cerebral amyloid angiopathy 2

Summary
Synonym
  • Cerebellar Ataxia, Cataract, Deafness, and Dementia Or Psychosis
  • FDD
  • Familial Danish Dementia
  • HOOE
  • Heredopathia Ophthalmootoencephalica
Definition
A cerebral amyloid angiopathy characterized by ataxia, intention tremor, psychosis and dementia that has_material_basis_in an autosomal dominant mutation of the ITM2B gene on chromosome 13q14.2.
Super Class
autosomal dominant disease cerebral amyloid angiopathy
Disease Ontology
DOID:0070030
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9445 ITM2B integral membrane protein 2B
Displaying 1 entry
Gene ID Gene Symbol Description Source
16432 Itm2b integral membrane protein 2B
Displaying 1 entry
Gene ID Gene Symbol Description Source
290364 Itm2b integral membrane protein 2B
Displaying 1 entry
Gene ID Gene Symbol Description Source
180816 itm-2 Integral membrane protein 2

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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: December 9, 2024