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Accession:DOID:0111036 term browser browse the term
Definition:A CADASIL characterized by stroke, transient ischemic attacks, cognitive impairment, dementia, balance impairment, gait disturbance, headaches, and/or seizures associated with early confluent or confluent diffuse white matter hyperintensities that has_material_basis_in heterozygous mutation in the HTRA1 gene on chromosome 10q26. (DO)
Synonyms:exact_synonym: CADASIL2;   autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2
 primary_id: OMIM:616779
 xref: ICD10CM:F01.1
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CADASIL 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Htra1 HtrA serine peptidase 1 JBrowse link 1 201,499,067 201,548,508 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 0
    Diseases of the Aged 1210
      dementia 652
        vascular dementia 40
          CADASIL 2
            CADASIL 2 1
Path 2
Term Annotations click to browse term
  disease 15851
    disease of anatomical entity 15243
      nervous system disease 10713
        central nervous system disease 8827
          brain disease 8119
            disease of mental health 5752
              cognitive disorder 1881
                dementia 652
                  vascular dementia 40
                    CADASIL 2
                      CADASIL 2 1
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