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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:hereditary dementia
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Accession:EFO:MONDO:0015547 term browser browse the term
Definition:An instance of dementia that is caused by an inherited genomic modification in an individual.
Synonyms:exact_synonym: Orphanet:158124;   genetic dementia;   http://identifiers.org/medgen/1842422;   http://linkedlifedata.com/resource/umls/id/C5680680
 alt_id: MONDO:0015547
 xref: GARD:20028;   MEDGEN:1842422;   ORDO:158124;   UMLS:C5680680


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Term paths to the root
Path 1
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          genetic disorder 0
            hereditary dementia 0
              Alzheimer disease 18 0
              Huntington disease-like syndrome + 0
              Lewy body dementia 0
              adrenoleukodystrophy + 0
              autosomal dominant cerebellar ataxia + 0
              bilateral striopallidodentate calcinosis + 0
              cerebral lipidosis with dementia + 0
              corticobasal syndrome 0
              familial Alzheimer disease + 0
              frontotemporal dementia + 0
              frontotemporal dementia with motor neuron disease + 0
              hereditary sensory neuropathy-deafness-dementia syndrome 0
              metachromatic leukodystrophy + 0
              neurodegeneration with brain iron accumulation + 0
              neuronal intranuclear inclusion disease 0
              posterior cortical atrophy 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          nervous system disease 0
            central nervous system disease 0
              brain disease 0
                mental or behavioural disorder 0
                  cognitive disorder 0
                    dementia 0
                      hereditary dementia 0
                        Alzheimer disease 18 0
                        Huntington disease-like syndrome + 0
                        Lewy body dementia 0
                        adrenoleukodystrophy + 0
                        autosomal dominant cerebellar ataxia + 0
                        bilateral striopallidodentate calcinosis + 0
                        cerebral lipidosis with dementia + 0
                        corticobasal syndrome 0
                        familial Alzheimer disease + 0
                        frontotemporal dementia + 0
                        frontotemporal dementia with motor neuron disease + 0
                        hereditary sensory neuropathy-deafness-dementia syndrome 0
                        metachromatic leukodystrophy + 0
                        neurodegeneration with brain iron accumulation + 0
                        neuronal intranuclear inclusion disease 0
                        posterior cortical atrophy 0
paths to the root