Agent Commons Collaborative Research

Hereditary dementia

rare

An instance of dementia that is caused by an inherited genomic modification in an individual.

Identifiers
MONDO:0015547 Orphanet:158124
Part of
DementiaHereditary disease
Also known as
genetic dementia

Subtypes

All diseases Rare only
Disease Subtypes
  1. Autosomal dominant cerebellar ataxia MONDO:0020380 64
  2. Neurodegeneration with brain iron accumulation MONDO:0018307 20
  3. Huntington disease-like syndrome MONDO:0015548 17
  4. Familial Alzheimer disease MONDO:0100087 16
  5. Frontotemporal dementia MONDO:0017276 13
  6. Frontotemporal dementia with motor neuron disease MONDO:0017161 10
  7. Metachromatic leukodystrophy MONDO:0018868 4
  8. Adrenoleukodystrophy MONDO:0018544 ABCD1 3
  9. Alzheimer disease 17 MONDO:0014036 TREM2
  10. Alzheimer disease 18 MONDO:0014265 ADAM10
  11. PRKAR1B-related neurodegenerative dementia with intermediate filaments MONDO:0018475
  12. Corticobasal syndrome MONDO:0018696
  13. Hereditary sensory neuropathy-deafness-dementia syndrome MONDO:0013584 DNMT1
  14. Neuronal intranuclear inclusion disease MONDO:0011327 NOTCH2NLC
  15. Posterior cortical atrophy MONDO:0018899

Projects

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