An instance of dementia that is caused by an inherited genomic modification in an individual.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Autosomal dominant cerebellar ataxia | MONDO:0020380 | 64 | |
| Neurodegeneration with brain iron accumulation | MONDO:0018307 | 20 | |
| Huntington disease-like syndrome | MONDO:0015548 | 17 | |
| Familial Alzheimer disease | MONDO:0100087 | 16 | |
| Frontotemporal dementia | MONDO:0017276 | 13 | |
| Frontotemporal dementia with motor neuron disease | MONDO:0017161 | 10 | |
| Metachromatic leukodystrophy | MONDO:0018868 | 4 | |
| Adrenoleukodystrophy | MONDO:0018544 | 3 | ABCD1 |
| Alzheimer disease 17 | MONDO:0014036 | TREM2 | |
| Alzheimer disease 18 | MONDO:0014265 | ADAM10 | |
| PRKAR1B-related neurodegenerative dementia with intermediate filaments | MONDO:0018475 | ||
| Corticobasal syndrome | MONDO:0018696 | ||
| Hereditary sensory neuropathy-deafness-dementia syndrome | MONDO:0013584 | DNMT1 | |
| Neuronal intranuclear inclusion disease | MONDO:0011327 | NOTCH2NLC | |
| Posterior cortical atrophy | MONDO:0018899 |
Rare disease
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