ORPHA:98534
Neurodegenerative disease with dementia
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Neurodegenerative disease with dementia | |
| fr | Maladie neurodégénérative avec démence | |
| de | Neurodegenerative Krankheit mit Demenz | |
| es | Enfermedad neurodegenerativa con demencia | |
| it | Malattia neurodegenerativa con demenza | |
| nl | Neurodegeneratieve ziekte met dementie | |
| pt | Demência associada com doença neurodegenerativa | |
| pl | Choroba neurodegeneracyjna z otępieniem | |
| cs | Neurodegenerativní choroby s demencí | |
| uk | Нейродегенеративне захворювання з деменцією | |
| zh | 神经退行性疾病伴痴呆 | |
| tr | Demans ile seyreden nörodejeneratif hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681723 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:89043Rare dementia
rare neurological diseases - ORPHA:182070Rare neurodegenerative disease
rare neurological diseases
Children (19):
- ORPHA:313808Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
- ORPHA:98538Ataxia with dementia
- ORPHA:1020Early-onset autosomal dominant Alzheimer disease
- ORPHA:98535Frontotemporal degeneration with dementia
- ORPHA:411602Hereditary late-onset Parkinson disease
- ORPHA:456318Hereditary sensory neuropathy-deafness-dementia syndrome
- ORPHA:56970Human prion disease
- ORPHA:399Huntington disease
- ORPHA:401901Huntington disease-like syndrome due to C9ORF72 expansions
- ORPHA:439254ITM2B amyloidosis
- ORPHA:248111Juvenile Huntington disease
- ORPHA:2770Nasu-Hakola disease
- ORPHA:263440Neuroacanthocytosis
- ORPHA:385Neurodegeneration with brain iron accumulation
- ORPHA:2289Neuronal intranuclear inclusion disease
- ORPHA:412066PRKAR1B-related neurodegenerative dementia with intermediate filaments
- ORPHA:90020Parkinson-dementia complex of Guam
- ORPHA:54247Posterior cortical atrophy
- ORPHA:95432Primary progressive aphasia
Codes that Orphanet moved or referred to this one:
- ORPHA:97342OBSOLETE: Argyrophilic grain disease referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/98534
- This record as JSON: /data/d/98534.json