ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL
General Information (adopted from Orphanet):
Synonyms, Signs: |
|
Number of Symptoms | 7 |
OrphanetNr: | |
OMIM Id: |
502500
|
ICD-10: |
|
UMLs: |
|
MeSH: |
|
MedDRA: |
|
Snomed: |
|
Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
|
Age of onset: |
|
Disease classification (adopted from Orphanet):
Parent Diseases: | No data available. |
Symptom Information:
|
(HPO:0001300) | Parkinsonism | 75 / 7739 | ||||
|
(HPO:0002511) | Alzheimer disease | 10 / 7739 | ||||
|
(HPO:0000726) | Dementia | 131 / 7739 | ||||
|
(HPO:0003584) | Late onset | 10 / 7739 | ||||
|
(HPO:0002423) | Long-tract signs | 7 / 7739 | ||||
|
(HPO:0002185) | Neurofibrillary tangles | 14 / 7739 | ||||
|
(OMIM) | Presenile and senile dementia. Parkinsonism. Long tract signs. | 1 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
---|