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: Sort by abundance 

1
(HPO:0001300) Parkinsonism 75 / 7739
2
(HPO:0002511) Alzheimer disease 10 / 7739
3
(HPO:0000726) Dementia 131 / 7739
4
(HPO:0003584) Late onset 10 / 7739
5
(HPO:0002423) Long-tract signs 7 / 7739
6
(HPO:0002185) Neurofibrillary tangles 14 / 7739
7
(OMIM) Presenile and senile dementia. Parkinsonism. Long tract signs. 1 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: