Alzheimer disease
Symptom Information:
Symptom ID: | HPO:0002511 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) Alzheimer disease(HPO:0002511) MedDRA: Nervous system disorders(MedDRA:10029205) Mental impairment disorders(MedDRA:10057167) Alzheimer disease(HPO:0002511) |
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Database Frequency: | 10 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
ALZHEIMER DISEASE 10 | (OMIM:609636) |
ALZHEIMER DISEASE 2 | (OMIM:104310) |
ALZHEIMER DISEASE 3 | (OMIM:607822) |
ALZHEIMER DISEASE 4 | (OMIM:606889) |
ALZHEIMER DISEASE 5 | (OMIM:602096) |
ALZHEIMER DISEASE, FAMILIAL EARLY-ONSET, WITH COEXISTING AMYLOID ANDPRION PATHOLOGY | (OMIM:605055) |
ALZHEIMER DISEASE, SUSCEPTIBILITY TO, MITOCHONDRIAL | (OMIM:502500) |
APOLIPOPROTEIN E | (OMIM:107741) |
Down syndrome | (Orphanet:870) |
Early-onset autosomal dominant Alzheimer disease | (Orphanet:1020) |