Alzheimer disease 3
- Synonyms
- ALZHEIMER DISEASE, FAMILIAL, 3; Alzheimer disease early onset type 3
Summary
Available tests
Check Related conditions for additional relevant tests.
Clinical features
Help- Abnormality of the digestive system
- Dysphagia
Dysphagia
- MedGen UID: 41440
- Concept ID: C0011168
- Finding: Disease or Syndrome
Abnormality of the digestive system
- Dysphagia
- Abnormality of the nervous system
- Abnormality of extrapyramidal motor function
Abnormality of extrapyramidal motor function
- MedGen UID: 115941
- Concept ID: C0234133
- Finding: Sign or Symptom
Abnormality of the nervous system
- Agnosia
Agnosia
- MedGen UID: 174
- Concept ID: C0001816
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Alzheimer disease
Alzheimer disease
- MedGen UID: 1853
- Concept ID: C0002395
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Apraxia
Apraxia
- MedGen UID: 8166
- Concept ID: C0003635
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Babinski sign
Babinski sign
- MedGen UID: 19708
- Concept ID: C0034935
- Finding: Finding
Abnormality of the nervous system
- Cerebral cortical atrophy
Cerebral cortical atrophy
- MedGen UID: 1646740
- Concept ID: C4551583
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Dementia
Dementia
- MedGen UID: 99229
- Concept ID: C0497327
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Dysarthria
Dysarthria
- MedGen UID: 8510
- Concept ID: C0013362
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Dystonic disorder
Dystonic disorder
- MedGen UID: 3940
- Concept ID: C0013421
- Finding: Sign or Symptom
Abnormality of the nervous system
- Gait disturbance
Gait disturbance
- MedGen UID: 107895
- Concept ID: C0575081
- Finding: Finding
Abnormality of the nervous system
- Lower limb hyperreflexia
Lower limb hyperreflexia
- MedGen UID: 322973
- Concept ID: C1836696
- Finding: Finding
Abnormality of the nervous system
- Memory impairment
Memory impairment
- MedGen UID: 68579
- Concept ID: C0233794
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Myoclonus
Myoclonus
- MedGen UID: 10234
- Concept ID: C0027066
- Finding: Finding
Abnormality of the nervous system
- Neurofibrillary tangles
Neurofibrillary tangles
- MedGen UID: 39273
- Concept ID: C0085400
- Finding: Finding
Abnormality of the nervous system
- Optic ataxia
Optic ataxia
- MedGen UID: 1635801
- Concept ID: C4703584
- Finding: Finding
Abnormality of the nervous system
- Personality changes
Personality changes
- MedGen UID: 66817
- Concept ID: C0240735
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Seizure
Seizure
- MedGen UID: 20693
- Concept ID: C0036572
- Finding: Sign or Symptom
Abnormality of the nervous system
- Spastic tetraparesis
Spastic tetraparesis
- MedGen UID: 658719
- Concept ID: C0575059
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Abnormality of extrapyramidal motor function
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.