-
APP
- Cerebral Amyloid Angiopathy, App-Related
- Inclusion Body Myositis
- Alzheimer Disease
- Alzheimer's Disease
- Fraxe Intellectual Disability
- Fragile X Syndrome
- Cerebral Amyloid Angiopathy
- Amyloidosis
- Leukoencephalopathy
- Endogenous Depression
- Pick Disease Of Brain
- Hereditary Cystatin C Amyloid Angiopathy
- Neurodegeneration
- Supranuclear Palsy, Progressive, 1
- Mild Cognitive Impairment
- MAPT
- PSEN1
-
APOE
- Cerebral Amyloid Angiopathy, App-Related
- Inclusion Body Myositis
- Alzheimer Disease
- Alzheimer's Disease
- Cerebral Amyloid Angiopathy
- Amyloidosis
- Chmp2b Frontotemporal Dementia
- Leukoencephalopathy
- Pick Disease Of Brain
- Primary Cutaneous Amyloidosis
- Hearing Loss
- Neurodegeneration
- Supranuclear Palsy, Progressive, 1
- Apathy
- Retinal Diseases
- Mild Cognitive Impairment
-
CST3
- Cerebral Amyloid Angiopathy, App-Related
- Inclusion Body Myositis
- Alzheimer Disease
- Alzheimer's Disease
- Cerebral Amyloid Angiopathy
- Amyloidosis
- Heredofamilial Amyloidosis
- Leukoencephalopathy
- Hereditary Cystatin C Amyloid Angiopathy
- Neurodegeneration
- Supranuclear Palsy, Progressive, 1
- Retinal Diseases
- Mild Cognitive Impairment
- ADAM10
- TREM2
- BDNF
- HMOX1
- ACE
- GSK3B
- FMR1
- MTHFR
- TTR
- CASP3
- CHMP2B
- NPY
- ACHE
- TOMM40
- IL1B