-
APP
- Cerebral Amyloid Angiopathy, App-Related
- Inclusion Body Myositis
- Alzheimer Disease
- Alzheimer's Disease
- Fraxe Intellectual Disability
- Cerebral Amyloid Angiopathy
- Fragile X Syndrome
- Amyloidosis
- Leukoencephalopathy
- Cognitive Deficit
- Myelopathy
- Pick Disease Of Brain
- Hereditary Cystatin C Amyloid Angiopathy
- Neurogenic Inflammation
- Endogenous Depression
- Neurodegeneration
- Familial Amyloid Polyneuropathy
- Paralysis
- Supranuclear Palsy, Progressive, 1
- Splenomegaly
- MAPT
- PSEN1
-
APOE
- Cerebral Amyloid Angiopathy, App-Related
- Inclusion Body Myositis
- Alzheimer Disease
- Alzheimer's Disease
- Cerebral Amyloid Angiopathy
- Amyloidosis
- Leukoencephalopathy
- Cognitive Deficit
- Myelopathy
- Pick Disease Of Brain
- Primary Cutaneous Amyloidosis
- Hearing Loss
- Neurodegeneration
- Apathy
- Supranuclear Palsy, Progressive, 1
- Splenomegaly
- TREM2
-
CST3
- Cerebral Amyloid Angiopathy, App-Related
- Inclusion Body Myositis
- Alzheimer Disease
- Alzheimer's Disease
- Cerebral Amyloid Angiopathy
- Amyloidosis
- Heredofamilial Amyloidosis
- Leukoencephalopathy
- Cognitive Deficit
- Hereditary Cystatin C Amyloid Angiopathy
- Neurodegeneration
- Supranuclear Palsy, Progressive, 1
- ADAM10
- TTR
- BDNF
- FMR1
- GSK3B
- MTHFR
- BCHE
- TNF
- ACE
- HMOX1
- IL1B
- HFE
- ACHE
- CRH