-
APP
- Early-Onset Autosomal Dominant Alzheimer Disease
- Alzheimer's Disease
- Cerebral Amyloid Angiopathy, App-Related
- Inclusion Body Myositis
- Fragile X Syndrome
- Fraxe Intellectual Disability
- Hereditary Cerebral Hemorrhage With Amyloidosis
- Amyloidosis
- Leukoencephalopathy
- Supranuclear Palsy, Progressive, 1
- Pick Disease Of Brain
- Hereditary Cystatin C Amyloid Angiopathy
- Familial Amyloid Polyneuropathy
- Neurodegeneration
- Stroke, Ischemic
- Gerstmann-Straussler Disease
- Splenomegaly
- MAPT
- PSEN1
-
APOE
- Early-Onset Autosomal Dominant Alzheimer Disease
- Alzheimer's Disease
- Cerebral Amyloid Angiopathy, App-Related
- Inclusion Body Myositis
- Hereditary Cerebral Hemorrhage With Amyloidosis
- Amyloidosis
- Leukoencephalopathy
- Supranuclear Palsy, Progressive, 1
- Pick Disease Of Brain
- Primary Cutaneous Amyloidosis
- Hearing Loss
- Neurodegeneration
- Stroke, Ischemic
- Gerstmann-Straussler Disease
- Splenomegaly
- ADAM10
- TREM2
-
CST3
- Early-Onset Autosomal Dominant Alzheimer Disease
- Alzheimer's Disease
- Cerebral Amyloid Angiopathy, App-Related
- Inclusion Body Myositis
- Hereditary Cerebral Hemorrhage With Amyloidosis
- Amyloidosis
- Heredofamilial Amyloidosis
- Leukoencephalopathy
- Supranuclear Palsy, Progressive, 1
- Hereditary Cystatin C Amyloid Angiopathy
- Neurodegeneration
- Stroke, Ischemic
- TTR
- PRNP
- BDNF
- ACE
- IL1B
- HMOX1
- FMR1
- HFE
- GSK3B
- ABCA7
- CASP3
- TOMM40
- BACE1