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Diseases
Genes (2496)
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APP
Cerebral Amyloid Angiopathy, App-Related
Inclusion Body Myositis
Neurodegeneration
Pick Disease Of Brain
Hereditary Cerebral Amyloid Angiopathy
Abetal34v Amyloidosis
LRRK2
Neurodegeneration
Parkinson Disease 8, Autosomal Dominant
HMOX1
Neurodegeneration
Focal Segmental Glomerulosclerosis
Primary Ovarian Insufficiency
Spinocerebellar Ataxia Type 17
Hemolytic Anemia
PSEN1
Cerebral Amyloid Angiopathy, App-Related
Neurodegeneration
Pick Disease Of Brain
Hemolytic Anemia
MAPT
Inclusion Body Myositis
Neurodegeneration
Pick Disease Of Brain
TRPC6
Focal Segmental Glomerulosclerosis
ZFPM2
Tetralogy Of Fallot
TBP
Neurodegeneration
Spinocerebellar Ataxia Type 17
NKX2-5
Tetralogy Of Fallot
COL4A1
Focal Segmental Glomerulosclerosis
Amblyopia
Hemolytic Anemia
TBX1
Amblyopia
Tetralogy Of Fallot
EPO
Neurodegeneration
Hemolytic Anemia
Thalassemia
INF2
Neurodegeneration
Focal Segmental Glomerulosclerosis
JAG1
Tetralogy Of Fallot
GATA4
Tetralogy Of Fallot
G6PD
Neurodegeneration
Hemolytic Anemia
Color Blindness
Thalassemia
SUFU
Joubert Syndrome 32
Tetralogy Of Fallot
GATA6
Tetralogy Of Fallot
GRN
Neurodegeneration
Pick Disease Of Brain
ADAM10
Neurodegeneration
Alzheimer Disease 18