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Diseases
Genes (464)
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SCN5A
Cardiac Conduction Defect
SH2D1A
X-Linked Lymphoproliferative Disease
LRP5
Osteoporosis-Pseudoglioma Syndrome
L2HGDH
L-2-Hydroxyglutaric Aciduria
NOS2
Silicosis
Asbestosis
ARG1
Silicosis
Asbestosis
MECP2
Lubs X-Linked Mental Retardation Syndrome
PEX1
Peroxisome Biogenesis Disorder 10a (Zellweger)
TNF
Silicosis
Asbestosis
Q Fever
IL1B
Silicosis
Asbestosis
Bursitis
X-Linked Lymphoproliferative Disease
Membranoproliferative Glomerulonephritis
Cystinosis
EXOSC2
Short Stature, Hearing Loss, Retinitis Pigmentosa, And Distinctive Facies
CFH
Membranoproliferative Glomerulonephritis
ATPAF2
Mitochondrial Complex V (Atp Synthase) Deficiency, Nuclear Type 1
CCL2
Silicosis
Membranoproliferative Glomerulonephritis
Cystinosis
Q Fever
PEX3
Peroxisome Biogenesis Disorder 10a (Zellweger)
PEX6
Peroxisome Biogenesis Disorder 10a (Zellweger)
IL17A
Silicosis
X-Linked Lymphoproliferative Disease
PEX16
Peroxisome Biogenesis Disorder 10a (Zellweger)
PEX2
Peroxisome Biogenesis Disorder 10a (Zellweger)
PEX12
Peroxisome Biogenesis Disorder 10a (Zellweger)