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Diseases
Genes (1084)
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LMNA
Hutchinson-Gilford Progeria Syndrome
Cardiomyopathy, Dilated, 1i
Pectus Excavatum
Tauopathy
Polyhydramnios
DES
Hutchinson-Gilford Progeria Syndrome
Cardiomyopathy, Dilated, 1i
Myopathy, Myofibrillar, 1
FLNB
Pectus Excavatum
Tarsal Coalition
Polyhydramnios
Spondylocarpotarsal Synostosis Syndrome
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
Polyhydramnios
ZMPSTE24
Hutchinson-Gilford Progeria Syndrome
Polyhydramnios
MYH3
Pectus Excavatum
Tarsal Coalition
Polyhydramnios
Spondylocarpotarsal Synostosis Syndrome
TTN
Cardiomyopathy, Dilated, 1i
NDUFS2
Mitochondrial Complex I Deficiency, Nuclear Type 6
FREM1
Trigonocephaly
MAPT
Tauopathy
CFH
Membranoproliferative Glomerulonephritis
LDB3
Cardiomyopathy, Dilated, 1i
Myopathy, Myofibrillar, 1
RAF1
Cardiomyopathy, Dilated, 1i
Pectus Excavatum
Polyhydramnios
MYPN
Cardiomyopathy, Dilated, 1i
Pectus Excavatum
Polyhydramnios
TSLP
Membranoproliferative Glomerulonephritis
RBM20
Cardiomyopathy, Dilated, 1i
DMD
Cardiomyopathy, Dilated, 1i
Pectus Excavatum
TNNT2
Cardiomyopathy, Dilated, 1i
SCN5A
Cardiomyopathy, Dilated, 1i