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Diseases
Genes (196)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
CFH
Membranoproliferative Glomerulonephritis
TP63
Bladder Exstrophy
ASS1
Citrullinemia Type I
TSLP
Membranoproliferative Glomerulonephritis
ISL1
Bladder Exstrophy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
SOST
Klippel-Trenaunay-Weber Syndrome
Craniodiaphyseal Dysplasia
DDX58
Singleton Merten Syndrome
ALB
Membranoproliferative Glomerulonephritis
CFB
Membranoproliferative Glomerulonephritis
PON1
Membranoproliferative Glomerulonephritis
DNASE2
Membranoproliferative Glomerulonephritis
C1QA
Membranoproliferative Glomerulonephritis
FH
Fumarase Deficiency