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Diseases
Genes (311)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
Renpenning's Syndrome
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
TP63
Bladder Exstrophy
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
TSLP
Membranoproliferative Glomerulonephritis
ISL1
Bladder Exstrophy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
DDX58
Singleton Merten Syndrome
ALB
Membranoproliferative Glomerulonephritis
Protein Losing Enteropathy
SOST
Craniodiaphyseal Dysplasia
CFB
Membranoproliferative Glomerulonephritis
PON1
Membranoproliferative Glomerulonephritis
DNASE2
Membranoproliferative Glomerulonephritis
C1QA
Membranoproliferative Glomerulonephritis