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Diseases
Genes (263)
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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
CFH
Membranoproliferative Glomerulonephritis
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
TSLP
Membranoproliferative Glomerulonephritis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
ALB
Membranoproliferative Glomerulonephritis
Protein Losing Enteropathy
DDX58
Singleton Merten Syndrome
CFB
Membranoproliferative Glomerulonephritis
PON1
Membranoproliferative Glomerulonephritis
AKR1C3
True Hermaphroditism
AKR1C1
True Hermaphroditism
AKR1C2
True Hermaphroditism
HSD17B3
True Hermaphroditism
LHCGR
True Hermaphroditism
DNASE2
Membranoproliferative Glomerulonephritis