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Diseases
Genes (200)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
CFH
Membranoproliferative Glomerulonephritis
TP63
Bladder Exstrophy
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
TSLP
Membranoproliferative Glomerulonephritis
ISL1
Bladder Exstrophy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
DDX58
Singleton Merten Syndrome
SOST
Craniodiaphyseal Dysplasia
ALB
Membranoproliferative Glomerulonephritis
CFB
Membranoproliferative Glomerulonephritis
PON1
Membranoproliferative Glomerulonephritis
FH
Fumarase Deficiency
DNASE2
Membranoproliferative Glomerulonephritis