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Diseases
Genes (212)
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SLC6A19
Hartnup Disease
PMM2
Pmm2 Deficiency
ASL
Argininosuccinic Aciduria
SLC12A6
Andermann Syndrome
TTPA
Familial Isolated Vitamin E 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
ALB
Membranoproliferative Glomerulonephritis
CFB
Membranoproliferative Glomerulonephritis
PON1
Membranoproliferative Glomerulonephritis
SOST
Craniodiaphyseal Dysplasia
DNASE2
Membranoproliferative Glomerulonephritis