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Diseases
Genes (230)
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GH1
Kowarski Syndrome
Fibrous Dysplasia Of Bone
SLC12A6
Andermann Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
C3
Complement Component 3 Deficiency, Autosomal Recessive
Membranoproliferative Glomerulonephritis
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
DNASE2
Membranoproliferative Glomerulonephritis
C1QA
Membranoproliferative Glomerulonephritis
TGFBR2
Membranoproliferative Glomerulonephritis
Uterine Rupture
FH
Fumarase Deficiency