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Diseases
Genes (2839)
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TEK
Glaucoma 3, Primary Congenital, E
Multiple Cutaneous And Mucosal Venous Malformations
Primary Congenital Glaucoma
Glomuvenous Malformation
Angiosarcoma
Blue Rubber Bleb Nevus Syndrome
Clear Cell Renal Carcinoma
Neovascularization
KDR
Angiosarcoma
Clear Cell Renal Carcinoma
Neovascularization
ADGRG1
Polymicrogyria
Bilateral Frontoparietal Polymicrogyria
CYP1B1
Glaucoma 3, Primary Congenital, E
Primary Congenital Glaucoma
Clear Cell Renal Carcinoma
TP53
Angiosarcoma
Clear Cell Renal Carcinoma
FMR1
Disinhibition
Fg Syndrome
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
GLMN
Glomuvenous Malformation
Blue Rubber Bleb Nevus Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
C9orf72
Disinhibition
Frontotemporal Dementia And/or Amyotrophic Lateral Sclerosis 1
Fragile X-Associated Tremor/ataxia Syndrome
LTBP2
Glaucoma 3, Primary Congenital, E
Primary Congenital Glaucoma
FLCN
Clear Cell Renal Carcinoma
SLC12A6
Andermann Syndrome
OPA3
Costeff Syndrome
PTEN
Glaucoma 3, Primary Congenital, E
Angiosarcoma
Clear Cell Renal Carcinoma
Protein Losing Enteropathy
Thrombophlebitis
Polymicrogyria
VEGFA
Angiosarcoma
Clear Cell Renal Carcinoma
Neovascularization
VHL
Angiosarcoma
Clear Cell Renal Carcinoma
MED12
Clear Cell Renal Carcinoma
Fg Syndrome
IFIH1
Glaucoma 3, Primary Congenital, E
Singleton Merten Syndrome
PQBP1
Renpenning's Syndrome
NGLY1
Ngly1 Deficiency