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Diseases
Genes (1264)
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SLC4A11
Congenital Hereditary Endothelial Dystrophy Type I
Posterior Polymorphous Corneal Dystrophy
Congenital Hereditary Endothelial Dystrophy Type Ii
Fuchs Endothelial Corneal Dystrophy
LMNA
Localized Scleroderma
Linear Scleroderma
Vocal Cord Paralysis
Scleroderma
Sinoatrial Block
Hypertelorism
ZEB1
Posterior Polymorphous Corneal Dystrophy
Congenital Hereditary Endothelial Dystrophy Type Ii
Fuchs Endothelial Corneal Dystrophy
PMM2
Pmm2 Deficiency
Hypertelorism
TNF
Localized Scleroderma
Linear Scleroderma
Scleroderma
Snoring
Foxp2-Related Speech And Language Disorder
Sore Throat
ASL
Argininosuccinic Aciduria
COL8A2
Congenital Hereditary Endothelial Dystrophy Type I
Posterior Polymorphous Corneal Dystrophy
Congenital Hereditary Endothelial Dystrophy Type Ii
Fuchs Endothelial Corneal Dystrophy
OVOL2
Congenital Hereditary Endothelial Dystrophy Type I
Posterior Polymorphous Corneal Dystrophy
Congenital Hereditary Endothelial Dystrophy Type Ii
Fuchs Endothelial Corneal Dystrophy
CSF3
Localized Scleroderma
Linear Scleroderma
Scleroderma
FGFR2
Mcgillivray Syndrome
Hypertelorism
FOXP2
Foxp2-Related Speech And Language Disorder
FOXG1
Foxg1 Syndrome
COX4I2
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
VSX1
Congenital Hereditary Endothelial Dystrophy Type I
Posterior Polymorphous Corneal Dystrophy
Fuchs Endothelial Corneal Dystrophy
Hypertelorism
VHL
Varicose Veins
Vocal Cord Paralysis
TCF4
Fuchs Endothelial Corneal Dystrophy
XYLT2
Scleroderma
Hypertelorism
EFNB1
Hypertelorism
TNC
Varicose Veins
Bullous Keratopathy
Scleroderma
GRHL2
Posterior Polymorphous Corneal Dystrophy