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Diseases
Genes (930)
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ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
Hypertelorism
TBX5
Holt-Oram Syndrome
PEX1
Peroxisome Biogenesis Disorder 10a (Zellweger)
Hypertelorism
MED13L
Congenitally Uncorrected Transposition Of The Great Arteries
Hypertelorism
FOXE3
Aortic Aneurysm, Familial Thoracic 11, Susceptibility To
Hypertelorism
GATA2
Immunodeficiency 21
GALK1
Galactokinase Deficiency
FOXP2
Foxp2-Related Speech And Language Disorder
ADGRG1
Bilateral Frontoparietal Polymicrogyria
FOXG1
Foxg1 Syndrome
TBX19
Acth Deficiency, Isolated
FBXO7
Parkinson Disease 15, Autosomal Recessive Early-Onset
FBXL4
Mitochondrial Dna Depletion Syndrome 13 (Encephalomyopathic Type)
PEX3
Peroxisome Biogenesis Disorder 10a (Zellweger)
Hypertelorism
PEX6
Peroxisome Biogenesis Disorder 10a (Zellweger)
Hypertelorism
PEX2
Peroxisome Biogenesis Disorder 10a (Zellweger)
Hypertelorism
COX4I2
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
PEX26
Peroxisome Biogenesis Disorder 10a (Zellweger)
Hypertelorism
CFH
Membranoproliferative Glomerulonephritis