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Diseases
Genes (772)
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SCN5A
Cardiac Conduction Defect
FKRP
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
SLC52A3
Brown-Vialetto-Van Laere Syndrome 1
MED12
Fg Syndrome
MFSD8
Macular Dystrophy With Central Cone Involvement
POMGNT1
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
POMT1
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
DAG1
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
FKTN
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
CRPPA
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
POMGNT2
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
B4GAT1
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
OPN1MW
Colorblindness, Partial, Deutan Series
POMT2
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
LARGE1
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
RXYLT1
Muscular Dystrophy-Dystroglycanopathy (Congenital With Brain And Eye Anomalies), Type A, 13
MSLN
Mesothelioma, Malignant
BAP1
Mesothelioma, Malignant
CDKN2A
Mesothelioma, Malignant
SLC52A2
Brown-Vialetto-Van Laere Syndrome 1
Mesothelioma, Malignant