FindZebra
About
Contact
Help
Login
Diseases
Genes (770)
Deep Research
Advanced
Download Gene List
NAGA
Schindler Disease, Type I
Alpha-N-Acetylgalactosaminidase Deficiency Type 3
Alpha-N-Acetylgalactosaminidase Deficiency Type 2
Infantile Neuroaxonal Dystrophy
PLA2G6
Infantile Neuroaxonal Dystrophy
ASL
Argininosuccinic Aciduria
SCN5A
Cardiac Conduction Defect
PMM2
Pmm2 Deficiency
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
CTC1
Cerebroretinal Microangiopathy With Calcifications And Cysts 1
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