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Diseases
Genes (439)
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GRIN2A
Rolandic Epilepsy
Landau-Kleffner Syndrome
Epilepsy Syndromes
ABHD5
Cerebral Creatine Deficiency
COL1A1
Osteogenesis Imperfecta
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
COL1A2
Osteogenesis Imperfecta
GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
STX3
Microvillus Inclusion Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Placental Site Trophoblastic Tumor
Alopecia, Androgenetic, 1
GABRG2
Rolandic Epilepsy
Epilepsy Syndromes
MRAP
Familial Glucocorticoid Deficiency
GALE
Galactose-1-Phosphate Uridylyltransferase Deficiency
GALK1
Galactose-1-Phosphate Uridylyltransferase Deficiency
SRPX2
Rolandic Epilepsy
SPARC
Osteogenesis Imperfecta
Galactose-1-Phosphate Uridylyltransferase Deficiency
ABCC2
Alopecia, Androgenetic, 1
SUPV3L1
Alopecia, Androgenetic, 1