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Diseases
Genes (2242)
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AR
Disinhibition
Retinoblastoma
Spinal And Bulbar Muscular Atrophy
Spinal And Bulbar Muscular Atrophy
Spinal And Bulbar Muscular Atrophy, X-Linked 1
Encephalomyelitis
GALE
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
FAM20A
Enamel-Renal Syndrome
RB1
Retinoblastoma
Pinealoblastoma
MYH7
Laing Distal Myopathy
SLC2A10
Arterial Tortuosity Syndrome
SLC26A2
Atelosteogenesis, Type Ii
GALK1
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
SLITRK1
Gilles De La Tourette Syndrome
CEBPE
Neutrophil-Specific Granule Deficiency
PCDH19
Epilepsy-Intellectual Disability In Females
HDC
Gilles De La Tourette Syndrome
NRAS
Retinoblastoma
Neurocutaneous Melanosis
SMARCD2
Neutrophil-Specific Granule Deficiency
TNF
Retinoblastoma
Gilles De La Tourette Syndrome
Spinal And Bulbar Muscular Atrophy
Sjogren Syndrome
Encephalomyelitis
PTCH1
Medulloblastoma
SMO
Medulloblastoma