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Diseases
Genes (916)
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PROM1
Stargardt Disease 4
Cone-Rod Dystrophy 12
Cone-Rod Dystrophy 11
Macular Dystrophy, Retinal, 2
ABCA4
Stargardt Disease 4
Cone-Rod Dystrophy 11
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
SLC40A1
Hemochromatosis Type 4
FMR1
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
PQBP1
Renpenning's Syndrome
PDGFRB
Chordoma, Susceptibility To
Primary Familial Brain Calcification
Unicameral Bone Cyst
PMM2
Pmm2 Deficiency
CRX
Pinealoblastoma
Stargardt Disease 4
Cone-Rod Dystrophy 11
SLC2A1
Glucose Transporter Type 1 Deficiency Syndrome
GALE
Guillain-Barré Syndrome
Galactose Epimerase Deficiency
SLC20A2
Primary Familial Brain Calcification
MAGEL2
Schaaf-Yang Syndrome
ZNF335
Microcephaly 10, Primary, Autosomal Recessive
FARS2
Spastic Paraplegia 77, Autosomal Recessive
PRPH2
Stargardt Disease 4
Cone-Rod Dystrophy 11
TBXT
Chordoma, Susceptibility To
DDIT3
Myxoid Liposarcoma
FUS
Myxoid Liposarcoma
GSTZ1
Maleylacetoacetate Isomerase Deficiency