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Diseases
Genes (1060)
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PROM1
Stargardt Disease 4
Cone-Rod Dystrophy 12
Cone-Rod Dystrophy 11
Macular Dystrophy, Retinal, 2
MAGEL2
Schaaf-Yang Syndrome
Schaaf-Yang Syndrome
ABCA4
Stargardt Disease 4
Cone-Rod Dystrophy 11
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
SLC40A1
Hemochromatosis Type 4
SH2D1A
Lymphoproliferative Syndrome, X-Linked, 2
PRPH2
Stargardt Disease 4
Cone-Rod Dystrophy 11
Macular Dystrophy, Patterned, 1
FMR1
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Schaaf-Yang Syndrome
CEACAM16
Deafness, Autosomal Dominant 4a
Deafness, Autosomal Dominant 4b
PQBP1
Renpenning's Syndrome
PMM2
Pmm2 Deficiency
CRX
Pinealoblastoma
Stargardt Disease 4
Cone-Rod Dystrophy 11
SLC2A1
Glucose Transporter Type 1 Deficiency Syndrome
Basal-Like Carcinoma
SNRPN
Cone-Rod Dystrophy 11
Schaaf-Yang Syndrome
PDGFRB
Chordoma, Susceptibility To
Primary Familial Brain Calcification
SLC20A2
Primary Familial Brain Calcification
GALE
Galactose Epimerase Deficiency
SLC26A4
Deafness, Autosomal Recessive 4, With Enlarged Vestibular Aqueduct
MYH14
Deafness, Autosomal Dominant 4a
ZNF335
Microcephaly 10, Primary, Autosomal Recessive