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Diseases
Genes (544)
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ABCA1
Tangier Disease
Familial Hdl Deficiency
BEST1
Vitelliform Macular Dystrophy
ABCC2
Rotor Syndrome
Dubin-Johnson Syndrome
CARD14
Pityriasis Rubra Pilaris
SLC4A1
Thalassemia
Ovalocytosis, Southeast Asian
HPRT1
Hypoxanthine Guanine Phosphoribosyltransferase Partial Deficiency
SLCO1B1
Rotor Syndrome
IKBKG
Immunodeficiency Without Anhidrotic Ectodermal Dysplasia
SLCO1B3
Rotor Syndrome
BCO1
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant
CD55
Protein Losing Enteropathy
FGF5
Trichomegaly
PRPH2
Vitelliform Macular Dystrophy
RB1
Pinealoblastoma
Trilateral Retinoblastoma
IMPG1
Vitelliform Macular Dystrophy
ALK
Inflammatory Breast Cancer
IMPG2
Vitelliform Macular Dystrophy
S100B
Fibrous Dysplasia Of Bone
Erethism
ADAM17
Immunodeficiency Without Anhidrotic Ectodermal Dysplasia
JUN
Erethism