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Diseases
Genes (1239)
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ABCA1
Tangier Disease
Familial Hdl Deficiency
BEST1
Vitelliform Macular Dystrophy
UGT1A1
Crigler-Najjar Syndrome
ABCC2
Rotor Syndrome
Dubin-Johnson Syndrome
RB1
Pinealoblastoma
Leukocoria
Retinoblastoma
CARD14
Pityriasis Rubra Pilaris
SLC4A1
Ovalocytosis, Southeast Asian
HPRT1
Hypoxanthine Guanine Phosphoribosyltransferase Partial Deficiency
SLCO1B1
Rotor Syndrome
IKBKG
Immunodeficiency Without Anhidrotic Ectodermal Dysplasia
SLCO1B3
Leptospirosis
Rotor Syndrome
BCO1
Hypercarotenemia And Vitamin A Deficiency, Autosomal Dominant
CD55
Protein Losing Enteropathy
PRPH2
Vitelliform Macular Dystrophy
MDM4
Retinoblastoma
IMPG1
Vitelliform Macular Dystrophy
ALK
Inflammatory Breast Cancer
Retinoblastoma
S100B
Fibrous Dysplasia Of Bone
Leptospirosis
Erethism
IMPG2
Vitelliform Macular Dystrophy
PTEN
Inflammatory Breast Cancer
Thrombophlebitis
Retinoblastoma
Protein Losing Enteropathy