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Diseases
Genes (596)
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OPN1LW
Colorblindness, Partial, Protan Series
Color Blindness
Color Vision Deficiency
OPN1MW
Colorblindness, Partial, Deutan Series
Color Vision Deficiency
SLC20A2
Cyclopia
Primary Familial Brain Calcification
Basal Ganglia Disease
ATP7B
Wilson's Disease
PDGFRB
Primary Familial Brain Calcification
Basal Ganglia Disease
BEST1
Wilson's Disease
Vitelliform Macular Dystrophy
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
COL2A1
Collagen, Type Ii, Alpha-1
MED12
Fg Syndrome
Alpha-Thalassemia Mental Retardation Syndrome
GPR143
Ocular Albinism, X-Linked
PDGFB
Primary Familial Brain Calcification
Basal Ganglia Disease
TAF1
Dystonia 3, Torsion, X-Linked
MFSD8
Macular Dystrophy With Central Cone Involvement
UBA1
X-Linked Spinal Muscular Atrophy Type 2
XPR1
Wilson's Disease
Primary Familial Brain Calcification
Basal Ganglia Disease
BLVRA
Hyperbiliverdinemia
OFD1
Orofaciodigital Syndrome 1
ANXA5
Wilson's Disease
SHH
Cyclopia
TMEM107
Orofaciodigital Syndrome 1