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Diseases
Genes (415)
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OPN1LW
Colorblindness, Partial, Protan Series
Color Blindness
Color Vision Deficiency
OPN1MW
Colorblindness, Partial, Deutan Series
Color Vision Deficiency
SLC20A2
Primary Familial Brain Calcification
Basal Ganglia Disease
PDGFRB
Primary Familial Brain Calcification
Basal Ganglia Disease
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
MED12
Fg Syndrome
Alpha-Thalassemia Mental Retardation Syndrome
GPR143
Ocular Albinism, X-Linked
MFSD8
Macular Dystrophy With Central Cone Involvement
GNAQ
Sturge–weber Syndrome
Color Vision Deficiency
PDGFB
Primary Familial Brain Calcification
Basal Ganglia Disease
TAF1
Dystonia 3, Torsion, X-Linked
UBA1
X-Linked Spinal Muscular Atrophy Type 2
AGGF1
Klippel-Trenaunay-Weber Syndrome
RASA1
Klippel-Trenaunay-Weber Syndrome
Sturge–weber Syndrome
XPR1
Primary Familial Brain Calcification
Basal Ganglia Disease
BLVRA
Hyperbiliverdinemia
OFD1
Orofaciodigital Syndrome 1
TMEM107
Orofaciodigital Syndrome 1
CNGA3
Color Blindness
Color Vision Deficiency
PDE6H
Color Blindness
Color Vision Deficiency