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Diseases
Genes (641)
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SLC20A2
Primary Familial Brain Calcification
Basal Ganglia Disease
PDGFRB
Primary Familial Brain Calcification
Basal Ganglia Disease
ATRX
Alpha-Thalassemia Mental Retardation Syndrome
ATP7B
Wilson's Disease
COL2A1
Collagen, Type Ii, Alpha-1
MED12
Fg Syndrome
Alpha-Thalassemia Mental Retardation Syndrome
GPR143
Ocular Albinism, X-Linked
PDGFB
Callosity
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
OPN1LW
Colorblindness, Partial, Protan Series
Color Blindness
OPN1MW
Colorblindness, Partial, Deutan Series
XPR1
Primary Familial Brain Calcification
Basal Ganglia Disease
Wilson's Disease
BLVRA
Hyperbiliverdinemia
OFD1
Orofaciodigital Syndrome 1
ANXA5
Wilson's Disease
TMEM107
Orofaciodigital Syndrome 1
PRKACA
Fibrolamellar Hepatocellular Carcinoma
DNAJB1
Fibrolamellar Hepatocellular Carcinoma