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Diseases
Genes (324)
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SLC20A2
Basal Ganglia Disease
Primary Familial Brain Calcification
PDGFRB
Basal Ganglia Disease
Primary Familial Brain Calcification
SCN5A
Cardiac Conduction Defect
SLC52A3
Brown-Vialetto-Van Laere Syndrome 1
GPR143
Ocular Albinism, X-Linked
MED12
Fg Syndrome
PDGFB
Basal Ganglia Disease
Primary Familial Brain Calcification
MFSD8
Macular Dystrophy With Central Cone Involvement
FLNC
Cardiomyopathy, Familial Hypertrophic, 26
TERT
Dyskeratosis Congenita, Autosomal Recessive 5
OPN1MW
Colorblindness, Partial, Deutan Series
XPR1
Basal Ganglia Disease
Primary Familial Brain Calcification
RTEL1
Dyskeratosis Congenita, Autosomal Recessive 5
SLC52A2
Brown-Vialetto-Van Laere Syndrome 1
DKC1
Dyskeratosis Congenita, Autosomal Recessive 5
ACD
Dyskeratosis Congenita, Autosomal Recessive 5
TINF2
Dyskeratosis Congenita, Autosomal Recessive 5
PRKACA
Fibrolamellar Hepatocellular Carcinoma
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
NSMCE2
Seckel Syndrome 10