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Diseases
Genes (567)
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SLC20A2
Basal Ganglia Disease
Primary Familial Brain Calcification
GJA1
Hippocampal Sclerosis
Neurodegeneration With Brain Iron Accumulation
Oculodentodigital Dysplasia
PDGFRB
Basal Ganglia Disease
Primary Familial Brain Calcification
GPR143
Ocular Albinism, X-Linked
PDGFB
Basal Ganglia Disease
Primary Familial Brain Calcification
MED12
Fg Syndrome
MFSD8
Macular Dystrophy With Central Cone Involvement
ACSF3
Combined Malonic And Methylmalonic Aciduria
FLNC
Cardiomyopathy, Familial Hypertrophic, 26
KDR
Infantile Hemangioma
FLT4
Infantile Hemangioma
ANTXR1
Infantile Hemangioma
CRH
Pituitary Adenoma 4, Acth-Secreting
XPR1
Basal Ganglia Disease
Primary Familial Brain Calcification
WDR45
Neurodegeneration With Brain Iron Accumulation
NRAS
Neurocutaneous Melanosis
DRD2
Basal Ganglia Disease
Pituitary Adenoma 4, Acth-Secreting
CTNS
Cystinosis
PRKACA
Pituitary Adenoma 4, Acth-Secreting
Fibrolamellar Hepatocellular Carcinoma
PRKAR1A
Pituitary Adenoma 4, Acth-Secreting
Fibrolamellar Hepatocellular Carcinoma