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Diseases
Genes (412)
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KCNJ10
Generalized Tonic–clonic Seizure
Sesame Syndrome
ABHD5
Cerebral Creatine Deficiency
EFHC1
Generalized Tonic–clonic Seizure
Epilepsy, Myoclonic Juvenile
GAMT
Guanidinoacetate Methyltransferase Deficiency
WFS1
Wolfram Syndrome, Mitochondrial Form
ATCAY
Cerebellar Ataxia, Cayman Type
ST3GAL5
Gm3 Synthase Deficiency
Paroxysmal Nonkinesigenic Dyskinesia 2
NAGA
Alpha-N-Acetylgalactosaminidase Deficiency Type 1
TREX1
Vasculopathy, Retinal, With Cerebral Leukodystrophy
GABRA1
Epilepsy, Myoclonic Juvenile
PSAP
Hepatitis E
Encephalopathy Due To Prosaposin Deficiency
PNKD
Paroxysmal Nonkinesigenic Dyskinesia 2
CISD2
Wolfram Syndrome, Mitochondrial Form
CACNB4
Epilepsy, Myoclonic Juvenile
JRK
Epilepsy, Myoclonic Juvenile
MYH7
Left Ventricular Noncompaction 7
SRD5A2
Alopecia, Androgenetic, 1
MYBPC3
Left Ventricular Noncompaction 7
AR
Alopecia, Androgenetic, 1
PRRT2
Paroxysmal Nonkinesigenic Dyskinesia 2