Name

EPRPDC Gene

Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp

PNKD2 Gene

paroxysmal nonkinesigenic dyskinesia 2

PNKD Gene

paroxysmal nonkinesigenic dyskinesia

This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]

CSE Gene

choreoathetosis/spasticity, episodic (paroxysmal choreoathetosis/spasticity)

paroxysmal drowsiness Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal drowsiness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

drowsiness Gene Set

From HPO Gene-Disease Associations

genes associated with the drowsiness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Paroxysmal atrial fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Paroxysmal atrial fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile convulsions and paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions and paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Paroxysmal nocturnal hemoglobinuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Paroxysmal nocturnal hemoglobinuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Paroxysmal familial ventricular fibrillation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Paroxysmal familial ventricular fibrillation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular fibrillation, paroxysmal familial, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy and paroxysmal dyskinesia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy and paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Paroxysmal Extreme Pain Disorder Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paroxysmal Extreme Pain Disorder from the curated CTD Gene-Disease Associations dataset.

Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.

Paroxysmal ventricular fibrillation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paroxysmal ventricular fibrillation from the curated CTD Gene-Disease Associations dataset.

Paroxysmal nonkinesigenic dyskinesia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paroxysmal nonkinesigenic dyskinesia from the curated CTD Gene-Disease Associations dataset.

Tachycardia, Paroxysmal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tachycardia, Paroxysmal from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy and Paroxysmal Dyskinesia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy and Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset.

Familial paroxysmal dystonia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Familial paroxysmal dystonia from the curated CTD Gene-Disease Associations dataset.

Hemoglobinuria, Paroxysmal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hemoglobinuria, Paroxysmal from the curated CTD Gene-Disease Associations dataset.

Paroxysmal Nonkinesigenic Dyskinesia 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paroxysmal Nonkinesigenic Dyskinesia 2 from the curated CTD Gene-Disease Associations dataset.

Benign Paroxysmal Positional Vertigo Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Benign Paroxysmal Positional Vertigo from the curated CTD Gene-Disease Associations dataset.

benign paroxysmal positional nystagmus Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease benign paroxysmal positional nystagmus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anemia, aplastic; aplastic anemia; hemoglobinuria, paroxysmal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, aplastic; aplastic anemia; hemoglobinuria, paroxysmal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemoglobinuria, paroxysmal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemoglobinuria, paroxysmal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

paroxysmal Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term paroxysmal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

paroxysmal atrial fibrillation Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal atrial fibrillation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal choreoathetosis Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal choreoathetosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal ventricular tachycardia Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal ventricular tachycardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal atrial tachycardia Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal atrial tachycardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal supraventricular tachycardia Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal supraventricular tachycardia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal lethargy Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal lethargy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal bursts of laughter Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal bursts of laughter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal involuntary eye movements Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal dyskinesia Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal dyskinesia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paroxysmal nocturnal hemoglobinuria Gene Set

From HPO Gene-Disease Associations

genes associated with the paroxysmal nocturnal hemoglobinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hemoglobinuria, Paroxysmal Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hemoglobinuria, Paroxysmal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

paroxysmal nonkinesigenic dyskinesia Gene Set

From OMIM Gene-Disease Associations

genes associated with the paroxysmal nonkinesigenic dyskinesia phenotype from the curated OMIM Gene-Disease Associations dataset.

generalized epilepsy and paroxysmal dyskinesia Gene Set

From OMIM Gene-Disease Associations

genes associated with the generalized epilepsy and paroxysmal dyskinesia phenotype from the curated OMIM Gene-Disease Associations dataset.

paroxysmal extreme pain disorder, 167400, Gene Set

From OMIM Gene-Disease Associations

genes associated with the paroxysmal extreme pain disorder, 167400, phenotype from the curated OMIM Gene-Disease Associations dataset.

?paroxysmal nocturnal hemoglobinuria 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?paroxysmal nocturnal hemoglobinuria 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular fibrillation, paroxysmal familial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular fibrillation, paroxysmal familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp phenotype from the curated OMIM Gene-Disease Associations dataset.

paroxysmal nonkinesigenic dyskinesia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the paroxysmal nonkinesigenic dyskinesia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

paroxysmal nocturnal hemoglobinuria, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the paroxysmal nocturnal hemoglobinuria, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

convulsions, familial infantile, with paroxysmal choreoathetosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the convulsions, familial infantile, with paroxysmal choreoathetosis phenotype from the curated OMIM Gene-Disease Associations dataset.