Results for "Hyperammonemia": 25 gene sets

Name

Hyperammonemia Gene Set

From CTD Gene-Disease Associations

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

hyperammonemia Gene Set

From GeneRIF Biological Term Annotations

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

hyperammonemia Gene Set

From HPO Gene-Disease Associations

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

Hyperammonemia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hyperammonemia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hyperammonemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hyperammonemia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Hyperammonemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Hyperammonemia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hyperammonemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Carbonic anhydrase va deficiency, hyperammonemia due to Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperammonemia, type III Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperammonemia, type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperinsulinism-hyperammonemia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperinsulinism-hyperammonemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital hyperammonemia, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital hyperammonemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset.

epilepsy; hyperammonemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; hyperammonemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute neonatal disease and hyperammonemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute neonatal disease and hyperammonemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute hyperammonemia Gene Set

From HPO Gene-Disease Associations

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

asymptomatic hyperammonemia Gene Set

From HPO Gene-Disease Associations

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

hyperammonemia due to carbonic anhydrase va deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperammonemia due to carbonic anhydrase va deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperornithinemia-hyperammonemia-homocitrullinemia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperornithinemia-hyperammonemia-homocitrullinemia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperinsulinism-hyperammonemia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperinsulinism-hyperammonemia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Acute Hyperammonemia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Acute Hyperammonemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Asymptomatic Hyperammonemia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Asymptomatic Hyperammonemia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Congenital hyperammonemia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital hyperammonemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hyperinsulinism-hyperammonemia syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hyperinsulinism-hyperammonemia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.