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Results for "finnish": 17 gene sets

Name
finnish Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term finnish in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Finnish Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Finnish congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aspartylglucosaminuria, finnish type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aspartylglucosaminuria, finnish type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Finnish lethal neonatal metabolic syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Finnish lethal neonatal metabolic syndrome from the curated CTD Gene-Disease Associations dataset.
finnish type amyloidosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease finnish type amyloidosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
megaloblastic anemia-1, finnish type Gene Set From OMIM Gene-Disease Associations genes associated with the megaloblastic anemia-1, finnish type phenotype from the curated OMIM Gene-Disease Associations dataset.
amyloidosis, finnish type Gene Set From OMIM Gene-Disease Associations genes associated with the amyloidosis, finnish type phenotype from the curated OMIM Gene-Disease Associations dataset.
Sialic Acid Storage Disease, Finnish Type (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sialic Acid Storage Disease, Finnish Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Finnish Congenital Nephrotic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Finnish Congenital Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Aspartylglucosaminuria, Finnish Type Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aspartylglucosaminuria, Finnish Type in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Jk-Null Variant, Finnish Type Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Jk-Null Variant, Finnish Type in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Finnish type amyloidosis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Finnish type amyloidosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Finnish type amyloidosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Finnish type amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Finnish congenital nephrotic syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lethal congenital contractural syndrome Finnish Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lethal congenital contractural syndrome Finnish phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Finnish upper limb-onset distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish upper limb-onset distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.