Spinal Muscular Atrophies Of Childhood

Clear Filter

Results for "Spinal Muscular Atrophies Of Childhood": 1004 gene sets

Name
Spinal Muscular Atrophies of Childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophies of Childhood from the curated CTD Gene-Disease Associations dataset.
spinal muscular atrophies of childhood Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophies of childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Spinal Muscular Atrophies of Childhood Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Muscular Atrophies of Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spinal Muscular Atrophies Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophies Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Childhood spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant childhood-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Optic Atrophies, Hereditary Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophies, Hereditary from the curated CTD Gene-Disease Associations dataset.
cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophies Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term atrophies in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Olivopontocerebellar Atrophies Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Olivopontocerebellar Atrophies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophies, Hereditary Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophies, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Severe autosomal recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Childhood Autosomal Recessive Muscular Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Childhood Autosomal Recessive Muscular Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
spinal canal and spinal cord meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal canal and spinal cord meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal cord compression; spinal osteophytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal cord compression; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Spinal Cord Injury_CNS - Spinal Cord (MMHCC)_GSE16710 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Spinal Cord Injury_CNS - Spinal Cord (MMHCC)_GSE16710 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
Spinal canal and spinal cord meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal canal and spinal cord meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, X-linked 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, autosomal recessive 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, Jerash type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy with respiratory distress 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset.
Muscular Atrophy, Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinal muscular atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
adult spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
juvenile spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intermediate spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
survival motor neuron spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular atrophy, spinal Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy phenotype Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the spinal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Muscular Atrophy, Spinal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, x-linked 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-2 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, chronic distal, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, jokela type Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset.
scapuloperoneal spinal muscular atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, late-onset, finkel type Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset.
{spinal muscular atrophy, type iii, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, lower extremity-predominant 1, ad Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, lower extremity-predominant, 2, ad Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, x-linked 3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal and bulbar muscular atrophy of kennedy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, congenital nonprogressive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.
Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Infantile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Infantile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oculopharyngeal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oculopharyngeal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Scapuloperoneal Form Of Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Form Of Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spinal muscular atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked spinal muscular atrophy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked spinal muscular atrophy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with lower extremity predominant from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with progressive myoclonic epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Adult spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Scapuloperoneal spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Scapuloperoneal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with progressive myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with lower extremity predominant in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intermediate spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked distal spinal muscular atrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked distal spinal muscular atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinal muscular atrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinal muscular atrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant adult-onset proximal spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant adult-onset proximal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy, Jokela type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy, Jokela type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy type 0 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy type 0 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with lower extremity predominant 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Adult-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Scapuloperoneal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapuloperoneal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy-progressive myoclonic epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset X-linked spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset X-linked spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
becker muscular dystrophy; duchenne muscular dystrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease becker muscular dystrophy; duchenne muscular dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular dystrophies; muscular dystrophies, limb-girdle Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular dystrophies; muscular dystrophies, limb-girdle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
North american indian childhood cirrhosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the North american indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epileptic encephalopathy, childhood-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epileptic encephalopathy, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alternating hemiplegia of childhood Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alternating hemiplegia of childhood phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypercalciuria, childhood, self-limiting Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypercalciuria, childhood, self-limiting phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Childhood hypophosphatasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Childhood hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, reducing body, X-linked, childhood-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Alternating hemiplegia of childhood 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Alternating hemiplegia of childhood 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset.
North American Indian Childhood Cirrhosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease North American Indian Childhood Cirrhosis from the curated CTD Gene-Disease Associations dataset.
Mental Disorders Diagnosed in Childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Disorders Diagnosed in Childhood from the curated CTD Gene-Disease Associations dataset.
Alternating hemiplegia of childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Alternating hemiplegia of childhood from the curated CTD Gene-Disease Associations dataset.
Arthropathy, progressive pseudorheumatoid, of childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthropathy, progressive pseudorheumatoid, of childhood from the curated CTD Gene-Disease Associations dataset.
Hypophosphatasia, Childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatasia, Childhood from the curated CTD Gene-Disease Associations dataset.
alternating hemiplegia of childhood Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease alternating hemiplegia of childhood from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
childhood medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood oligodendroglioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood type dermatomyositis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood type dermatomyositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood kidney neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood kidney neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood disintegrative disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood disintegrative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood malignant schwannoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood kidney cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood kidney cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood endodermal sinus tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alternating hemiplegia of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alternating hemiplegia of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
childhood pilocytic astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease childhood pilocytic astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
severe childhood thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease severe childhood thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood leukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood b-cell non-hodgkin's lymphoma Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood b-cell non-hodgkin's lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute lymphoblastic leukemia (childhood) Gene Set From GAD Gene-Disease Associations genes associated with the disease acute lymphoblastic leukemia (childhood) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood obesity Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchial asthma (childhood only) Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchial asthma (childhood only) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temperament in early childhood Gene Set From GAD Gene-Disease Associations genes associated with the disease temperament in early childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; periodontitis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood absence epilepsy. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood absence epilepsy. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood b-cell precursor acute lymphoblastic leukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood b-cell precursor acute lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; autoimmune diseases; celiac disease; chronic childhood arthritis; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood brain tumors ; residential insecticide exposure Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood brain tumors ; residential insecticide exposure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bronchial asthma (childhood & adult) Gene Set From GAD Gene-Disease Associations genes associated with the disease bronchial asthma (childhood & adult) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood atopic asthma Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood atopic asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; chronic childhood arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood brain tumor Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood brain tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, childhood acute lymphoblastic Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, childhood acute lymphoblastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood acute lymphoblastic leukemia Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood acute lymphoblastic leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood-onset mood disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood-onset mood disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood maltreatment Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood maltreatment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood asthma. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood asthma. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma (childhood) Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma (childhood) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leukemia, childhood acute; hypertension Gene Set From GAD Gene-Disease Associations genes associated with the disease leukemia, childhood acute; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood idiopathic thrombocytopenic purpura. Gene Set From GAD Gene-Disease Associations genes associated with the disease childhood idiopathic thrombocytopenic purpura. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma and ige in childhood Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma and ige in childhood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, rheumatoid; chronic childhood arthritis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; arthritis, psoriatic; chronic childhood arthritis; psoriatic arthropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, juvenile rheumatoid; chronic childhood arthritis; familial mediterranean fever; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
asthma (childhood onset) Gene Set From GAD Gene-Disease Associations genes associated with the disease asthma (childhood onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
childhood Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term childhood in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Fractional exhaled nitric oxide (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Fractional exhaled nitric oxide (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma (childhood onset) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Acute lymphoblastic leukemia (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Acute lymphoblastic leukemia (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Intelligence (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Intelligence (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Asthma (childhood, severe) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Asthma (childhood, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
childhood-onset short-trunk short stature Gene Set From HPO Gene-Disease Associations genes associated with the childhood-onset short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
childhood onset Gene Set From HPO Gene-Disease Associations genes associated with the childhood onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
recurrent infections in infancy and early childhood Gene Set From HPO Gene-Disease Associations genes associated with the recurrent infections in infancy and early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
death in childhood Gene Set From HPO Gene-Disease Associations genes associated with the death in childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
childhood-onset truncal obesity Gene Set From HPO Gene-Disease Associations genes associated with the childhood-onset truncal obesity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
childhood onset short-limb short stature Gene Set From HPO Gene-Disease Associations genes associated with the childhood onset short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
childhood onset sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the childhood onset sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
loss of ability to walk in early childhood Gene Set From HPO Gene-Disease Associations genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
inability to walk by childhood/adolescence Gene Set From HPO Gene-Disease Associations genes associated with the inability to walk by childhood/adolescence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
platyspondyly (childhood) Gene Set From HPO Gene-Disease Associations genes associated with the platyspondyly (childhood) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Lead Poisoning, Nervous System, Childhood Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Lead Poisoning, Nervous System, Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Schizophrenia, Childhood Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Schizophrenia, Childhood phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
hypophosphatasia, childhood Gene Set From OMIM Gene-Disease Associations genes associated with the hypophosphatasia, childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
hepatocellular carcinoma, childhood type Gene Set From OMIM Gene-Disease Associations genes associated with the hepatocellular carcinoma, childhood type phenotype from the curated OMIM Gene-Disease Associations dataset.
alternating hemiplegia of childhood 2 Gene Set From OMIM Gene-Disease Associations genes associated with the alternating hemiplegia of childhood 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, childhood absence, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, childhood absence, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
transient erythroblastopenia of childhood Gene Set From OMIM Gene-Disease Associations genes associated with the transient erythroblastopenia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 6} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, reducing body, x-linked, childhood-onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, reducing body, x-linked, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
cirrhosis, north american indian childhood type Gene Set From OMIM Gene-Disease Associations genes associated with the cirrhosis, north american indian childhood type phenotype from the curated OMIM Gene-Disease Associations dataset.
alternating hemiplegia of childhood Gene Set From OMIM Gene-Disease Associations genes associated with the alternating hemiplegia of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
arthropathy, progressive pseudorheumatoid, of childhood Gene Set From OMIM Gene-Disease Associations genes associated with the arthropathy, progressive pseudorheumatoid, of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
polyarteritis nodosa, childhood-onset Gene Set From OMIM Gene-Disease Associations genes associated with the polyarteritis nodosa, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
?neurodegeneration with optic atrophy, childhood onset Gene Set From OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset.
{epilepsy, childhood absence, susceptibility to, 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {epilepsy, childhood absence, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
epileptic encephalopathy, childhood-onset Gene Set From OMIM Gene-Disease Associations genes associated with the epileptic encephalopathy, childhood-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
Childhood Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Liposarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Liposarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Osteosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Osteosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Neuroblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Neuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Kidney Wilms Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Kidney Wilms Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Myelodysplastic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Cytopenia Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Cytopenia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Myeloid Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Absence Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Absence Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Megakaryoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Megakaryoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Alveolar Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Alveolar Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Alveolar Soft Part Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Alveolar Soft Part Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Diffuse Large Cell Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diffuse Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Hepatocellular Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Nephrotic Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nephrotic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Non-Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Non-Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pilocytic Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pilocytic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Soft Tissue Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Synovial Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Synovial Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood T Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood T Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Newly Diagnosed Childhood Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Newly Diagnosed Childhood Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Metastatic Childhood Soft Tissue Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Metastatic Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Steroid Resistant Nephrotic Syndrome Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Steroid Resistant Nephrotic Syndrome Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Burkitt Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Burkitt Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Undifferentiated Pleomorphic Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Undifferentiated Pleomorphic Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Childhood Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Childhood Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Supratentorial Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Supratentorial Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Brain Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Renal Cell Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Renal Cell Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Monocytic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Monocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Myelomonocytic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myelomonocytic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood B Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood B Acute Lymphoblastic Leukemia With T(9;22)(Q34.1;Q11.2); Bcr-Abl1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Acute Lymphoblastic Leukemia With T(9;22)(Q34.1;Q11.2); Bcr-Abl1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Burkitt Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Burkitt Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Chronic Myelogenous Leukemia, Bcr-Abl1 Positive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Chronic Myelogenous Leukemia, Bcr-Abl1 Positive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Hematopoietic Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hematopoietic Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pre-B Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pre-B Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Oligodendroglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Oligodendroglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ataxia With Central Nervous System Hypomyelinization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ataxia With Central Nervous System Hypomyelinization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Brain Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Craniopharyngioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Craniopharyngioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Eosinophilic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Eosinophilic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Embryonal Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Embryonal Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ganglioneuroblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ganglioneuroblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Leiomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Leiomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polyarteritis Nodosa, Childhood-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polyarteritis Nodosa, Childhood-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Brain Stem Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Stem Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Cerebral Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebral Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Anaplastic Large Cell Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Malignant Peripheral Nerve Sheath Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Peripheral Nerve Sheath Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Gliosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gliosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Indian Childhood Cirrhosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Indian Childhood Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Angiosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Angiosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alternating Hemiplegia Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Testicular Germ Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Testicular Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ganglioglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ganglioglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Germ Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Teratoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Teratoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Lymphoblastic Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Childhood Caries Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Caries in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Promyelocytic Leukemia With Pml-Rara Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Promyelocytic Leukemia With Pml-Rara in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pleomorphic Xanthoastrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pleomorphic Xanthoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Childhood Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood T Lymphoblastic Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood T Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Epithelioid Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Epithelioid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Onset Dystonias Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Onset Dystonias in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Large Cell Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Large Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Hypophosphatasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Hypophosphatasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Childhood Hepatocellular Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Hepatocellular Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Subependymal Giant Cell Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Subependymal Giant Cell Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Anaplastic Oligoastrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Oligoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Anaplastic Oligodendroglioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Oligodendroglioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Grade I Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade I Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Langerhans Cell Histiocytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Langerhans Cell Histiocytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Atopic Dermatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Atopic Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Childhood Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Refractory Childhood Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Refractory Childhood Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pineoblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pineoblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Nasal Type Extranodal Nk/T-Cell Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nasal Type Extranodal Nk/T-Cell Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Monoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Monoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Clear Cell Sarcoma Of Soft Parts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Clear Cell Sarcoma Of Soft Parts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Immunoblastic Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Immunoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alternating Hemiplegia Of Childhood 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alternating Hemiplegia Of Childhood 2 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alternating Hemiplegia Of Childhood 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Diffuse Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diffuse Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Oligoastrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Oligoastrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pilomyxoid Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pilomyxoid Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Giant Cell Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Giant Cell Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Fibrillary Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Fibrillary Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood B Lymphoblastic Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood B Lymphoblastic Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Desmoplastic Small Round Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Desmoplastic Small Round Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Kidney Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Kidney Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Childhood Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Atypical Teratoid/Rhabdoid Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Atypical Teratoid/Rhabdoid Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Brain Stem Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Stem Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Gliomatosis Cerebri Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gliomatosis Cerebri in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Thyroid Gland Papillary Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Thyroid Gland Papillary Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Ovarian Germ Cell Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Ovarian Germ Cell Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Anaplastic Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Anaplastic Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Epithelioid Hemangioendothelioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Epithelioid Hemangioendothelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Brain Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Brain Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Childhood Hemangiopericytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Hemangiopericytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Pleomorphic Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Pleomorphic Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood L2 Acute Lymphoblastic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood L2 Acute Lymphoblastic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Childhood Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Malignant Solid Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Melanoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Mesenchymal Chondrosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Mesenchymal Chondrosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Erythroid Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Erythroid Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Malignant Liver Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Liver Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontal Epilepsy, Benign, Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontal Epilepsy, Benign, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
North American Indian Childhood Cirrhosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease North American Indian Childhood Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypercalciuria, Childhood, Self-Limiting Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypercalciuria, Childhood, Self-Limiting in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Transient Erythroblastopenia Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Transient Erythroblastopenia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Necrotizing Encephalopathy Of Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Necrotizing Encephalopathy Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Basophilic Leukemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Basophilic Leukemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Myeloid Leukemia In Remission Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia In Remission in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Nodular Sclerosis Classic Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Nodular Sclerosis Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Botryoid-Type Embryonal Rhabdomyosarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Botryoid-Type Embryonal Rhabdomyosarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Central Nervous System Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Tic Disorders Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Tic Disorders in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Psychosis, Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Psychosis, Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Bronchiectasis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Bronchiectasis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1A, Severe, With Infantile Or Early Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reducing Body Myopathy, X-Linked 1B, With Late Childhood Or Adult Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Onset Of Psoriasis In Childhood (1-10 Years) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Onset Of Psoriasis In Childhood (1-10 Years) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Conduct Disorder, Childhood-Onset Type Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Conduct Disorder, Childhood-Onset Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Gemistocytic Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gemistocytic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood-Onset Spasticity With Hyperglycinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood-Onset Spasticity With Hyperglycinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorea, Childhood-Onset, With Psychomotor Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorea, Childhood-Onset, With Psychomotor Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Celiac Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Celiac Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Diabetes Mellitus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Diabetes Mellitus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Malignant Childhood Central Nervous System Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Malignant Childhood Central Nervous System Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Grade Ii Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade Ii Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Benign Focal Epilepsy, Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Benign Focal Epilepsy, Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Benign Occipital Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Benign Occipital Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Metastatic Childhood Soft Tissue Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Metastatic Childhood Soft Tissue Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Gastrointestinal Stromal Tumor Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Gastrointestinal Stromal Tumor in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progeria Syndrome, Childhood-Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progeria Syndrome, Childhood-Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Malignant Fibrous Histiocytoma Of Bone Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Malignant Fibrous Histiocytoma Of Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Recurrent Childhood Anaplastic Astrocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Childhood Anaplastic Astrocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Small Intestinal Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Small Intestinal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Colorectal Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Colorectal Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Thyroid Gland Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Thyroid Gland Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Grade Iii Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Grade Iii Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Mixed Glioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Mixed Glioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Myeloid Leukemia/Other Myeloid Malignancies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early Childhood Epilepsy, Myoclonic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Early Childhood Epilepsy, Myoclonic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Supratentorial Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Supratentorial Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early Childhood Onset Retinal Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early Childhood Onset Retinal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sudden Unexplained Death In Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sudden Unexplained Death In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Acute Leukemia In Remission Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Acute Leukemia In Remission in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Infratentorial Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Infratentorial Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Disintegrative Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Disintegrative Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Progressive Bulbar Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Progressive Bulbar Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Depression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pneumonia Childhood Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pneumonia Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Choroid Plexus Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Choroid Plexus Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood-Onset Short-Trunk Short Stature Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood-Onset Short-Trunk Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Cerebellar Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebellar Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Onset Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Death In Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Death In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Solid Neoplasm Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Solid Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood-Onset Truncal Obesity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood-Onset Truncal Obesity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Overweight Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Overweight in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Aggression Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Aggression in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tongue Thrusting When Swallowing, Abnormal Persistence Beyond Early Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tongue Thrusting When Swallowing, Abnormal Persistence Beyond Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Selective Mutism Specific To Childhood And Adolescence Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Selective Mutism Specific To Childhood And Adolescence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Recurrent Infections In Infancy And Early Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Infections In Infancy And Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Loss Of Ability To Walk In Early Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Ability To Walk In Early Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Onset Short-Limb Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset Short-Limb Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Convulsion In Childhood Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Convulsion In Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Inability To Walk By Childhood/Adolescence Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Inability To Walk By Childhood/Adolescence in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood Onset Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Childhood Onset Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Childhood electroclinical syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood electroclinical syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Childhood absence epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Childhood absence epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Alternating hemiplegia of childhood Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Alternating hemiplegia of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive pseudorheumatoid arthropathy of childhood Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive pseudorheumatoid arthropathy of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Childhood type dermatomyositis Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Childhood type dermatomyositis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood acute lymphocytic leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute lymphocytic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood endodermal sinus tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood endodermal sinus tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood electroclinical syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood electroclinical syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood B-cell acute lymphoblastic leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood B-cell acute lymphoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood fibrosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood fibrosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood low-grade glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood low-grade glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood kidney cell carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood absence epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood disintegrative disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood disintegrative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood acute myeloid leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute myeloid leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood kidney cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood type dermatomyositis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood type dermatomyositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood malignant schwannoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood malignant schwannoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Systemic Epstein-Barr virus positive T-cell lymphoma of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Systemic Epstein-Barr virus positive T-cell lymphoma of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood T-cell acute lymphoblastic leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood T-cell acute lymphoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood brain stem neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood brain stem neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood brain stem glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood brain stem glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood osteosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood osteosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood germ cell cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood germ cell cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood astrocytic tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood astrocytic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood infratentorial ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood infratentorial ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood leptomeningeal melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood leptomeningeal melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood angiosarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood angiosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood pilocytic astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood pilocytic astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Alternating hemiplegia of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alternating hemiplegia of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 28, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 28, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
stress-induced childhood-onset neurodegeneration with variable ataxia and seizures Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease stress-induced childhood-onset neurodegeneration with variable ataxia and seizures in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood hypophosphatasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood hypophosphatasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset neurodegeneration with brain atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset neurodegeneration with brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset dystonia with optic atrophy and basal ganglia abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood central nervous system embryonal tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood central nervous system embryonal tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood hepatocellular carcinoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood hepatocellular carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood oligodendroglioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood acute megakaryoblastic leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood acute megakaryoblastic leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dystonia 35, childhood-onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dystonia 35, childhood-onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive pseudorheumatoid arthropathy of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive pseudorheumatoid arthropathy of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood liposarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood liposarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood supratentorial ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood supratentorial ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood testicular germ cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood testicular germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Malignant childhood germ cell neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Malignant childhood germ cell neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood infratentorial neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood infratentorial neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood optic nerve glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood optic nerve glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood kidney angiomyolipoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood kidney angiomyolipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood ovarian dysgerminoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ovarian dysgerminoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood ovarian germ cell tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood ovarian germ cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood onset hearing loss Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood apraxia of speech Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood apraxia of speech phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe early-childhood-onset retinal dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe early-childhood-onset retinal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Glaucoma of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Glaucoma of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alternating hemiplegia of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Alternating hemiplegia of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood hypophosphatasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood hypophosphatasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood onset GLUT1 deficiency syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset GLUT1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood encephalopathy due to thiamine pyrophosphokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood neoplasm Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood neoplasm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe underweight in infancy childhood and adolescence Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe underweight in infancy childhood and adolescence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood ganglioglioma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood ganglioglioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood myocerebrohepatopathy spectrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood myocerebrohepatopathy spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive bulbar palsy of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive bulbar palsy of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood Onset Dystonias Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood Onset Dystonias phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood kidney cell carcinoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood kidney cell carcinoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive childhood encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive childhood encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood-onset motor and cognitive regression syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset motor and cognitive regression syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile or childhood onset neurodegenerative disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile or childhood onset neurodegenerative disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood absence epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary North American Indian childhood cirrhosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary North American Indian childhood cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Death in childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Death in childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sudden unexplained death in childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sudden unexplained death in childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood-onset autosomal recessive myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood-onset autosomal recessive myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
B-cell childhood acute lymphoblastic leukemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the B-cell childhood acute lymphoblastic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood onset sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood onset sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood Onset VCP-related Neurodevelopmental Disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Childhood Onset VCP-related Neurodevelopmental Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Disabling pansclerotic morphea of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Disabling pansclerotic morphea of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Benign childhood epilepsy with centro-temporal spikes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Benign childhood epilepsy with centro-temporal spikes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cutaneous mastocytosis (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cutaneous mastocytosis (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
First fracture in long-term childhood cancer survivors (time to event) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the First fracture in long-term childhood cancer survivors (time to event) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood body mass index Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood body mass index phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anthracycline-induced cardiotoxicity in childhood cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anthracycline-induced cardiotoxicity in childhood cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obesity in adult survivors of childhood cancer exposed to cranial radiation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obesity in adult survivors of childhood cancer exposed to cranial radiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obesity in adult survivors of childhood cancer not exposed to cranial radiation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obesity in adult survivors of childhood cancer not exposed to cranial radiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early childhood aggressive behavior Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early childhood aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Middle childhood and early adolescence aggressive behavior Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Middle childhood and early adolescence aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood and early adolescence aggressive behavior Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood and early adolescence aggressive behavior phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood ear infection Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood ear infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood maltreatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood maltreatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Meningococcal C functional antibody titers post childhood immunization Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Meningococcal C functional antibody titers post childhood immunization phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood asthma exacerbations in long-acting beta2-agonist treatment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma exacerbations in long-acting beta2-agonist treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (childhood onset) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (childhood onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma onset (childhood vs adult) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma onset (childhood vs adult) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood onset ulcerative colitis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood onset ulcerative colitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Acute lymphoblastic leukemia (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fractional exhaled nitric oxide (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fractional exhaled nitric oxide (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Fasting plasma glucose (childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Fasting plasma glucose (childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (time to childhood onset) in early life tobacco smoke exposure Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) in early life tobacco smoke exposure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Asthma (time to childhood onset) x early life tobacco smoke interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Asthma (time to childhood onset) x early life tobacco smoke interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood onset type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood onset type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood asthma with severe exacerbations Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood asthma with severe exacerbations phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Acute lymphoblastic leukemia in childhood (B cell precursor) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia in childhood (B cell precursor) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Premature menopause in childhood cancer survivors Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Premature menopause in childhood cancer survivors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood steroid-sensitive nephrotic syndrome Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood steroid-sensitive nephrotic syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to placebo treatment in childhood asthma (FVC change) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to placebo treatment in childhood asthma (FVC change) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Self-reported childhood asthma in adult smokers Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Self-reported childhood asthma in adult smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Acute lymphoblastic leukemia (adult vs childhood) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Acute lymphoblastic leukemia (adult vs childhood) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Severe exacerbations in childhood asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe exacerbations in childhood asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Breast cancer in childhood cancer survivors Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast cancer in childhood cancer survivors phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood dental caries in primary teeth Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood dental caries in primary teeth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood dental caries in permanent teeth Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood dental caries in permanent teeth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Childhood absence epilepsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Childhood absence epilepsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cisplatin-induced hearing loss in childhood cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cisplatin-induced hearing loss in childhood cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
spinal trigeminal nucleus, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in spinal trigeminal nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
spinal trigeminal nucleus, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in spinal trigeminal nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
r8 part of spinal trigeminal nucleus, interpolar part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r8 part of spinal trigeminal nucleus, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r9 part of spinal trigeminal nucleus, interpolar part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r9 part of spinal trigeminal nucleus, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r6 part of spinal vestibular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r6 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal nucleus of the trigeminal, oral part, rostral dorsomedial part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal nucleus of the trigeminal, oral part, rostral dorsomedial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r10 part of spinal trigeminal nucleus, caudal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r10 part of spinal trigeminal nucleus, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r6 part of spinal trigeminal nucleus, pars oralis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r6 part of spinal trigeminal nucleus, pars oralis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r3 part of spinal trigeminal sensory column, oral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r3 part of spinal trigeminal sensory column, oral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r10 part of spinal vestibular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r10 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r7 part of spinal vestibular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r7 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, dorsal zone Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, dorsal zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal vestibular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r11 part of spinal trigeminal nucleus, caudal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r11 part of spinal trigeminal nucleus, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r5 part of spinal vestibular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r5 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r7 part of spinal trigeminal nucleus, interpolar part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r7 part of spinal trigeminal nucleus, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r8 part of spinal vestibular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r8 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal nucleus of the trigeminal, caudal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal nucleus of the trigeminal, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal nucleus of the trigeminal, oral part, caudal dorsomedial part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal nucleus of the trigeminal, oral part, caudal dorsomedial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal nucleus of the trigeminal, interpolar part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal nucleus of the trigeminal, interpolar part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal nucleus of the trigeminal, oral part, ventrolateral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal nucleus of the trigeminal, oral part, ventrolateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r9 part of spinal vestibular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r9 part of spinal vestibular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, ventral zone Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal nucleus of the trigeminal, oral part, middle dorsomedial part, ventral zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal nucleus of the trigeminal, oral part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal nucleus of the trigeminal, oral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
spinal trigeminal nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in spinal trigeminal nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
spinal (inferior) vestibular nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in spinal (inferior) vestibular nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Neurofibromatosis, familial spinal Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neurofibromatosis, familial spinal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.
Spinal Curvatures Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Curvatures from the curated CTD Gene-Disease Associations dataset.
Spinal Dysraphism Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Dysraphism from the curated CTD Gene-Disease Associations dataset.
Spinal Cord Injuries Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Cord Injuries from the curated CTD Gene-Disease Associations dataset.
Spinal Cord Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Cord Diseases from the curated CTD Gene-Disease Associations dataset.
Spinal Cord Ischemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Cord Ischemia from the curated CTD Gene-Disease Associations dataset.
Neurofibromatosis, Familial Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neurofibromatosis, Familial Spinal from the curated CTD Gene-Disease Associations dataset.
Spinal Cord Compression Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Cord Compression from the curated CTD Gene-Disease Associations dataset.
Hematoma, Epidural, Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hematoma, Epidural, Spinal from the curated CTD Gene-Disease Associations dataset.
spinal cord glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal cord glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior spinal artery syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior spinal artery syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal cord astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal cord astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tethered spinal cord syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tethered spinal cord syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal cord disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal cord disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal cord ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal cord ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal cord melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal cord melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal cord lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal cord lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal chordoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal chordoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal canal intradural extramedullary neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal canal intradural extramedullary neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal cord oligodendroglioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal cord oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal cord primitive neuroectodermal neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal cord primitive neuroectodermal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
H3K4me3_astrocyte of the spinal cord_hg19_2 Gene Set From ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_astrocyte of the spinal cord_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.
H3K4me3_astrocyte of the spinal cord_hg19_1 Gene Set From ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_astrocyte of the spinal cord_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.
CTCF_astrocyte of the spinal cord_hg19_1 Gene Set From ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_astrocyte of the spinal cord_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.
CTCF_astrocyte of the spinal cord_hg19_2 Gene Set From ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_astrocyte of the spinal cord_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.
htlv-i infections; paraparesis, tropical spastic; spinal cord diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-i infections; paraparesis, tropical spastic; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
tuberculosis, spinal Gene Set From GAD Gene-Disease Associations genes associated with the disease tuberculosis, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acute traumatic spinal cord injury Gene Set From GAD Gene-Disease Associations genes associated with the disease acute traumatic spinal cord injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ache, low back; intervertebral disk displacement; spinal osteophytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease ache, low back; intervertebral disk displacement; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal cord injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal bone mineral density Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; spinal dysraphism Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal dysraphism Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
osteoporosis, postmenopausal; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal cord diseases; spondylosis Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal cord diseases; spondylosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal cord infarction and recurrent venous thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal cord infarction and recurrent venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
acoustic neurofibromatosis; meningioma; neurofibromatosis 2; spinal neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease acoustic neurofibromatosis; meningioma; neurofibromatosis 2; spinal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism Gene Set From GAD Gene-Disease Associations genes associated with the disease anencephaly; folic acid deficiency; neural tube defects; pregnancy complications; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fractures, bone; osteoporosis; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, bone; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ache, low back; low back pain; scoliosis; spinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease ache, low back; low back pain; scoliosis; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal ossification Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal ossification in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fractures, spontaneous; osteoporosis; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, spontaneous; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
paralysis; sensation disorders; spinal cord injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease paralysis; sensation disorders; spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
glucose metabolism disorders; obesity; spinal dysraphism Gene Set From GAD Gene-Disease Associations genes associated with the disease glucose metabolism disorders; obesity; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
osteoporosis; osteoporosis, postmenopausal; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease osteoporosis; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
htlv-i infections; spinal cord diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease htlv-i infections; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal disc degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal disc degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
femoral neck fractures; osteoporosis; spinal injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease femoral neck fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain hypoxia; burns; hypoxia, brain; spinal cord injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease brain hypoxia; burns; hypoxia, brain; spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cushing syndrome; fractures, bone; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease cushing syndrome; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
birth weight; spinal osteophytosis Gene Set From GAD Gene-Disease Associations genes associated with the disease birth weight; spinal osteophytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
osteoporosis; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
meningomyelocele; spinal dysraphism Gene Set From GAD Gene-Disease Associations genes associated with the disease meningomyelocele; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fractures, bone; hip fractures; osteoporosis; spinal injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, bone; hip fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
heart defects, congenital; spinal dysraphism Gene Set From GAD Gene-Disease Associations genes associated with the disease heart defects, congenital; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
body weight; spinal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease body weight; spinal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
arthritis, rheumatoid; fractures, bone; spinal fractures Gene Set From GAD Gene-Disease Associations genes associated with the disease arthritis, rheumatoid; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neural tube defects; spinal dysraphism Gene Set From GAD Gene-Disease Associations genes associated with the disease neural tube defects; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term spinal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Neurological pain disorder_CNS - Spinal Cord (MMHCC)_GSE18803 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Neurological pain disorder_CNS - Spinal Cord (MMHCC)_GSE18803 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
smoothened signaling pathway involved in spinal cord motor neuron cell fate specification Gene Set From GO Biological Process Annotations 2015 genes participating in the smoothened signaling pathway involved in spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord patterning Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord patterning biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord ventral commissure morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord ventral commissure morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
ventral spinal cord interneuron specification Gene Set From GO Biological Process Annotations 2015 genes participating in the ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations 2015 dataset.
ventral spinal cord development Gene Set From GO Biological Process Annotations 2015 genes participating in the ventral spinal cord development biological process from the curated GO Biological Process Annotations 2015 dataset.
smoothened signaling pathway involved in ventral spinal cord patterning Gene Set From GO Biological Process Annotations 2015 genes participating in the smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription from rna polymerase ii promoter involved in spinal cord motor neuron fate specification Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter involved in spinal cord motor neuron fate specification biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations 2015 dataset.
commissural neuron differentiation in spinal cord Gene Set From GO Biological Process Annotations 2015 genes participating in the commissural neuron differentiation in spinal cord biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord motor neuron cell fate specification Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2015 dataset.
smoothened signaling pathway involved in ventral spinal cord interneuron specification Gene Set From GO Biological Process Annotations 2015 genes participating in the smoothened signaling pathway involved in ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord association neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord association neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription from rna polymerase ii promoter involved in ventral spinal cord interneuron specification Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter involved in ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations 2015 dataset.
ventral spinal cord interneuron fate commitment Gene Set From GO Biological Process Annotations 2015 genes participating in the ventral spinal cord interneuron fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of transcription from rna polymerase ii promoter involved in spinal cord association neuron specification Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter involved in spinal cord association neuron specification biological process from the curated GO Biological Process Annotations 2015 dataset.
ventral spinal cord interneuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the ventral spinal cord interneuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
musculoskeletal movement, spinal reflex action Gene Set From GO Biological Process Annotations 2015 genes participating in the musculoskeletal movement, spinal reflex action biological process from the curated GO Biological Process Annotations 2015 dataset.
ventral spinal cord interneuron fate determination Gene Set From GO Biological Process Annotations 2015 genes participating in the ventral spinal cord interneuron fate determination biological process from the curated GO Biological Process Annotations 2015 dataset.
cell differentiation in spinal cord Gene Set From GO Biological Process Annotations 2015 genes participating in the cell differentiation in spinal cord biological process from the curated GO Biological Process Annotations 2015 dataset.
bmp signaling pathway involved in spinal cord dorsal/ventral patterning Gene Set From GO Biological Process Annotations 2015 genes participating in the bmp signaling pathway involved in spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations 2015 dataset.
dorsal spinal cord development Gene Set From GO Biological Process Annotations 2015 genes participating in the dorsal spinal cord development biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord anterior/posterior patterning Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord anterior/posterior patterning biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord dorsal/ventral patterning Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord motor neuron migration Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord motor neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset.
corticospinal neuron axon guidance through spinal cord Gene Set From GO Biological Process Annotations 2015 genes participating in the corticospinal neuron axon guidance through spinal cord biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord development Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord development biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord motor neuron differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord motor neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
spinal cord oligodendrocyte cell fate specification Gene Set From GO Biological Process Annotations 2015 genes participating in the spinal cord oligodendrocyte cell fate specification biological process from the curated GO Biological Process Annotations 2015 dataset.
abnormality of the spinal cord Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
spinal rigidity Gene Set From GWASdb SNP-Phenotype Associations genes associated with the spinal rigidity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
widening of cervical spinal canal Gene Set From HPO Gene-Disease Associations genes associated with the widening of cervical spinal canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal dysraphism Gene Set From HPO Gene-Disease Associations genes associated with the spinal dysraphism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplastic spinal processes Gene Set From HPO Gene-Disease Associations genes associated with the hypoplastic spinal processes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
asymmetry of spinal facet joints Gene Set From HPO Gene-Disease Associations genes associated with the asymmetry of spinal facet joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the dorsal column of the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the dorsal column of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal rigidity Gene Set From HPO Gene-Disease Associations genes associated with the spinal rigidity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal canal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the spinal canal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal cord compression Gene Set From HPO Gene-Disease Associations genes associated with the spinal cord compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the spinal meninges Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the spinal meninges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal stenosis with reduced interpedicular distance Gene Set From HPO Gene-Disease Associations genes associated with the spinal stenosis with reduced interpedicular distance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pallor of dorsal columns of the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the pallor of dorsal columns of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal deformities Gene Set From HPO Gene-Disease Associations genes associated with the spinal deformities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal hemangioblastoma Gene Set From HPO Gene-Disease Associations genes associated with the spinal hemangioblastoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal instability Gene Set From HPO Gene-Disease Associations genes associated with the spinal instability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal arteriovenous malformation Gene Set From HPO Gene-Disease Associations genes associated with the spinal arteriovenous malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal cord posterior columns myelin loss Gene Set From HPO Gene-Disease Associations genes associated with the spinal cord posterior columns myelin loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal neurofibromas Gene Set From HPO Gene-Disease Associations genes associated with the spinal neurofibromas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symmetric spinal nerve root neurofibromas Gene Set From HPO Gene-Disease Associations genes associated with the symmetric spinal nerve root neurofibromas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal cord lesions Gene Set From HPO Gene-Disease Associations genes associated with the spinal cord lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy of the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the atrophy of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal cord tumor Gene Set From HPO Gene-Disease Associations genes associated with the spinal cord tumor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cervical spinal canal stenosis Gene Set From HPO Gene-Disease Associations genes associated with the cervical spinal canal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Spinal Dysraphism Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Dysraphism phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spinal Cord Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Cord Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spinal Osteophytosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Osteophytosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spinal Stenosis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Stenosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spinal Injuries Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Injuries phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spinal Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Spinal Fractures Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Spinal Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Tuberculosis, Spinal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tuberculosis, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal spinal cord dorsal column morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord dorsal column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord white matter morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord dorsal horn morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord dorsal horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord grey matter morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord grey matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal nerve morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord central canal morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord ventral horn morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord ventral horn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spinal cord size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spinal cord size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord interneuron morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord interneuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased spinal cord size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased spinal cord size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord ventral commissure morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord ventral commissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord motor column morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord motor column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord lateral column morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord lateral column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord lateral motor column morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord lateral motor column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord ependymal layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord ependymal layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spinal cord degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spinal cord degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord commissure morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord commissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal ventral spinal root morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ventral spinal root morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spinal cord ventral horn cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spinal cord ventral horn cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spinal hemorrhage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spinal hemorrhage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased spinal cord apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased spinal cord apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal cord motile cilium morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord motile cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal dorsal spinal root morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal dorsal spinal root morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal spinal reflex Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.
hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set From OMIM Gene-Disease Associations genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.
neurofibromatosis, familial spinal Gene Set From OMIM Gene-Disease Associations genes associated with the neurofibromatosis, familial spinal phenotype from the curated OMIM Gene-Disease Associations dataset.
TWIK-related spinal cord K+ channel (TRESK) Gene Set From Reactome Pathways 2014 proteins participating in the TWIK-related spinal cord K+ channel (TRESK) pathway from the Reactome Pathways dataset.
spinal column Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue spinal column from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
spinal cord Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue spinal cord from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
spinal ganglion Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue spinal ganglion from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
spinal cord Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue spinal cord in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
spinal ganglion Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue spinal ganglion in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
spinal column Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue spinal column in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
anterior spinal root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue anterior spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
spinal nerve Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue spinal nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
spinal ganglion Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue spinal ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
spinal trigeminal tract Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue spinal trigeminal tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
spinal muscle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue spinal muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
posterior spinal root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
spinal cord Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue spinal cord in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
spinal root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Spinal Cord Injury(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Spinal Cord Injury(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Spinal Cord Injury(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Spinal Cord Injury(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Spinal Meningocele Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Meningocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bulbo-Spinal Atrophy, X-Linked Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bulbo-Spinal Atrophy, X-Linked in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Canal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Canal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Compression Of Spinal Cord Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Compression Of Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Fusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Arteriovenous Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Arteriovenous Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infarction Of Spinal Cord Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infarction Of Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of The Spinal Cord Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Epidural Abscess, Spinal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Epidural Abscess, Spinal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Instability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Instability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Secondary Malignant Neoplasm Of Spinal Cord Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Secondary Malignant Neoplasm Of Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Stenosis Of Lumbar Region Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Stenosis Of Lumbar Region in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Cord Ischemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Cord Ischemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Spinal Artery Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Spinal Artery Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Cord Myelodysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Cord Myelodysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Spinal Cord Ependymoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Spinal Cord Ependymoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Cord Involvement Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Cord Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Cord Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Cord Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Hemangioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Hemangioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypomyelination With Brain Stem And Spinal Cord Involvement And Leg Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Cord Myoclonus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Cord Myoclonus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cervical Spinal Cord Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cervical Spinal Cord Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Demyelination Of Spinal Cord Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Demyelination Of Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Degenerative Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Degenerative Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Degenerative Lumbar Spinal Stenosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Degenerative Lumbar Spinal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Neurofibromas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Neurofibromas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symmetric Spinal Nerve Root Neurofibromas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symmetric Spinal Nerve Root Neurofibromas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corticostriatal-Spinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corticostriatal-Spinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Cord Hemangioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Cord Hemangioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Osteophytosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Osteophytosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
[X]Spinal Osteochondrosis, Unspecified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease [X]Spinal Osteochondrosis, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Cord Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Cord Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Rigidity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Rigidity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Dorsal Column Of The Spinal Cord Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Dorsal Column Of The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spinal Cord Posterior Columns Myelin Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Cord Posterior Columns Myelin Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Asymmetry Of Spinal Facet Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Asymmetry Of Spinal Facet Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spinal Cord Lesion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Cord Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cervical Spinal Canal Stenosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cervical Spinal Canal Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spinal Stenosis With Reduced Interpedicular Distance Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Stenosis With Reduced Interpedicular Distance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Widening Of Cervical Spinal Canal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widening Of Cervical Spinal Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Paralysis, Spinal, Quadriplegic Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paralysis, Spinal, Quadriplegic in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Spinal Cord Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Increased Spinal Bone Density Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Spinal Bone Density in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
spinal cord development Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord development biological process from the curated GO Biological Process Annotations 2023 dataset.
corticospinal neuron axon guidance through spinal cord Gene Set From GO Biological Process Annotations 2023 genes participating in the corticospinal neuron axon guidance through spinal cord biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord dorsal/ventral patterning Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations 2023 dataset.
smoothened signaling pathway involved in ventral spinal cord interneuron specification Gene Set From GO Biological Process Annotations 2023 genes participating in the smoothened signaling pathway involved in ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord ventral commissure morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord ventral commissure morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
musculoskeletal movement, spinal reflex action Gene Set From GO Biological Process Annotations 2023 genes participating in the musculoskeletal movement, spinal reflex action biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord oligodendrocyte cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord oligodendrocyte cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord association neuron differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord association neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
dorsal spinal cord interneuron posterior axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the dorsal spinal cord interneuron posterior axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
ventral spinal cord interneuron fate commitment Gene Set From GO Biological Process Annotations 2023 genes participating in the ventral spinal cord interneuron fate commitment biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord motor neuron differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord motor neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord patterning Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord patterning biological process from the curated GO Biological Process Annotations 2023 dataset.
commissural neuron differentiation in spinal cord Gene Set From GO Biological Process Annotations 2023 genes participating in the commissural neuron differentiation in spinal cord biological process from the curated GO Biological Process Annotations 2023 dataset.
ventral spinal cord interneuron differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the ventral spinal cord interneuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
BMP signaling pathway involved in spinal cord dorsal/ventral patterning Gene Set From GO Biological Process Annotations 2023 genes participating in the BMP signaling pathway involved in spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations 2023 dataset.
dorsal spinal cord interneuron anterior axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the dorsal spinal cord interneuron anterior axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
cell differentiation in spinal cord Gene Set From GO Biological Process Annotations 2023 genes participating in the cell differentiation in spinal cord biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord motor neuron cell fate specification Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2023 dataset.
ventral spinal cord interneuron specification Gene Set From GO Biological Process Annotations 2023 genes participating in the ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations 2023 dataset.
smoothened signaling pathway involved in ventral spinal cord patterning Gene Set From GO Biological Process Annotations 2023 genes participating in the smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations 2023 dataset.
dorsal spinal cord interneuron axon guidance Gene Set From GO Biological Process Annotations 2023 genes participating in the dorsal spinal cord interneuron axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal cord motor neuron migration Gene Set From GO Biological Process Annotations 2023 genes participating in the spinal cord motor neuron migration biological process from the curated GO Biological Process Annotations 2023 dataset.
spinal hemorrhage Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spinal hemorrhage phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord central canal morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord central canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal nerve morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal nerve morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal ventral spinal root morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ventral spinal root morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased spinal cord size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased spinal cord size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord interneuron morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord interneuron morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord dorsal column morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord dorsal column morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord ventral horn morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord ventral horn morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased spinal cord size Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased spinal cord size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord white matter morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord white matter morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord dorsal horn morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord dorsal horn morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spinal cord degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spinal cord degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord ependymal layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord ependymal layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord lateral column morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord lateral column morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal dorsal spinal root morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal dorsal spinal root morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spinal cord inflammation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spinal cord inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased spinal cord apoptosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased spinal cord apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord grey matter morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord grey matter morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spinal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spinal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased spinal cord ventral horn cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased spinal cord ventral horn cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord lateral motor column morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord lateral motor column morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased spinal cord weight Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased spinal cord weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord motile cilium morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord motile cilium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord ventral commissure morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord ventral commissure morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord commissure morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spinal cord commissure morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal spinal cord morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal spinal cord morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Brain - Spinal cord (cervical c-1) Gene Set From GTEx Tissue Gene Expression Profiles 2023 genes with high or low expression in Brain - Spinal cord (cervical c-1) relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.
Spinal-progenitor-like cell_Brain_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Spinal-progenitor-like cell_Brain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Spinal cord cell_Embryo_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Spinal cord cell_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Spinal cord injury Gene Set From WikiPathways Pathways 2024 proteins participating in the Spinal cord injury pathway from the WikiPathways Pathways 2024 dataset.
TWIK-related spinal cord K+ channel (TRESK) Gene Set From Reactome Pathways 2024 proteins participating in the TWIK-related spinal cord K+ channel (TRESK) pathway from the Reactome Pathways 2024 dataset.
Spinal cord_CT1_Ependymal Cell Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Ependymal Cell cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Oligodendrocyte Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Oligodendrocyte cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Oligodendrocyte Precursor Cell Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Oligodendrocyte Precursor Cell cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Astrocyte Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Astrocyte cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Microglia Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Microglia cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Endothelial Cell Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Endothelial Cell cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 1 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 1 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 2 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 2 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 3 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 3 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 4 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 4 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 5 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 5 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 6 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 6 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 7 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 7 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 8 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 8 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 9 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 9 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 10 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 10 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 11 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 11 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 12 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 12 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 1 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 1 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 2 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 2 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 3 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 3 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 4 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 4 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 5 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 5 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 6 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 6 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 7 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 7 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 8 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 8 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 9 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 9 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Ventral Excitatory Neuron 1 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Ventral Excitatory Neuron 1 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Ventral Excitatory Neuron 2 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Ventral Excitatory Neuron 2 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Ventral Excitatory Neuron 3 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Ventral Excitatory Neuron 3 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Ventral Inhibitory Neuron 1 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Ventral Inhibitory Neuron 1 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Ventral Inhibitory Neuron 2 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Ventral Inhibitory Neuron 2 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Ventral Inhibitory Neuron 3 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Ventral Inhibitory Neuron 3 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_motor neuron Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_motor neuron cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Medial Excitatory Neuron 1 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Medial Excitatory Neuron 1 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Medial Excitatory Neuron 2 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Medial Excitatory Neuron 2 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Medial Excitatory Neuron 3 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Medial Excitatory Neuron 3 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Medial Excitatory Neuron 4 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Medial Excitatory Neuron 4 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Medial Inhibitory Neuron 1 Gene Set From HuBMAP ASCT+B Annotations biomarker genes for the Spinal cord_CT1_Medial Inhibitory Neuron 1 cell type from the HuBMAP ASCT+B dataset.
Spinal cord_CT1_Astrocyte Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Astrocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 1 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 1 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 10 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 10 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 11 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 11 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 12 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 12 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 2 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 2 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 3 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 3 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 4 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 4 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 5 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 5 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 6 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 6 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 7 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 7 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 8 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 8 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Excitatory Neuron 9 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Excitatory Neuron 9 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 1 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 1 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 2 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 2 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 3 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 3 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 4 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 4 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 5 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 5 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 6 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 6 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 7 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 7 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 8 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 8 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Dorsal Inhibitory Neuron 9 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Dorsal Inhibitory Neuron 9 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Endothelial Cell Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Endothelial Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Ependymal Cell Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Ependymal Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Medial Excitatory Neuron 1 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Medial Excitatory Neuron 1 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Medial Excitatory Neuron 2 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Medial Excitatory Neuron 2 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Medial Excitatory Neuron 3 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Medial Excitatory Neuron 3 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Medial Excitatory Neuron 4 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Medial Excitatory Neuron 4 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Medial Inhibitory Neuron 1 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Medial Inhibitory Neuron 1 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Microglia Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Microglia cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Oligodendrocyte Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Oligodendrocyte cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Oligodendrocyte Precursor Cell Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Oligodendrocyte Precursor Cell cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Ventral Excitatory Neuron 1 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Ventral Excitatory Neuron 1 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Ventral Excitatory Neuron 2 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Ventral Excitatory Neuron 2 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Ventral Excitatory Neuron 3 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Ventral Excitatory Neuron 3 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Ventral Inhibitory Neuron 1 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Ventral Inhibitory Neuron 1 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Ventral Inhibitory Neuron 2 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Ventral Inhibitory Neuron 2 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_Ventral Inhibitory Neuron 3 Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_Ventral Inhibitory Neuron 3 cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
Spinal cord_CT1_motor neuron Gene Set From HuBMAP ASCT+B Augmented with RNA-seq Coexpression biomarker genes for the Spinal cord_CT1_motor neuron cell type from the HuBMAP ASCT+B Augmented with RNA-seq Coexpression dataset.
corticospinal neuron axon guidance through spinal cord Gene Set From GO Biological Process Annotations 2025 genes participating in the corticospinal neuron axon guidance through spinal cord biological process from the curated GO Biological Process Annotations 2025 dataset.
spinal cord dorsal/ventral patterning Gene Set From GO Biological Process Annotations 2025 genes participating in the spinal cord dorsal/ventral patterning biological process from the curated GO Biological Process Annotations 2025 dataset.
smoothened signaling pathway involved in ventral spinal cord interneuron specification Gene Set From GO Biological Process Annotations 2025 genes participating in the smoothened signaling pathway involved in ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations 2025 dataset.
spinal cord ventral commissure morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the spinal cord ventral commissure morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
musculoskeletal movement, spinal reflex action Gene Set From GO Biological Process Annotations 2025 genes participating in the musculoskeletal movement, spinal reflex action biological process from the curated GO Biological Process Annotations 2025 dataset.
spinal cord oligodendrocyte cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the spinal cord oligodendrocyte cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
spinal cord association neuron differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the spinal cord association neuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
dorsal spinal cord interneuron posterior axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the dorsal spinal cord interneuron posterior axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
ventral spinal cord interneuron fate commitment Gene Set From GO Biological Process Annotations 2025 genes participating in the ventral spinal cord interneuron fate commitment biological process from the curated GO Biological Process Annotations 2025 dataset.
spinal cord motor neuron differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the spinal cord motor neuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
spinal cord patterning Gene Set From GO Biological Process Annotations 2025 genes participating in the spinal cord patterning biological process from the curated GO Biological Process Annotations 2025 dataset.
commissural neuron differentiation in spinal cord Gene Set From GO Biological Process Annotations 2025 genes participating in the commissural neuron differentiation in spinal cord biological process from the curated GO Biological Process Annotations 2025 dataset.
ventral spinal cord interneuron differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the ventral spinal cord interneuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
dorsal spinal cord interneuron anterior axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the dorsal spinal cord interneuron anterior axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
cell differentiation in spinal cord Gene Set From GO Biological Process Annotations 2025 genes participating in the cell differentiation in spinal cord biological process from the curated GO Biological Process Annotations 2025 dataset.
spinal cord motor neuron cell fate specification Gene Set From GO Biological Process Annotations 2025 genes participating in the spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2025 dataset.
ventral spinal cord interneuron specification Gene Set From GO Biological Process Annotations 2025 genes participating in the ventral spinal cord interneuron specification biological process from the curated GO Biological Process Annotations 2025 dataset.
smoothened signaling pathway involved in ventral spinal cord patterning Gene Set From GO Biological Process Annotations 2025 genes participating in the smoothened signaling pathway involved in ventral spinal cord patterning biological process from the curated GO Biological Process Annotations 2025 dataset.
dorsal spinal cord interneuron axon guidance Gene Set From GO Biological Process Annotations 2025 genes participating in the dorsal spinal cord interneuron axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
spinal cord motor neuron migration Gene Set From GO Biological Process Annotations 2025 genes participating in the spinal cord motor neuron migration biological process from the curated GO Biological Process Annotations 2025 dataset.
Spinal disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Spinal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Spinal cord disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord neuroblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord neuroblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord primitive neuroectodermal neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord primitive neuroectodermal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tethered spinal cord syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tethered spinal cord syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal stenosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal stenosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal neurofibromatosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal neurofibromatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord lymphoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal chordoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal chordoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord glioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord glioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Adult spinal cord ependymoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult spinal cord ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord melanoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal ependymoma, MYCN-amplified Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal ependymoma, MYCN-amplified in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Epidural spinal canal neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Epidural spinal canal neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal canal intradural extramedullary neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal canal intradural extramedullary neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal polio Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal polio in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Anterior spinal artery syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Anterior spinal artery syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord lipoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord oligodendroglioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord oligodendroglioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal cord sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Adult spinal cord glioblastoma multiforme Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult spinal cord glioblastoma multiforme in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal cord Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Spinal cord from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal column Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Spinal column from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal ganglion Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Spinal ganglion from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal cord Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Spinal cord in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal ganglion Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Spinal ganglion in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal cord Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spinal cord in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal column Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spinal column in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal ganglion Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spinal ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal nerve Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spinal nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal muscle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spinal muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal trigeminal tract Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spinal trigeminal tract in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal muscle of thorax Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Spinal muscle of thorax in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Anterior spinal root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Anterior spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Posterior spinal root Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Spinal hemangioblastoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal hemangioblastoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neuropathic spinal arthropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuropathic spinal arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Duchenne muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Duchenne muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Merosin deficient congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Walker-Warburg congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2S Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2S phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Becker muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Becker muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Benign scapuloperoneal muscular dystrophy with cardiomyopathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Benign scapuloperoneal muscular dystrophy with cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy, type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Eichsfeld type congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Facioscapulohumeral muscular dystrophy 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Facioscapulohumeral muscular dystrophy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-dreifuss muscular dystrophy 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-dreifuss muscular dystrophy 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ullrich congenital muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-dreifuss muscular dystrophy 4, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-dreifuss muscular dystrophy 4, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epidermolysa bullosa simplex and limb girdle muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epidermolysa bullosa simplex and limb girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Emery-Dreifuss muscular dystrophy, X-linked Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Emery-Dreifuss muscular dystrophy, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Limb-girdle muscular dystrophy-dystroglycanopathy, type C2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Harmonizome 3.0

Spinal Muscular Atrophies of Childhood Gene Set

spinal muscular atrophies of childhood Gene Set

Spinal Muscular Atrophies of Childhood Gene Set

Spinal Muscular Atrophies Of Childhood Gene Set

muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set

muscular atrophy, spinal; spinal muscular atrophy Gene Set

Childhood spinal muscular atrophy Gene Set

Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene Set

Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene Set

Optic Atrophies, Hereditary Gene Set

cystic kidney diseases; kidney diseases, cystic; leber congenital amaurosis; optic atrophies, hereditary; vision disorders Gene Set

optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set

atrophies Gene Set

Olivopontocerebellar Atrophies Gene Set

Optic Atrophies, Hereditary Gene Set

Severe autosomal recessive muscular dystrophy of childhood - North African type Gene Set

Severe Autosomal Recessive Muscular Dystrophy Of Childhood - North African Type (Disorder) Gene Set

Severe Childhood Autosomal Recessive Muscular Dystrophy Gene Set

spinal canal and spinal cord meningioma Gene Set

spinal cord compression; spinal osteophytosis Gene Set

Spinal Cord Injury_CNS - Spinal Cord (MMHCC)_GSE16710 Gene Set

Spinal canal and spinal cord meningioma Gene Set

Spinal muscular atrophy, type II Gene Set

Distal spinal muscular atrophy, X-linked 3 Gene Set

Spinal muscular atrophy Gene Set

Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set

Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set

Distal spinal muscular atrophy, autosomal recessive 4 Gene Set

Spinal muscular atrophy, Jerash type Gene Set

Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set

Spinal muscular atrophy 4 Gene Set

Spinal muscular atrophy with respiratory distress 1 Gene Set

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set

Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set

Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set

SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set

Muscular Atrophy, Spinal Gene Set

spinal muscular atrophy Gene Set

adult spinal muscular atrophy Gene Set

juvenile spinal muscular atrophy Gene Set

intermediate spinal muscular atrophy Gene Set

spinal muscular atrophy Gene Set

survival motor neuron spinal muscular atrophy Gene Set

muscular atrophy, spinal Gene Set

spinal muscular atrophy Gene Set

spinal muscular atrophy phenotype Gene Set

spinal muscular atrophy Gene Set

Muscular Atrophy, Spinal Gene Set

spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set

spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set

spinal muscular atrophy with progressive myoclonic epilepsy Gene Set

spinal muscular atrophy, x-linked 2, infantile Gene Set

spinal muscular atrophy-2 Gene Set

spinal muscular atrophy-3 Gene Set

spinal muscular atrophy-1 Gene Set

spinal muscular atrophy-4 Gene Set

spinal muscular atrophy, chronic distal, autosomal recessive Gene Set

spinal muscular atrophy, jokela type Gene Set

scapuloperoneal spinal muscular atrophy Gene Set

spinal muscular atrophy, late-onset, finkel type Gene Set

{spinal muscular atrophy, type iii, modifier of} Gene Set

spinal muscular atrophy, lower extremity-predominant 1, ad Gene Set

spinal muscular atrophy, lower extremity-predominant, 2, ad Gene Set

spinal muscular atrophy, distal, x-linked 3 Gene Set

spinal and bulbar muscular atrophy of kennedy Gene Set

spinal muscular atrophy, distal, congenital nonprogressive Gene Set

Spinal Muscular Atrophy Gene Set

Acute Infantile Spinal Muscular Atrophy Gene Set

Distal Spinal Muscular Atrophy Gene Set

Proximal Spinal Muscular Atrophy Gene Set

Progressive Spinal Muscular Atrophy Gene Set

Juvenile Spinal Muscular Atrophy Gene Set

Oculopharyngeal Spinal Muscular Atrophy Gene Set

Scapuloperoneal Form Of Spinal Muscular Atrophy Gene Set

Spinal Muscular Atrophy Gene Set

Spinal muscular atrophy Gene Set

X-linked spinal muscular atrophy 2 Gene Set

Spinal muscular atrophy with lower extremity predominant Gene Set