Auditory Neuropathy Spectrum Disorder

Filters:

Results for "Auditory Neuropathy Spectrum Disorder": 9 genes, 1002 gene sets

Name
AUNX1 Gene auditory neuropathy, X-linked recessive 1
CMTX3 Gene Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant)
CMTX2 Gene Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)
HMSN5 Gene Hereditary motor and sensory neuropathy* V*
NMSR Gene Neuropathy, hereditary motor and sensory, Russe type
SPOAN Gene spastic paraplegia, optic atrophy, and neuropathy
HSN1B Gene Hereditary sensory neuropathy, type IB
HMNJ Gene Distal hereditary motor neuropathy, Jerash type
HMSNO Gene Neuropathy, hereditary motor and sensory, Okinawa type
Auditory Neuropathy Spectrum Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy Spectrum Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory neuropathy spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obsessive-compulsive disorder or autism spectrum disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obsessive-compulsive disorder or autism spectrum disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ataxia Neuropathy Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia Neuropathy Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Auditory neuropathy, autosomal recessive, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Auditory neuropathy, autosomal recessive, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auditory Neuropathy, Autosomal Dominant, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Auditory Neuropathy, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.
auditory neuropathy, autosomal dominant, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the auditory neuropathy, autosomal dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
auditory neuropathy, autosomal recessive, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the auditory neuropathy, autosomal recessive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
Auditory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Neuropathy, Autosomal Dominant, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy, Autosomal Dominant, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Neuropathy And Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory Neuropathy, Nonsyndromic Recessive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Auditory Neuropathy, Nonsyndromic Recessive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Autosomal dominant auditory neuropathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant auditory neuropathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Auditory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Auditory neuropathy-optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant auditory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant auditory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Otopalatodigital spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Otopalatodigital spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NOG-Related-Symphalangism Spectrum Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NOG-Related-Symphalangism Spectrum Disorder from the curated CTD Gene-Disease Associations dataset.
autism spectrum disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease autism spectrum disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
autism spectrum disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autism spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fetal alcohol spectrum disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fetal alcohol spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autism spectrum disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease autism spectrum disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autistic spectrum disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease autistic spectrum disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autism spectrum disorder Gene Set From GWASdb SNP-Disease Associations genes associated with the disease autism spectrum disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Zellweger Spectrum Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Zellweger Spectrum Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Otopalatodigital Spectrum Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Otopalatodigital Spectrum Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Synaptic signaling associated with autism spectrum disorder Gene Set From WikiPathways Pathways 2024 proteins participating in the Synaptic signaling associated with autism spectrum disorder pathway from the WikiPathways Pathways 2024 dataset.
Autism spectrum disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autism spectrum disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Otopalatodigital syndrome spectrum disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Otopalatodigital syndrome spectrum disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autism spectrum disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Autism spectrum disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Fetal alcohol spectrum disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fetal alcohol spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autism spectrum disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autism spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Otopalatodigital syndrome spectrum disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Otopalatodigital syndrome spectrum disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autism spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autism spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
WFS1-spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the WFS1-spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial Autism Spectrum Disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial Autism Spectrum Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autism spectrum disorder - epilepsy - arthrogryposis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autism spectrum disorder - epilepsy - arthrogryposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autism spectrum disorder due to AUTS2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autism spectrum disorder due to AUTS2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GNAO1-related developmental delay-seizures-movement disorder spectrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GNAO1-related developmental delay-seizures-movement disorder spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KIF7-related ciliopathy spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KIF7-related ciliopathy spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ITPR1-associated cerebellar ataxia spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ITPR1-associated cerebellar ataxia spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
NRXN2-related Austism Spectrum Disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the NRXN2-related Austism Spectrum Disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Holoprosencephaly spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Holoprosencephaly spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
NRXN2-related autism spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the NRXN2-related autism spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autism spectrum disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Autism spectrum disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Autism spectrum disorder or schizophrenia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Autism spectrum disorder or schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Autism spectrum disorder-related traits Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Autism spectrum disorder-related traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Restricted and repetitive behaviours in autism spectrum disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Restricted and repetitive behaviours in autism spectrum disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
schizophrenia; depressive disorder, major; bipolar disorder; delusional disorder; psychosis Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; depressive disorder, major; bipolar disorder; delusional disorder; psychosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorder; depressive disorder, major; panic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder; depressive disorder, major; panic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit disorder; conduct disorder; oppositional defiant disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit disorder; conduct disorder; oppositional defiant disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
conduct disorder; oppositional defiant disorder; antisocial personality disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease conduct disorder; oppositional defiant disorder; antisocial personality disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; attention deficit disorder; conduct disorder; oppositional defiant disorder; dementia, frontotemporal Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; attention deficit disorder; conduct disorder; oppositional defiant disorder; dementia, frontotemporal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Auditory Processing Disorder, Central Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Processing Disorder, Central in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy, Type Iic (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Motor And Sensory Neuropathy, Type Iic (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fetal Alcohol Spectrum Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Fetal Alcohol Spectrum Disorders from the curated CTD Gene-Disease Associations dataset.
gjb2 mutations--phenotypic spectrum and frequencies of gjb2 mutations Gene Set From GAD Gene-Disease Associations genes associated with the disease gjb2 mutations--phenotypic spectrum and frequencies of gjb2 mutations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cftr mutation spectrum Gene Set From GAD Gene-Disease Associations genes associated with the disease cftr mutation spectrum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spectrum Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term spectrum in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
ASD autism spectrum Gene Set From PhosphoSitePlus Phosphosite-Disease Associations proteins associated with the disease ASD autism spectrum from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
Zellweger Spectrum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Zellweger Spectrum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pik3Ca Related Overgrowth Spectrum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pik3Ca Related Overgrowth Spectrum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
WFS1-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the WFS1-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TP63-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TP63-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Zellweger spectrum disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Zellweger spectrum disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
POLG-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the POLG-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PIK3CA-Related Overgrowth Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PIK3CA-Related Overgrowth Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multicentric osteolysis nodulosis arthropathy spectrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multicentric osteolysis nodulosis arthropathy spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
FLNB-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the FLNB-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MAPT-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MAPT-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cockayne spectrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cockayne spectrum 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.
Oromandibular-limb hypogenesis spectrum Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Oromandibular-limb hypogenesis spectrum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Branchiootorenal Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Branchiootorenal Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KAT6B-Related Spectrum Disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KAT6B-Related Spectrum Disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
RECQL4-related spectrum disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the RECQL4-related spectrum disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
POLG2-related spectrum disorders Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the POLG2-related spectrum disorders phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autism spectrum disorders (social interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Autism spectrum disorders (social interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
PMC10269832-spectrum.04292-22-s0001.pdf-6-XBP1_XBP1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC10269832-spectrum.04292-22-s0001.pdf-6-XBP1_XBP1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC11237666-spectrum.03516-23-s0004.xlsx-Early_Resp_FOXJ1_high_Ciliated-Unnamed_6_FOXJ1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC11237666-spectrum.03516-23-s0004.xlsx-Early_Resp_FOXJ1_high_Ciliated-Unnamed_6_FOXJ1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC11237666-spectrum.03516-23-s0004.xlsx-FOXJ1_high_Ciliated_Cells-Unnamed_6_FOXJ1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC11237666-spectrum.03516-23-s0004.xlsx-FOXJ1_high_Ciliated_Cells-Unnamed_6_FOXJ1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-6-FOXN4_FOXN4 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-6-FOXN4_FOXN4 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-6-ZIC1_ZIC1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-6-ZIC1_ZIC1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-7-SOX5_SOX5 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-7-SOX5_SOX5 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-13-NPAS3_NPAS3 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-13-NPAS3_NPAS3 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-13-ZNF595_ZNF595 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-13-ZNF595_ZNF595 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-13-ZNF331_ZNF331 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-13-ZNF331_ZNF331 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-15-NFE2L2_NFE2L2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-15-NFE2L2_NFE2L2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-34-TAL1_TAL1 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-34-TAL1_TAL1 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-44-KLF4_KLF4 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-44-KLF4_KLF4 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-48-ZNF226_ZNF226 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-48-ZNF226_ZNF226 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-49-ZNF540_ZNF540 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-49-ZNF540_ZNF540 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-50-ZNF77_ZNF77 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-50-ZNF77_ZNF77 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-55-HOXA5_HOXA5 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-55-HOXA5_HOXA5 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-56-IRF7_IRF7 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-56-IRF7_IRF7 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-57-CIC_CIC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-57-CIC_CIC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-57-USF2_USF2 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-57-USF2_USF2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-59-ZNF101_ZNF101 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-59-ZNF101_ZNF101 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-69-NFIC_NFIC Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-69-NFIC_NFIC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-69-SNAPC4_SNAPC4 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-69-SNAPC4_SNAPC4 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-76-CENPB_CENPB Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-76-CENPB_CENPB transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-79-MAZ_MAZ Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-79-MAZ_MAZ transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-80-ZNF28_ZNF28 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-80-ZNF28_ZNF28 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
PMC12211054-spectrum.00100-25-s0002.pdf-81-ZNF678_ZNF678 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC12211054-spectrum.00100-25-s0002.pdf-81-ZNF678_ZNF678 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
bipolar disorder; affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar disorder; affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar disorder; unipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar disorder; unipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; alcoholism; attention deficit disorder; depression; neuroticism; affective disorder; suicidal behavior Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; alcoholism; attention deficit disorder; depression; neuroticism; affective disorder; suicidal behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizoaffective disorder; alcoholism; bipolar disorder; suicide Gene Set From GAD Gene-Disease Associations genes associated with the disease schizoaffective disorder; alcoholism; bipolar disorder; suicide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit hyperactivity disorder and conduct disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit hyperactivity disorder and conduct disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bipolar affective disorder; unipolar affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease bipolar affective disorder; unipolar affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
conduct disorder; hyperkinetic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease conduct disorder; hyperkinetic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
major depressive disorder and panic disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease major depressive disorder and panic disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
antisocial personality disorder attention deficit hyperactivity disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease antisocial personality disorder attention deficit hyperactivity disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; bipolar disorder; affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; bipolar disorder; affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; alcohol abuse; depressive disorder, major; dermal erythema; schizoaffective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
seasonal affective disorder; premenstrual dysphoric disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease seasonal affective disorder; premenstrual dysphoric disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit disorder; seasonal affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit disorder; seasonal affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major; bipolar disorder; affective psychoses Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; bipolar disorder; affective psychoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; schizoaffective disorder; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; schizoaffective disorder; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
depressive disorder, major; bipolar disorder; suicide Gene Set From GAD Gene-Disease Associations genes associated with the disease depressive disorder, major; bipolar disorder; suicide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; depressive disorder, major; bipolar disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; depressive disorder, major; bipolar disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol dependence, panic disorder without agoraphobia, generalized anxiety disorder, narcolepsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
anxiety disorder; depressive disorder, major; neuroticism Gene Set From GAD Gene-Disease Associations genes associated with the disease anxiety disorder; depressive disorder, major; neuroticism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; schizoaffective disorder; affective disorder Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; schizoaffective disorder; affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
attention deficit disorder; conduct disorder; aggressive behavior Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit disorder; conduct disorder; aggressive behavior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Schizophrenia, schizoaffective disorder or bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Schizophrenia, schizoaffective disorder or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Attention deficit hyperactivity disorder and conduct disorder Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Attention deficit hyperactivity disorder and conduct disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder and major depressive disorder (combined) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Bipolar disorder and major depressive disorder (combined) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Bipolar disorder (age of onset <21) or attention deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder (age of onset <21) or attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bipolar disorder or attention deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder or attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Oppositional defiant disorder dimensions in attention-deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Oppositional defiant disorder dimensions in attention-deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Eating disorder in bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Eating disorder in bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bipolar disorder and eating disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder and eating disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HIV-associated neurocognitive disorder (mild neurocognitive disorder or asymptomatic neurocognitive impairment) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIV-associated neurocognitive disorder (mild neurocognitive disorder or asymptomatic neurocognitive impairment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HIV-associated neurocognitive disorder (mild neurocognitive disorder) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIV-associated neurocognitive disorder (mild neurocognitive disorder) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Functional impairment in major depressive disorder, bipolar disorder and schizophrenia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Functional impairment in major depressive disorder, bipolar disorder and schizophrenia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, schizoaffective disorder or bipolar disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, schizoaffective disorder or bipolar disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disruptive behavior disorder and attention deficit hyperactivity disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disruptive behavior disorder and attention deficit hyperactivity disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Attention deficit hyperactivity disorder and conduct disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Attention deficit hyperactivity disorder and conduct disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bipolar disorder or major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bipolar disorder or major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or major depressive disorder x sex interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or major depressive disorder x sex interaction (3df) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or major depressive disorder x sex interaction (3df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Schizophrenia, bipolar disorder or recurrent major depressive disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Schizophrenia, bipolar disorder or recurrent major depressive disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
primary auditory cortex (core)_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_21 pcw_F_12365 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_25 pcw_F_12948 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_25 pcw_F_12948 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_13 pcw_M_12820 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
primary auditory cortex (core)_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_11 yrs_F_12289 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_25 pcw_F_12948 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_25 pcw_F_12948 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_37 pcw_M_263195015 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_4 mos_M_12889 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_4 mos_M_12889 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_8 yrs_M_12981 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_13 pcw_M_12820 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_4 mos_M_12890 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
primary auditory cortex (core)_19 yrs_F_12832 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
MZ in primary auditory cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SG in primary auditory cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer CP in primary auditory cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner CP in primary auditory cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in primary auditory cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
IZ in primary auditory cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Auditory Perceptual Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Auditory Perceptual Disorders from the curated CTD Gene-Disease Associations dataset.
auditory system disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease auditory system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
auditory system disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease auditory system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
auditory system disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease auditory system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
auditory agnosia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease auditory agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
auditory system cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease auditory system cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
verbal auditory agnosia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease verbal auditory agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
auditory evoked potential Gene Set From GAD Gene-Disease Associations genes associated with the disease auditory evoked potential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
auditory Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term auditory in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
auditory receptor cell fate specification Gene Set From GO Biological Process Annotations 2015 genes participating in the auditory receptor cell fate specification biological process from the curated GO Biological Process Annotations 2015 dataset.
auditory receptor cell stereocilium organization Gene Set From GO Biological Process Annotations 2015 genes participating in the auditory receptor cell stereocilium organization biological process from the curated GO Biological Process Annotations 2015 dataset.
auditory receptor cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
auditory receptor cell morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the auditory receptor cell morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of auditory receptor cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
auditory receptor cell fate commitment Gene Set From GO Biological Process Annotations 2015 genes participating in the auditory receptor cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset.
auditory behavior Gene Set From GO Biological Process Annotations 2015 genes participating in the auditory behavior biological process from the curated GO Biological Process Annotations 2015 dataset.
auditory receptor cell development Gene Set From GO Biological Process Annotations 2015 genes participating in the auditory receptor cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of auditory receptor cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of auditory receptor cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
response to auditory stimulus Gene Set From GO Biological Process Annotations 2015 genes participating in the response to auditory stimulus biological process from the curated GO Biological Process Annotations 2015 dataset.
auditory receptor cell fate determination Gene Set From GO Biological Process Annotations 2015 genes participating in the auditory receptor cell fate determination biological process from the curated GO Biological Process Annotations 2015 dataset.
auditory system disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease auditory system disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
auditory hallucinations Gene Set From HPO Gene-Disease Associations genes associated with the auditory hallucinations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dilatated internal auditory canal Gene Set From HPO Gene-Disease Associations genes associated with the dilatated internal auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the internal auditory canal Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the internal auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent brainstem auditory responses Gene Set From HPO Gene-Disease Associations genes associated with the absent brainstem auditory responses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal auditory evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the abnormal auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atresia of the external auditory canal Gene Set From HPO Gene-Disease Associations genes associated with the atresia of the external auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
auditory auras Gene Set From HPO Gene-Disease Associations genes associated with the auditory auras phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
prolonged brainstem auditory evoked potentials Gene Set From HPO Gene-Disease Associations genes associated with the prolonged brainstem auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the auditory canal Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
exostosis of the external auditory canal Gene Set From HPO Gene-Disease Associations genes associated with the exostosis of the external auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slit-like opening of the exterior auditory meatus Gene Set From HPO Gene-Disease Associations genes associated with the slit-like opening of the exterior auditory meatus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
stenosis of the external auditory canal Gene Set From HPO Gene-Disease Associations genes associated with the stenosis of the external auditory canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Auditory Perceptual Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Auditory Perceptual Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Auditory Perception Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Auditory Perception phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Auditory Threshold Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Auditory Threshold phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal auditory brainstem response waveform shape Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response waveform shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal auditory brainstem response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal auditory summating potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory summating potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal auditory tube Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory tube phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased threshold for auditory brainstem response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased threshold for auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal external auditory canal morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal external auditory canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased or absent threshold for auditory brainstem response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased or absent threshold for auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal auditory cortex tonotopy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory cortex tonotopy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent external auditory canal Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent external auditory canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal internal auditory canal morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal internal auditory canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent auditory tube Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent auditory tube phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal auditory cortex morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
auditory cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue auditory cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
auditory vesicle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue auditory vesicle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
External Auditory Canal, Bilateral Atresia Of, With Congenital Vertical Talus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease External Auditory Canal, Bilateral Atresia Of, With Congenital Vertical Talus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Auditory And Visual Hallucinations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory And Visual Hallucinations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Absence, Atresia And Stricture Of Auditory Canal (External) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Absence, Atresia And Stricture Of Auditory Canal (External) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Seizures, Auditory Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Seizures, Auditory in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Narrow Internal Auditory Canal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Narrow Internal Auditory Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Auditory Inattention Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Auditory Inattention in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dilatated Internal Auditory Canal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dilatated Internal Auditory Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Auditory Evoked Potential Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Auditory Evoked Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Verbal Auditory Hallucinations Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Verbal Auditory Hallucinations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Focal Sensory Auditory Seizure Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Focal Sensory Auditory Seizure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Brainstem Auditory Responses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Brainstem Auditory Responses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Prolonged Brainstem Auditory Evoked Potentials Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prolonged Brainstem Auditory Evoked Potentials in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Auditory Canal Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Auditory Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
auditory receptor cell stereocilium organization Gene Set From GO Biological Process Annotations 2023 genes participating in the auditory receptor cell stereocilium organization biological process from the curated GO Biological Process Annotations 2023 dataset.
response to auditory stimulus Gene Set From GO Biological Process Annotations 2023 genes participating in the response to auditory stimulus biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of inner ear auditory receptor cell fate specification Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of inner ear auditory receptor cell fate specification biological process from the curated GO Biological Process Annotations 2023 dataset.
auditory behavior Gene Set From GO Biological Process Annotations 2023 genes participating in the auditory behavior biological process from the curated GO Biological Process Annotations 2023 dataset.
auditory receptor cell development Gene Set From GO Biological Process Annotations 2023 genes participating in the auditory receptor cell development biological process from the curated GO Biological Process Annotations 2023 dataset.
auditory receptor cell fate commitment Gene Set From GO Biological Process Annotations 2023 genes participating in the auditory receptor cell fate commitment biological process from the curated GO Biological Process Annotations 2023 dataset.
inner ear auditory receptor cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the inner ear auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
auditory receptor cell morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the auditory receptor cell morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of inner ear auditory receptor cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of inner ear auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
absent external auditory canal Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent external auditory canal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal external auditory canal morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal external auditory canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased or absent threshold for auditory brainstem response Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased or absent threshold for auditory brainstem response phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal auditory brainstem response Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal auditory brainstem response phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal auditory brainstem response waveform shape Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal auditory brainstem response waveform shape phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent auditory tube Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent auditory tube phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent auditory bulla Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent auditory bulla phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal internal auditory canal morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal internal auditory canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal auditory tube morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal auditory tube morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal auditory bulla morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal auditory bulla morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal auditory cortex morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal auditory cortex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal auditory summating potential Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal auditory summating potential phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased threshold for auditory brainstem response Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased threshold for auditory brainstem response phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
external auditory canal stenosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the external auditory canal stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal auditory cortex tonotopy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal auditory cortex tonotopy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal auditory brainstem response Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal auditory brainstem response phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
auditory receptor cell stereocilium organization Gene Set From GO Biological Process Annotations 2025 genes participating in the auditory receptor cell stereocilium organization biological process from the curated GO Biological Process Annotations 2025 dataset.
response to auditory stimulus Gene Set From GO Biological Process Annotations 2025 genes participating in the response to auditory stimulus biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of inner ear auditory receptor cell fate specification Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of inner ear auditory receptor cell fate specification biological process from the curated GO Biological Process Annotations 2025 dataset.
auditory behavior Gene Set From GO Biological Process Annotations 2025 genes participating in the auditory behavior biological process from the curated GO Biological Process Annotations 2025 dataset.
auditory receptor cell development Gene Set From GO Biological Process Annotations 2025 genes participating in the auditory receptor cell development biological process from the curated GO Biological Process Annotations 2025 dataset.
auditory receptor cell fate commitment Gene Set From GO Biological Process Annotations 2025 genes participating in the auditory receptor cell fate commitment biological process from the curated GO Biological Process Annotations 2025 dataset.
inner ear auditory receptor cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the inner ear auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
auditory receptor cell morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the auditory receptor cell morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of inner ear auditory receptor cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of inner ear auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
Auditory system disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Auditory system disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Auditory system disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Auditory system disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Auditory system disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Auditory system disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Auditory agnosia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Auditory agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Verbal auditory agnosia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Verbal auditory agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Auditory system benign neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Auditory system benign neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Auditory system cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Auditory system cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Internal auditory canal meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Internal auditory canal meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Internal auditory canal lipoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Internal auditory canal lipoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Auditory cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Auditory cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Auditory vesicle Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Auditory vesicle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Auditory capsule Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Auditory capsule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neuromuscular disease and ocular or auditory anomalies Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuromuscular disease and ocular or auditory anomalies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Trifunctional protein deficiency with myopathy and neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Trifunctional protein deficiency with myopathy and neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Giant axonal neuropathy, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Giant axonal neuropathy, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy hereditary sensory and autonomic type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, hereditary motor and sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE IE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE ID Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE ID phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE IF Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinocerebellar ataxia autosomal recessive with axonal neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia autosomal recessive with axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary motor and sensory neuropathy with optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
46,XY gonadal dysgenesis, partial, with minifascicular neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY, TYPE IC Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked hereditary motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set From ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary sensory and autonomic neuropathy type IIA Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Giant axonal neuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Giant axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.
Hereditary Sensory and Motor Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type IIB from the curated CTD Gene-Disease Associations dataset.
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, Russe type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Russe type from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Distal Hereditary Motor, Type IIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type IIA from the curated CTD Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.
Sciatic Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sciatic Neuropathy from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy, Type IIC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset.
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy from the curated CTD Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy VI Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Motor And Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, Okinawa type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.
LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset.
Tomaculous neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tomaculous neuropathy from the curated CTD Gene-Disease Associations dataset.
Sensorimotor neuropathy with ataxia, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensorimotor neuropathy with ataxia, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset.
46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy from the curated CTD Gene-Disease Associations dataset.
Giant Axonal Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Giant Axonal Neuropathy from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Distal Hereditary Motor, Type VIIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.
Optic Neuropathy, Ischemic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Neuropathy, Ischemic from the curated CTD Gene-Disease Associations dataset.
Neuropathy, hereditary motor and sensory, LOM type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, hereditary motor and sensory, LOM type from the curated CTD Gene-Disease Associations dataset.
Inherited Peripheral Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Inherited Peripheral Neuropathy from the curated CTD Gene-Disease Associations dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis from the curated CTD Gene-Disease Associations dataset.
peripheral neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease peripheral neuropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
brachial plexus neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease brachial plexus neuropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
hereditary sensory neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary sensory neuropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease neuropathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
brachial plexus neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease brachial plexus neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary sensory neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary sensory neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
inflammatory and toxic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inflammatory and toxic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autonomic peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autonomic peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sciatic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sciatic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alcoholic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcoholic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tibial neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tibial neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
toxic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease toxic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sensory peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sensory peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
asymmetric motor neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease asymmetric motor neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diabetic autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diabetic autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
uremic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease uremic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
femoral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease femoral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
leber hereditary optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease leber hereditary optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
distal hereditary motor neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal hereditary motor neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
axonal neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease axonal neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
peroneal neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peroneal neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
median neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease median neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
radial neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease radial neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
motor peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease motor peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ischemic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ischemic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
diabetic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease diabetic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
ulnar neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ulnar neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neuropathy, hereditary motor and sensory Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy, hereditary motor and sensory in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy type 1b Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth neuropathy type 1b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetic neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hyperlipidemias; hypertension; optic neuropathy, ischemic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
leber's hereditary optic neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease leber's hereditary optic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuropathy, charcot-marie-tooth Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy, charcot-marie-tooth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholic neuropathy; alcoholism; folic acid deficiency; hyperhomocysteinemia; liver diseases, alcoholic Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholic neuropathy; alcoholism; folic acid deficiency; hyperhomocysteinemia; liver diseases, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nephropathy, diabetic; retinopathy, diabetic; neuropathy, diabetic; microalbuminuria, diabetic Gene Set From GAD Gene-Disease Associations genes associated with the disease nephropathy, diabetic; retinopathy, diabetic; neuropathy, diabetic; microalbuminuria, diabetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuropathy, alzheimer's disease related Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy, alzheimer's disease related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuropathy, diabetic Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy, diabetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcohol-related polyneuropathy; alcoholic neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease alcohol-related polyneuropathy; alcoholic neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
charcot-marie-tooth disease; hereditary sensory and motor neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuropathy, small fiber Gene Set From GAD Gene-Disease Associations genes associated with the disease neuropathy, small fiber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperhomocysteinemia; optic neuropathy, ischemic Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; optic neuropathy, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dejerine-sottas neuropathy Gene Set From GAD Gene-Disease Associations genes associated with the disease dejerine-sottas neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neuropathy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term neuropathy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Paclitaxel-induced neuropathy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Paclitaxel-induced neuropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
peripheral neuropathy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease peripheral neuropathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
sensory peripheral neuropathy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease sensory peripheral neuropathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
neuropathy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease neuropathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
peripheral neuropathy Gene Set From GWASdb SNP-Phenotype Associations genes associated with the peripheral neuropathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sensory neuropathy Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sensory neuropathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sensory axonal neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the sensory axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
chronic axonal neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the chronic axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral axonal neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the peripheral axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the optic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
demyelinating motor neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the demyelinating motor neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor axonal neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the motor axonal neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
demyelinating peripheral neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the demyelinating peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sensory ataxic neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the sensory ataxic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive peripheral neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene Set From HPO Gene-Disease Associations genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
entrapment neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the entrapment neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sensorimotor neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the sensorimotor neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
constrictive median neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the constrictive median neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
episodic peripheral neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the episodic peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonarteritic anterior ischemic optic neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the nonarteritic anterior ischemic optic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sensory neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the sensory neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal peripheral sensory neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the distal peripheral sensory neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Hereditary Sensory and Motor Neuropathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hereditary Sensory and Motor Neuropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Alcoholic Neuropathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Alcoholic Neuropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Median Neuropathy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Median Neuropathy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Neuropathy, Ischemic Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Neuropathy, Ischemic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
optic neuropathy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic neuropathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
?neuropathy, hereditary sensory and autonomic, type vi Gene Set From OMIM Gene-Disease Associations genes associated with the ?neuropathy, hereditary sensory and autonomic, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, with spastic paraplegia Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, with spastic paraplegia phenotype from the curated OMIM Gene-Disease Associations dataset.
neuromyotonia and axonal neuropathy, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the neuromyotonia and axonal neuropathy, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type ic Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type ic phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type ii Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, congenital hypomyelinating, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, congenital hypomyelinating, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type iic Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type iib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.
giant axonal neuropathy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the giant axonal neuropathy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, paraneoplastic sensory Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, paraneoplastic sensory phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, motor and sensory, russe type Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, motor and sensory, russe type phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, jerash type Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, jerash type phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy v Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy v phenotype from the curated OMIM Gene-Disease Associations dataset.
?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
46xy partial gonadal dysgenesis, with minifascicular neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the 46xy partial gonadal dysgenesis, with minifascicular neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type ie Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type ie phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type id Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type id phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type if Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type if phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
congenital cataracts, facial dysmorphism, and neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the congenital cataracts, facial dysmorphism, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
agenesis of the corpus callosum with peripheral neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the agenesis of the corpus callosum with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked recessive, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked recessive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked recessive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia, optic atrophy, and neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
{nonarteritic anterior ischemic optic neuropathy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {nonarteritic anterior ischemic optic neuropathy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
small fiber neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the small fiber neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
charcot-marie-tooth neuropathy, x-linked dominant, 1 Gene Set From OMIM Gene-Disease Associations genes associated with the charcot-marie-tooth neuropathy, x-linked dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary motor and sensory, russe type Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary motor and sensory, russe type phenotype from the curated OMIM Gene-Disease Associations dataset.
deafness, autosomal dominant, with peripheral neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant, with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy, proximal type Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy, proximal type phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type va Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy, type iic Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, recurrent, with pressure palsies Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, recurrent, with pressure palsies phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, inflammatory demyelinating Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, inflammatory demyelinating phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type vii Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type vii phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy vi Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy vi phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type viib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset.
?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set From OMIM Gene-Disease Associations genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, hereditary sensory and autonomic, type v Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type v phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy with dystonia and motor neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy with dystonia and motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, congenital hypomyelinating Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, congenital hypomyelinating phenotype from the curated OMIM Gene-Disease Associations dataset.
spinocerebellar ataxia, autosomal recessive with axonal neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spinocerebellar ataxia, autosomal recessive with axonal neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
?giant axonal neuropathy 2, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the ?giant axonal neuropathy 2, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type iib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type iia Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset.
Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Motor And Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Motor And Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tangier Disease Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tangier Disease Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Small Fiber Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Small Fiber Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Neuropathy Due To And Following Chemotherapy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Neuropathy Due To And Following Chemotherapy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sciatic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sciatic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Demyelinating Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensorimotor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensorimotor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Trifunctional Protein Deficiency With Myopathy And Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arteritic Anterior Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arteritic Anterior Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autonomic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonarteritic Anterior Ischemic Optic Neuropathy (Naion) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonarteritic Anterior Ischemic Optic Neuropathy (Naion) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Sensory Autonomic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sensory Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hmn (Hereditary Motor Neuropathy) Proximal Type I Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hmn (Hereditary Motor Neuropathy) Proximal Type I in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visceral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visceral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Alcoholic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Alcoholic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vasculitic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vasculitic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Axonal Sensorimotor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Axonal Sensorimotor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor And Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Motor And Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensory And Autonomic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensory And Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cardiac Autonomic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cardiac Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Amyloid Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Amyloid Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Amyloid Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Amyloid Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Unspecified Idiopathic Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Unspecified Idiopathic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Constrictive Median Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Constrictive Median Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensory Neuropathy, Hereditary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensory Neuropathy, Hereditary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periodic Paralysis With Later-Onset Distal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodic Paralysis With Later-Onset Distal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anti-Mag Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anti-Mag Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Giant Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Giant Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Optic Neuropathy, Ischemic Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Neuropathy, Ischemic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asymmetric Diabetic Proximal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asymmetric Diabetic Proximal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symmetric Diabetic Proximal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symmetric Diabetic Proximal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multifocal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multifocal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inflammatory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Hypomyelinating Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Hypomyelinating Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypertrophic Neuropathy Of Infancy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypertrophic Neuropathy Of Infancy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Motor Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Motor Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Length-Dependent Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Length-Dependent Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Giant Axonal Neuropathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Giant Axonal Neuropathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Hereditary Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Hereditary Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Peripheral Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Peripheral Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inherited Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inherited Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Sensory And Autonomic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sensory And Autonomic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Sensory Radicular Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Sensory Radicular Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dejerine-Sottas Neuropathy, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dejerine-Sottas Neuropathy, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Arteritic Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Arteritic Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult Polyglucosan Body Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult Polyglucosan Body Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Anterior Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Anterior Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Ischemic Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hiv Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hiv Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Motor Sensory Axonal Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Motor Sensory Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hereditary And Idiopathic Neuropathy, Unspecified Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hereditary And Idiopathic Neuropathy, Unspecified in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Early-Onset Axonal Neuropathy Due To Mitofusin 2 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inherited Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inherited Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Median Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Median Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Demyelinating Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Demyelinating Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dominantly Inherited Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominantly Inherited Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hollow Visceral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hollow Visceral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ischemic Peripheral Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor Axonal Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Motor Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Peripheral Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sensory Axonal Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sensory Axonal Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sensory Ataxic Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sensory Ataxic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Episodic Peripheral Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Neuropathy With Sensorineural Hearing Impairment Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Neuropathy With Sensorineural Hearing Impairment Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Demyelinating Motor Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Demyelinating Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
optic neuropathy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic neuropathy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Intracellular trafficking proteins involved in CMT neuropathy Gene Set From WikiPathways Pathways 2024 proteins participating in the Intracellular trafficking proteins involved in CMT neuropathy pathway from the WikiPathways Pathways 2024 dataset.
Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN) pathway from the Reactome Pathways 2024 dataset.
Neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Leber hereditary optic neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Leber hereditary optic neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinocerebellar ataxia with axonal neuropathy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Brachial plexus neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Brachial plexus neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Agenesis of the corpus callosum with peripheral neuropathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Agenesis of the corpus callosum with peripheral neuropathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary neuropathy with liability to pressure palsies Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary neuropathy with liability to pressure palsies from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 1E Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory neuropathy type 1E from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hereditary sensory and autonomic neuropathy type 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Neuropathy Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Neuropathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leber hereditary optic neuropathy and dystonia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leber hereditary optic neuropathy and dystonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diabetic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diabetic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leber hereditary optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Leber hereditary optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Axonal neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Axonal neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Tibial neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Tibial neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Brachial plexus neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Brachial plexus neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary neuropathy with liability to pressure palsies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary neuropathy with liability to pressure palsies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-arteritic anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-arteritic anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Motor peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Motor peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Toxic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Toxic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sensory peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sensory peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Inflammatory and toxic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inflammatory and toxic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Arteritic anterior ischemic optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Arteritic anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinocerebellar ataxia with axonal neuropathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinocerebellar ataxia with axonal neuropathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sciatic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sciatic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 2C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 2C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nutritional optic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nutritional optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Diabetic autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diabetic autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 1E Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1E in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Uremic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Uremic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autonomic peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autonomic peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Alcoholic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alcoholic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peroneal neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peroneal neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Agenesis of the corpus callosum with peripheral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Agenesis of the corpus callosum with peripheral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 1C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 1C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ulnar neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ulnar neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Ischemic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ischemic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Radial neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Radial neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 1D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory and autonomic neuropathy type 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory and autonomic neuropathy type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 1F Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 1F in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Femoral neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Femoral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Median neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Median neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic peripheral autonomic neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic peripheral autonomic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Giant axonal neuropathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Giant axonal neuropathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Giant axonal neuropathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Giant axonal neuropathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Asymmetric motor neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Asymmetric motor neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary sensory neuropathy type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary sensory neuropathy type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary sensory and autonomic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary sensory and autonomic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral axonal neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Adult polyglucosan body neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult polyglucosan body neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nonarteritic anterior ischemic optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonarteritic anterior ischemic optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sensorimotor neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sensorimotor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Giant axonal neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Giant axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataracts-facial dysmorphism-neuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataracts-facial dysmorphism-neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth Neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Sensory ataxic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sensory ataxic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal hereditary motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal hereditary motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dejerine-sottas neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dejerine-sottas neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary sensory neuropathy-deafness-dementia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary sensory neuropathy-deafness-dementia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Demyelinating peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Demyelinating peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive axonal neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Familial dilated cardiomyopathy and peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Familial dilated cardiomyopathy and peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Small fiber neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Small fiber neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive demyelinating neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive demyelinating neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visceral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visceral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant hereditary axonal motor and sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant hereditary axonal motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary sensorimotor neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary sensorimotor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GARS-Associated Axonal Neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GARS-Associated Axonal Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital sensory neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leber-like hereditary optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leber-like hereditary optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leber hereditary optic neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leber hereditary optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Peripheral motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital hypomyelination neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital hypomyelination neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diabetic neuropathy in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic neuropathy in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Sensory peripheral neuropathy in microtubule targeting agent-treated breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sensory peripheral neuropathy in microtubule targeting agent-treated breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neuropathy x type 2 diabetes interaction Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neuropathy x type 2 diabetes interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bortezomib-induced peripheral neuropathy in multiple myeloma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bortezomib-induced peripheral neuropathy in multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Diabetic peripheral neuropathy in type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diabetic peripheral neuropathy in type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Paclitaxel-induced neuropathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Paclitaxel-induced neuropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Vincristine-induced peripheral neuropathy in acute lymphoblastic leukemia Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Vincristine-induced peripheral neuropathy in acute lymphoblastic leukemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Docetaxel-induced peripheral neuropathy in metastatic castrate-resistant prostate cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Docetaxel-induced peripheral neuropathy in metastatic castrate-resistant prostate cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Taxane-induced peripheral neuropathy in breast cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Taxane-induced peripheral neuropathy in breast cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Foot ulcer in diabetes and neuropathy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Foot ulcer in diabetes and neuropathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Peroxisome biogenesis disorder 9B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 9B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 3A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 3A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-telangiectasia-like disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 8B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 8B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 8A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 8A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisomal fatty acyl-coa reductase 1 disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisomal fatty acyl-coa reductase 1 disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 7B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 7A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 7A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rett's disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rett's disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Nijmegen breakage syndrome-like disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Nijmegen breakage syndrome-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Platelet-type bleeding disorder 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Platelet-type bleeding disorder 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Platelet-type bleeding disorder 15 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Platelet-type bleeding disorder 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Platelet-type bleeding disorder 17 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Platelet-type bleeding disorder 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Platelet-type bleeding disorder 16 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Platelet-type bleeding disorder 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1s Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2L Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set From ClinVar Gene-Phenotype Associations genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 2k Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1Q Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1P Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1N Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1v Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Ataxia-telangiectasia-like disorder 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Ataxia-telangiectasia-like disorder 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Familial platelet disorder with associated myeloid malignancy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Familial platelet disorder with associated myeloid malignancy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Focal epilepsy with speech disorder with or without mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type Ix Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 4B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 5A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 5A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 5B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1I Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1K Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1O Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1E Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1y Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1u Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Congenital disorder of glycosylation type 1t Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital disorder of glycosylation type 1t phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 11A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 11A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 11B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 11B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bleeding disorder, platelet-type, 19 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bleeding disorder, platelet-type, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Bleeding disorder, platelet-type, 18 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bleeding disorder, platelet-type, 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 13A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 13A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Speech-language disorder 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Speech-language disorder 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 6A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 6A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Peroxisome biogenesis disorder 6B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Peroxisome biogenesis disorder 6B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aortic valve disorder Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aortic valve disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Stereotypic Movement Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Stereotypic Movement Disorder from the curated CTD Gene-Disease Associations dataset.
Tobacco Use Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Tobacco Use Disorder from the curated CTD Gene-Disease Associations dataset.
Speech-Sound Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Speech-Sound Disorder from the curated CTD Gene-Disease Associations dataset.
Platelet Disorder, Familial, with Associated Myeloid Malignancy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Platelet Disorder, Familial, with Associated Myeloid Malignancy from the curated CTD Gene-Disease Associations dataset.
Orthostatic Hypotensive Disorder, Streeten Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Orthostatic Hypotensive Disorder, Streeten Type from the curated CTD Gene-Disease Associations dataset.
Paroxysmal Extreme Pain Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Paroxysmal Extreme Pain Disorder from the curated CTD Gene-Disease Associations dataset.
NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH OR WITHOUT JUVENILE MYELOMONOCYTIC LEUKEMIA from the curated CTD Gene-Disease Associations dataset.
Autistic Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Autistic Disorder from the curated CTD Gene-Disease Associations dataset.
Transient Myeloproliferative Disorder of Down Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Transient Myeloproliferative Disorder of Down Syndrome from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIF Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIF from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1A from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation, type 2C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation, type 2C from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2D from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.
Conduct Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Conduct Disorder from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1G from the curated CTD Gene-Disease Associations dataset.
Pigmentary Disorder, Reticulate, with Systemic Manifestations Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pigmentary Disorder, Reticulate, with Systemic Manifestations from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder of Glycosylation, Type Io Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.
Bleeding Disorder, East Texas Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bleeding Disorder, East Texas Type from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type Im Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type Im from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type In Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type In from the curated CTD Gene-Disease Associations dataset.
Bipolar Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bipolar Disorder from the curated CTD Gene-Disease Associations dataset.
ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.
PEROXISOME BIOGENESIS DISORDER 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PEROXISOME BIOGENESIS DISORDER 2B from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1H Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1H from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 8 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 9 from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1J Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1J from the curated CTD Gene-Disease Associations dataset.
Obsessive-Compulsive Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Obsessive-Compulsive Disorder from the curated CTD Gene-Disease Associations dataset.
Nijmegen Breakage Syndrome-Like Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nijmegen Breakage Syndrome-Like Disorder from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1B from the curated CTD Gene-Disease Associations dataset.
REM Sleep Behavior Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease REM Sleep Behavior Disorder from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2A from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 2E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 2E from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip from the curated CTD Gene-Disease Associations dataset.
Depressive Disorder, Major Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Depressive Disorder, Major from the curated CTD Gene-Disease Associations dataset.
Antisocial Personality Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Antisocial Personality Disorder from the curated CTD Gene-Disease Associations dataset.
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset.
Myeloproliferative Disorder, Chronic, with Eosinophilia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myeloproliferative Disorder, Chronic, with Eosinophilia from the curated CTD Gene-Disease Associations dataset.
BLEEDING DISORDER, PLATELET-TYPE, 8 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease BLEEDING DISORDER, PLATELET-TYPE, 8 from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1F Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1F from the curated CTD Gene-Disease Associations dataset.
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj from the curated CTD Gene-Disease Associations dataset.
Major Depressive Disorder 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Depressive Disorder 1 from the curated CTD Gene-Disease Associations dataset.
Major Depressive Disorder 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Depressive Disorder 2 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 4 from the curated CTD Gene-Disease Associations dataset.
Attention Deficit Disorder with Hyperactivity Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Attention Deficit Disorder with Hyperactivity from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type II Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type II from the curated CTD Gene-Disease Associations dataset.
NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1K Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1K from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1L Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1L from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1C Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1C from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1E Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1E from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation type 1D Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation type 1D from the curated CTD Gene-Disease Associations dataset.
Congenital disorder of glycosylation, type 2G Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital disorder of glycosylation, type 2G from the curated CTD Gene-Disease Associations dataset.
Depressive Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Depressive Disorder from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIH Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIH from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 2 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 3 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 1 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 6 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 7 from the curated CTD Gene-Disease Associations dataset.
Major Affective Disorder 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Major Affective Disorder 5 from the curated CTD Gene-Disease Associations dataset.
Panic Disorder Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Panic Disorder from the curated CTD Gene-Disease Associations dataset.
SPEECH-LANGUAGE DISORDER 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SPEECH-LANGUAGE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.
Congenital Disorder Of Glycosylation, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIB from the curated CTD Gene-Disease Associations dataset.
Tobacco Use Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Tobacco Use Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Depressive Disorder, Major Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Depressive Disorder, Major in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Depressive Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Depressive Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Autistic Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Autistic Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Conduct Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Conduct Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Panic Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Panic Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Bipolar Disorder Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Bipolar Disorder in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
Attention Deficit Disorder with Hyperactivity Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Attention Deficit Disorder with Hyperactivity in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
congenital disorder of glycosylation Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital disorder of glycosylation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
carbohydrate metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease carbohydrate metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cognitive disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cognitive disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
metal metabolism disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease metal metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
glycogen metabolism disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease glycogen metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
urea cycle disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease urea cycle disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
pervasive developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease pervasive developmental disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
physical disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease physical disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease specific developmental disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
gamma-amino butyric acid metabolism disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease gamma-amino butyric acid metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
tic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease tic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
purine-pyrimidine metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease purine-pyrimidine metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
sleep disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease sleep disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
bilirubin metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease bilirubin metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
amino acid metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease amino acid metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
inherited metabolic disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease inherited metabolic disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease developmental disorder of mental health from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
lipid metabolism disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease lipid metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
psychotic disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease psychotic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
sexual disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease sexual disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
cognitive disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease cognitive disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
mood disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease mood disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
conduct disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease conduct disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
substance-related disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease substance-related disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
physical disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease physical disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
impulse control disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease impulse control disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease specific developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
attention deficit hyperactivity disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease attention deficit hyperactivity disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
inherited metabolic disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease inherited metabolic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
bipolar disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease bipolar disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
panic disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease panic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
eating disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease eating disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
tic disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease tic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
sleep disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease sleep disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
autistic disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease autistic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease developmental disorder of mental health in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
lipid metabolism disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease lipid metabolism disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
pervasive developmental disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease pervasive developmental disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
personality disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease personality disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
anxiety disorder Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease anxiety disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
stereotypic movement disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease stereotypic movement disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bipolar disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bipolar disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
body dysmorphic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease body dysmorphic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation type ii Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation type ii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
somatization disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease somatization disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cyclothymic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cyclothymic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
paraphilia disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease paraphilia disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
tic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease tic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
lipid metabolism disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lipid metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
panic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease panic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
histrionic personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease histrionic personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
psychotic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease psychotic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schizotypal personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease schizotypal personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sexual disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sexual disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
carbohydrate metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease carbohydrate metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
vitamin metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vitamin metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mood disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mood disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
neurotic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neurotic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
conduct disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease conduct disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
post-traumatic stress disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease post-traumatic stress disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic tic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic tic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
urea cycle disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urea cycle disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
avoidant personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease avoidant personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pervasive developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pervasive developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
glycogen metabolism disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease glycogen metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dysthymic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dysthymic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
periodic limb movement disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease periodic limb movement disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
combat disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease combat disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
expressive language disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease expressive language disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gender identity disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gender identity disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
purine-pyrimidine metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease purine-pyrimidine metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
amino acid metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease amino acid metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
paranoid personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease paranoid personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schizoaffective disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease schizoaffective disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
sleep disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sleep disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
borderline personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease borderline personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
obsessive-compulsive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease obsessive-compulsive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
articulation disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease articulation disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anxiety disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
psychosexual disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease psychosexual disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
antisocial personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease antisocial personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dependent personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dependent personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
somatoform disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease somatoform disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
steroid inherited metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease steroid inherited metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
generalized anxiety disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease generalized anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
metal metabolism disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease metal metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dissociative disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dissociative disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schizoid personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease schizoid personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
substance-related disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease substance-related disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
physical disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease physical disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
communication disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease communication disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alcohol-induced mental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intermittent explosive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intermittent explosive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
speech disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease speech disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
autistic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease autistic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
attention deficit hyperactivity disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease attention deficit hyperactivity disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bipolar i disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bipolar i disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
inherited metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inherited metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
obsessive-compulsive personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease obsessive-compulsive personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schizophreniform disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease schizophreniform disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alcohol-related neurodevelopmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease alcohol-related neurodevelopmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
developmental disorder of mental health Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease developmental disorder of mental health in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
amnestic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease amnestic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
reading disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease reading disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
writing disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease writing disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
bilirubin metabolic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bilirubin metabolic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
language disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease language disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cognitive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cognitive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
seasonal affective disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease seasonal affective disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
developmental coordination disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease developmental coordination disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
eating disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease eating disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
rumination disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease rumination disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
withdrawal disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease withdrawal disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
impulse control disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease impulse control disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
delusional disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease delusional disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
specific developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease specific developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
drug-induced mental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease drug-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
major depressive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease major depressive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
acute stress disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease acute stress disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hypoactive sexual desire disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypoactive sexual desire disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
pain disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pain disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
phobic disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease phobic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
narcissistic personality disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease narcissistic personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
congenital disorder of glycosylation type i Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital disorder of glycosylation type i in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
adjustment disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adjustment disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gamma-amino butyric acid metabolism disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gamma-amino butyric acid metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
factitious disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease factitious disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atypical depressive disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atypical depressive disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
separation anxiety disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease separation anxiety disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Harmonizome 3.0

AUNX1 Gene

CMTX3 Gene

CMTX2 Gene

HMSN5 Gene

NMSR Gene

SPOAN Gene

HSN1B Gene

HMNJ Gene

HMSNO Gene

Auditory Neuropathy Spectrum Disorder Gene Set

Auditory neuropathy spectrum disorder Gene Set

Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene Set

Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) Gene Set

Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) Gene Set

Obsessive-compulsive disorder or autism spectrum disorder Gene Set

Ataxia Neuropathy Spectrum Disorders Gene Set

Auditory neuropathy, autosomal recessive, 1 Gene Set

Auditory Neuropathy, Autosomal Dominant, 1 Gene Set

auditory neuropathy, autosomal dominant, 1 Gene Set

auditory neuropathy, autosomal recessive, 1 Gene Set

Auditory Neuropathy Gene Set

Auditory Neuropathy, Autosomal Dominant, 1 Gene Set

Auditory Neuropathy And Optic Atrophy Gene Set

Auditory Neuropathy, Nonsyndromic Recessive Gene Set

Autosomal dominant auditory neuropathy 1 Gene Set

Auditory neuropathy Gene Set

Auditory neuropathy-optic atrophy syndrome Gene Set

Autosomal dominant auditory neuropathy Gene Set

Otopalatodigital spectrum disorder Gene Set

NOG-Related-Symphalangism Spectrum Disorder Gene Set

autism spectrum disorder Gene Set

autism spectrum disorder Gene Set

fetal alcohol spectrum disorder Gene Set

autism spectrum disorder Gene Set

autistic spectrum disorder Gene Set

autism spectrum disorder Gene Set

Zellweger Spectrum Disorder Gene Set

Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder Gene Set

Otopalatodigital Spectrum Disorder Gene Set

Synaptic signaling associated with autism spectrum disorder Gene Set

Autism spectrum disorder Gene Set

Otopalatodigital syndrome spectrum disorder Gene Set

Autism spectrum disorder Gene Set

Fetal alcohol spectrum disorder Gene Set

Autism spectrum disorder Gene Set

Otopalatodigital syndrome spectrum disorder Gene Set

Autism spectrum disorder Gene Set

WFS1-spectrum disorder Gene Set

Familial Autism Spectrum Disorder Gene Set

Autism spectrum disorder - epilepsy - arthrogryposis syndrome Gene Set

Autism spectrum disorder due to AUTS2 deficiency Gene Set

ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder Gene Set

GNAO1-related developmental delay-seizures-movement disorder spectrum Gene Set

KIF7-related ciliopathy spectrum disorder Gene Set

ITPR1-associated cerebellar ataxia spectrum disorder Gene Set

NRXN2-related Austism Spectrum Disorder Gene Set

Holoprosencephaly spectrum disorder Gene Set

NRXN2-related autism spectrum disorder Gene Set

Autism spectrum disorder Gene Set

Autism spectrum disorder or schizophrenia Gene Set

Autism spectrum disorder-related traits Gene Set

Restricted and repetitive behaviours in autism spectrum disorder Gene Set

schizophrenia; depressive disorder, major; bipolar disorder; delusional disorder; psychosis Gene Set

anxiety disorder; depressive disorder, major; panic disorder Gene Set

attention deficit disorder; conduct disorder; oppositional defiant disorder Gene Set

conduct disorder; oppositional defiant disorder; antisocial personality disorder Gene Set

alzheimer's disease; attention deficit disorder; conduct disorder; oppositional defiant disorder; dementia, frontotemporal Gene Set

Auditory Processing Disorder, Central Gene Set

Hereditary Motor And Sensory Neuropathy, Type Iic (Disorder) Gene Set

Fetal Alcohol Spectrum Disorders Gene Set

gjb2 mutations--phenotypic spectrum and frequencies of gjb2 mutations Gene Set

cftr mutation spectrum Gene Set

spectrum Gene Set

ASD autism spectrum Gene Set

Zellweger Spectrum Gene Set

Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum Gene Set

Pik3Ca Related Overgrowth Spectrum Gene Set

WFS1-Related Spectrum Disorders Gene Set

TP63-Related Spectrum Disorders Gene Set