| Name |
|---|
HMSN5 GeneHereditary motor and sensory neuropathy V |
NMSR GeneNeuropathy, hereditary motor and sensory, Russe type |
HSN1B GeneHereditary sensory neuropathy, type IB |
HMNJ GeneDistal hereditary motor neuropathy, Jerash type |
HMSNO GeneNeuropathy, hereditary motor and sensory, Okinawa type |
CMTX3 GeneCharcot-Marie-Tooth neuropathy, X-linked 3 (dominant) |
CMTX2 GeneCharcot-Marie-Tooth neuropathy, X-linked 2 (recessive) |
SPOAN Genespastic paraplegia, optic atrophy, and neuropathy |
AUNX1 Geneauditory neuropathy, X-linked recessive 1 |
HPCX Genehereditary prostate cancer, X-linked |
HMN7A GeneMotor neuronopathy, distal hereditary, type VIIA |
HPFH2 Genehereditary persistence of fetal hemoglobin, heterocellular, Indian type |
HHT4 GeneTelangiectasia, hereditary hemorrhagic, type 4 |
HPC5 Geneprostate cancer, hereditary, 5 |
HPC4 GeneProstate cancer, hereditary, 4 |
HPC3 GeneProstate cancer, hereditary, 3 |
HPC7 GeneProstate cancer, hereditary, 7 |
DHS Genedehydrated hereditary stomatocytosis |
GINGF4 Genegingival fibromatosis, hereditary, 4 |
HPC15 GeneProstate cancer, hereditary, 15 |
HPC14 GeneProstate cancer, hereditary, 14 |
HPC10 GeneProstate cancer, hereditary, 10 |
HPC9 GeneProstate cancer, hereditary, 9 |
LMPH1B GeneLymphedema, hereditary, IB |
HEMC Genehemangioma, capillary, hereditary |
HPCX2 GeneProstate cancer, hereditary, X-linked 2 |
PTOS2 GenePtosis, hereditary congenital 2 |
HNB1 Genehereditary neuroblastoma 1 |
ETM3 GeneTremor, hereditary essential, 3 |
HBFQTL2 Genehereditary persistence of fetal hemoglobin, heterocellular |
DKBI GeneDyskeratosis, hereditary benign intraepithelial |
GINGF3 Genegingival fibromatosis, hereditary, 3 |
GINGF2 Genegingival fibromatosis, hereditary, 2 |
CMAL GeneCapillary malformations, hereditary |
MUHH2 GeneHypotrichosis, hereditary, Marie Unna type, 2 |
BP49 GeneBlood pressure QTL 49 |
BP24 GeneBlood pressure QTL 24 |
BP25 GeneBlood pressure QTL 25 |
BP26 GeneBlood pressure QTL 26 |
BP27 GeneBlood pressure QTL 27 |
BP20 GeneBlood pressure QTL 20 |
BP21 GeneBlood pressure QTL 21 |
BP22 GeneBlood pressure QTL 22 |
BP23 GeneBlood pressure QTL 23 |
BP28 GeneBlood pressure QTL 28 |
BP29 GeneBlood pressure QTL 29 |
BP1 GeneBlood pressure QTL 1 |
BP3 GeneBlood pressure QTL 3 |
BP2 GeneBlood pressure QTL 2 |
BP5 GeneBlood pressure QTL 5 |
BP4 GeneBlood pressure QTL 4 |
BP7 GeneBlood pressure QTL 7 |
BP6 GeneBlood pressure QTL 6 |
BP9 GeneBlood pressure QTL 9 |
BP8 GeneBlood pressure QTL 8 |
BP51 GeneBlood pressure QTL 51 |
BP50 GeneBlood pressure QTL 50 |
BP53 GeneBlood pressure QTL 53 |
BP52 GeneBlood pressure QTL 52 |
BP55 GeneBlood pressure QTL 55 |
BP54 GeneBlood pressure QTL 54 |
BP37 GeneBlood pressure QTL 37 |
BP36 GeneBlood pressure QTL 36 |
BP35 GeneBlood pressure QTL 35 |
BP34 GeneBlood pressure QTL 34 |
BP33 GeneBlood pressure QTL 33 |
BP32 GeneBlood pressure QTL 32 |
BP31 GeneBlood pressure QTL 31 |
BP30 GeneBlood pressure QTL 30 |
BP39 GeneBlood pressure QTL 39 |
BP38 GeneBlood pressure QTL 38 |
BP18 GeneBlood pressure QTL 18 |
BP14 GeneBlood pressure QTL 14 |
BP46 GeneBlood pressure QTL 46 |
BP47 GeneBlood pressure QTL 47 |
BP45 GeneBlood pressure QTL 45 |
BP48 GeneBlood pressure QTL 48 |
BP19 GeneBlood pressure QTL 19 |
BP15 GeneBlood pressure QTL 15 |
BP17 GeneBlood pressure QTL 17 |
BP16 GeneBlood pressure QTL 16 |
BP11 GeneBlood pressure QTL 11 |
BP10 GeneBlood pressure QTL 10 |
BP13 GeneBlood pressure QTL 13 |
BP12 GeneBlood pressure QTL 12 |
Hereditary neuropathy with liability to pressure palsies Gene SetFrom 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 neuropathy with liability to pressure palsies Gene SetFrom 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. |
Hereditary liability to pressure palsies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary liability to pressure palsies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Liability To Pressure Palsies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Liability To Pressure Palsies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary liability to pressure palsies Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary liability to pressure palsies phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
neuropathy, recurrent, with pressure palsies Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, recurrent, with pressure palsies phenotype from the curated OMIM Gene-Disease Associations dataset. |
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene SetFrom 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. |
gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastrointestinal neoplasms; hht - hereditary hemorrhagic telangiectasia; intestinal polyposis; neoplastic syndromes, hereditary; telangiectasia, hereditary hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
liability Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term liability in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Cranial Nerve Palsies Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cranial Nerve Palsies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Systolic blood pressure and diastolic blood pressure (bivariate analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure and diastolic blood pressure (bivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
White coat effect (clinic systolic blood pressure minus ambulatory systolic blood pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White coat effect (clinic systolic blood pressure minus ambulatory systolic blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
White coat effect (clinic diastolic blood pressure minus ambulatory diastolic blood pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White coat effect (clinic diastolic blood pressure minus ambulatory diastolic blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive Gene SetFrom 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. |
Neuropathy hereditary sensory and autonomic type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy hereditary sensory and autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Neuropathy, hereditary motor and sensory, Okinawa type Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IF phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary motor and sensory neuropathy with optic atrophy Gene SetFrom 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 SetFrom 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. |
NEUROPATHY, HEREDITARY SENSORY, TYPE IC Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the NEUROPATHY, HEREDITARY SENSORY, TYPE IC phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked hereditary motor and sensory neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary sensory and autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Sensory and Motor Neuropathy Gene SetFrom 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 SetFrom 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. |
Neuropathy, hereditary motor and sensory, Russe type Gene SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type IIA from the curated CTD Gene-Disease Associations dataset. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene SetFrom 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 SetFrom 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. |
Hereditary Motor And Sensory Neuropathy VI Gene SetFrom 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 SetFrom 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 SetFrom 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. |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene SetFrom 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. |
Neuropathy, Hereditary Sensory, with Spastic Paraplegia, Autosomal Recessive Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Neuropathy, hereditary motor and sensory, LOM type Gene SetFrom 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. |
hereditary sensory neuropathy Gene SetFrom 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. |
hereditary sensory neuropathy Gene SetFrom 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. |
leber hereditary optic neuropathy Gene SetFrom 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 SetFrom 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, hereditary motor and sensory Gene SetFrom 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. |
leber's hereditary optic neuropathy Gene SetFrom 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. |
charcot-marie-tooth disease; hereditary sensory and motor neuropathy Gene SetFrom 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. |
Hereditary Sensory and Motor Neuropathy Gene SetFrom 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. |
?neuropathy, hereditary sensory and autonomic, type vi Gene SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, with spastic paraplegia phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory and autonomic, type ia Gene SetFrom 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 SetFrom 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 SetFrom 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, hereditary sensory, type iic Gene SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type iib phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, jerash type Gene SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy v phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory, type ie Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory, type ib phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary motor and sensory, russe type Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary motor and sensory, russe type phenotype from the curated OMIM Gene-Disease Associations dataset. |
hereditary motor and sensory neuropathy, proximal type Gene SetFrom 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 SetFrom 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 SetFrom 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, hereditary sensory and autonomic, type vii Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type vii phenotype from the curated OMIM Gene-Disease Associations dataset. |
hereditary motor and sensory neuropathy vi Gene SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, hereditary sensory and autonomic, type v Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, hereditary sensory and autonomic, type v phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type iib Gene SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset. |
Hereditary Motor And Sensory Neuropathy Gene SetFrom 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. |
Hereditary Sensory Autonomic Neuropathy Gene SetFrom 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 SetFrom 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. |
Sensory Neuropathy, Hereditary Gene SetFrom 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. |
Distal Hereditary Motor Neuropathy Gene SetFrom 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. |
Hereditary Sensory And Autonomic Neuropathy Gene SetFrom 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 SetFrom 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. |
Hereditary Motor And Sensory Neuropathy, Type Iic (Disorder) Gene SetFrom 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. |
Hereditary Peripheral Neuropathy Gene SetFrom 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. |
Hereditary And Idiopathic Neuropathy, Unspecified Gene SetFrom 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. |
Leber hereditary optic neuropathy Gene SetFrom 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. |
Hereditary sensory and autonomic neuropathy type 2 Gene SetFrom 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 SetFrom 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. |
Hereditary sensory and autonomic neuropathy type 1 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Leber hereditary optic neuropathy and dystonia Gene SetFrom 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. |
Leber hereditary optic neuropathy Gene SetFrom 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. |
Hereditary sensory neuropathy Gene SetFrom 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. |
Hereditary sensory and autonomic neuropathy type 2A Gene SetFrom 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 SetFrom 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. |
Hereditary sensory and autonomic neuropathy type 2 Gene SetFrom 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 SetFrom 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. |
Hereditary sensory neuropathy type 2C Gene SetFrom 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. |
Hereditary sensory neuropathy type 1E Gene SetFrom 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. |
Hereditary sensory and autonomic neuropathy type 6 Gene SetFrom 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. |
Hereditary sensory and autonomic neuropathy type 5 Gene SetFrom 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. |
Hereditary sensory and autonomic neuropathy type 1C Gene SetFrom 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. |
Hereditary sensory and autonomic neuropathy type 2B Gene SetFrom 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. |
Hereditary sensory neuropathy type 1D Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Hereditary sensory neuropathy type 4 Gene SetFrom 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. |
Hereditary sensory and autonomic neuropathy Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary motor and sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal hereditary motor neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal hereditary motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary sensory neuropathy-deafness-dementia syndrome Gene SetFrom 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. |
Autosomal dominant hereditary axonal motor and sensory neuropathy Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary sensorimotor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary peripheral neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Leber-like hereditary optic neuropathy Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Leber hereditary optic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Hereditary diffuse gastric cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Hereditary diffuse gastric cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; hereditary nonpolyposis colorectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms; hereditary nonpolyposis colorectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies, hereditary; hereditary corneal dystrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms, second primary; rectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms, second primary; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; microsatellite instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary nephritis; nephritis, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary nephritis; nephritis, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; hereditary corneal dystrophy; hernia, abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Blood Pressure Determination Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Blood Pressure Determination in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Blood Pressure Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Blood Pressure in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
high pressure neurological syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease high pressure neurological syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
normal pressure hydrocephalus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease normal pressure hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
blood pressure, arterial; heart rate; orthostatic intolerance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; heart rate; orthostatic intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
baroreflex and blood pressure regulation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease baroreflex and blood pressure regulation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure; aldosterone; glomerular filtration rate; renal plasma flow Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure; aldosterone; glomerular filtration rate; renal plasma flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, oxidative stress levels in blood Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, oxidative stress levels in blood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; left ventricular function; blood pressure; left ventricular structure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; left ventricular function; blood pressure; left ventricular structure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
triglycerides; blood pressure, arterial; antioxidant activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease triglycerides; blood pressure, arterial; antioxidant activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure; heart rate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure; heart rate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
left ventricular hypertrophy; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease left ventricular hypertrophy; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; carotid atherosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; carotid atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anxiety disorder; blood pressure, arterial; memory impairment Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anxiety disorder; blood pressure, arterial; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; diabetes, type 2; blood pressure, arterial; liver disease; periodontitis; acenocoumarol response; acetaldehyde; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; diabetes, type 2; blood pressure, arterial; liver disease; periodontitis; acenocoumarol response; acetaldehyde; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; arterial wall changes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; arterial wall changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; triglycerides; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; triglycerides; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; left ventricular mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; left ventricular mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; triglycerides; hypertension; blood pressure, arterial; potassium; urea Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; triglycerides; hypertension; blood pressure, arterial; potassium; urea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
systolic blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease systolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipids; blood pressure; atherosclerosis, carotid Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipids; blood pressure; atherosclerosis, carotid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure determination Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure determination in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
macroangiopathy and blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease macroangiopathy and blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, ldl; blood pressure, arterial; nitric oxide production; salt sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, ldl; blood pressure, arterial; nitric oxide production; salt sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ace concentration and blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ace concentration and blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; cholesterol, ldl; glucose tolerance; blood pressure, arterial; glycosylated hemoglobin a1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; cholesterol, ldl; glucose tolerance; blood pressure, arterial; glycosylated hemoglobin a1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
progression of carotid atherosclerosis blood pressure and serum lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease progression of carotid atherosclerosis blood pressure and serum lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; blood pressure, arterial; stroke; longevity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; blood pressure, arterial; stroke; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adiposity and blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adiposity and blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; sodium hemostatis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; sodium hemostatis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; renin activity; aldosterone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; renin activity; aldosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; blood pressure, arterial; sleep apnea Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; blood pressure, arterial; sleep apnea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
preeclampsia; blood pressure; endothelin-1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease preeclampsia; blood pressure; endothelin-1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; adiponectin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; adiponectin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; triglycerides; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; triglycerides; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; blood pressure, arterial; acetaldehyde; lipid peroxide Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; blood pressure, arterial; acetaldehyde; lipid peroxide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
nephropathy, diabetic; blood pressure, arterial; proteinuria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease nephropathy, diabetic; blood pressure, arterial; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; cystic fibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; lipids; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; lipids; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol, hdl; blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, hdl; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; insulin; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial diabetes, type 2 glucose insulin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial diabetes, type 2 glucose insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased blood pressure and plasma triglycerides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease decreased blood pressure and plasma triglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
central pulse pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease central pulse pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pulse pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pulse pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; heart rate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; heart rate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
higher blood pressure after hospitalization in normotensi Gene SetFrom GAD Gene-Disease Associations genes associated with the disease higher blood pressure after hospitalization in normotensi in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; nitric oxide production; salt sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; nitric oxide production; salt sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sleep disorders; body mass; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; atherosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure phenotypes. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure phenotypes. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure; hyperlipidemia, familial combined Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure; aldosterone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure; aldosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 1; blood pressure, arterial; nephropathy in other diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 1; blood pressure, arterial; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diastolic blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diastolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
arthritis; cholesterol, hdl; diabetes, type 2; osteoarthritis; blood pressure, arterial; liver disease; acetaldehyde; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease arthritis; cholesterol, hdl; diabetes, type 2; osteoarthritis; blood pressure, arterial; liver disease; acetaldehyde; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood pressure, arterial; heart rate; adrenaline; coronary flow velocity; ecg; noradrenaline Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood pressure, arterial; heart rate; adrenaline; coronary flow velocity; ecg; noradrenaline in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; diabetes, type 2; blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; diabetes, type 2; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; diabetes, type 2; insulin; glucose; insulin resistance; pc-1 protein content; systolic blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; diabetes, type 2; insulin; glucose; insulin resistance; pc-1 protein content; systolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol; insulin; obesity; blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol; insulin; obesity; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
elevated blood pressure and personality disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease elevated blood pressure and personality disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; triglycerides; blood pressure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; triglycerides; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alcohol abuse; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alcohol abuse; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass index, blood pressure and cholesterol Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass index, blood pressure and cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pressure Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term pressure in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Gata-6_KO_GDS4782_330_mouse_Adult heart during pressure overload Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Gata-6_KO_GDS4782_330_mouse_Adult heart during pressure overload gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
Gata-4_KO_GDS4782_329_mouse_Adult heart during pressure overload Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the Gata-4_KO_GDS4782_329_mouse_Adult heart during pressure overload gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
negative regulation of heart rate involved in baroreceptor response to increased systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of heart rate involved in baroreceptor response to increased systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
norepinephrine-epinephrine vasoconstriction involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the norepinephrine-epinephrine vasoconstriction involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
vasodilation of artery involved in baroreceptor response to increased systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the vasodilation of artery involved in baroreceptor response to increased systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to hydrostatic pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to hydrostatic pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
angiotensin mediated vasoconstriction involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the angiotensin mediated vasoconstriction involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
pressure natriuresis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the pressure natriuresis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure mediated by a chemical signal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure mediated by a chemical signal biological process from the curated GO Biological Process Annotations 2015 dataset. |
renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure by vasopressin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by vasopressin biological process from the curated GO Biological Process Annotations 2015 dataset. |
vasodilation by angiotensin involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the vasodilation by angiotensin involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
vasodilation by acetylcholine involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the vasodilation by acetylcholine involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure by atrial natriuretic peptide Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by atrial natriuretic peptide biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
vasoconstriction of artery involved in ischemic response to lowering of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the vasoconstriction of artery involved in ischemic response to lowering of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of the force of heart contraction involved in baroreceptor response to increased systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of the force of heart contraction involved in baroreceptor response to increased systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
vasodilation by norepinephrine-epinephrine involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the vasodilation by norepinephrine-epinephrine involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure by circulatory renin-angiotensin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by circulatory renin-angiotensin biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to hydrostatic pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to hydrostatic pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure by endothelin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by endothelin biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure by renin-angiotensin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by renin-angiotensin biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure by hormone Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by hormone biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
neurological system process involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the neurological system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure by ischemic conditions Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by ischemic conditions biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lung blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lung blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of systemic arterial blood pressure by baroreceptor feedback Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of systemic arterial blood pressure by baroreceptor feedback biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
vasoconstriction of artery involved in baroreceptor response to lowering of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the vasoconstriction of artery involved in baroreceptor response to lowering of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
renal system process involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2015 genes participating in the renal system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2015 dataset. |
Blood pressure measurement (high sodium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure measurement (high sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Diastolic blood pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Diastolic blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Triglycerides-Blood Pressure (TG-BP) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Triglycerides-Blood Pressure (TG-BP) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Blood pressure measurement (cold pressor test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure measurement (cold pressor test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Diastolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Diastolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Systolic blood pressure in sickle cell anemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Systolic blood pressure in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Blood pressure measurement (high sodium and potassium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure measurement (high sodium and potassium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Blood pressure (age interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Obesity and blood pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Obesity and blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Blood pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Intraocular pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Intraocular pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Blood pressure measurement (low sodium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Blood pressure measurement (low sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Systolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Systolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Systolic blood pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Systolic blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Mean arterial pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Mean arterial pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormal intraocular pressure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
increased intraocular pressure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the increased intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
elevated systolic blood pressure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the elevated systolic blood pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
low-to-normal blood pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the low-to-normal blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
normal pressure hydrocephalus Gene SetFrom HPO Gene-Disease Associations genes associated with the normal pressure hydrocephalus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated diastolic blood pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated diastolic blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated systolic blood pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated systolic blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated right atrial pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated right atrial pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased intracranial pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the increased intracranial pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated mean arterial pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated mean arterial pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased intraocular pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the increased intraocular pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of intracranial pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of intracranial pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
elevated pulmonary artery pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the elevated pulmonary artery pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal intraocular pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal intraocular pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Hydrocephalus, Normal Pressure Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hydrocephalus, Normal Pressure phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
decreased systemic arterial blood pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased left ventricle developed pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased left ventricle developed pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulse pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulse pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased systemic arterial blood pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased left ventricle systolic pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased left ventricle systolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal systemic arterial blood pressure regulation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal systemic arterial blood pressure regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pulse pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pulse pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased right ventricle systolic pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased right ventricle systolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased systemic arterial systolic blood pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased systemic arterial systolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased right ventricle peak pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased right ventricle peak pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased left ventricle developed pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased left ventricle developed pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart right ventricle pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart right ventricle pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased left ventricle diastolic pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased left ventricle diastolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart ventricle pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart ventricle pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased left ventricle systolic pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased left ventricle systolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased left ventricle diastolic pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased left ventricle diastolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased mean systemic arterial blood pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased mean systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased pulse pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased pulse pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased systemic arterial diastolic blood pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased systemic arterial diastolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased mean systemic arterial blood pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased mean systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal systemic arterial blood pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart left ventricle pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart left ventricle pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased systemic arterial systolic blood pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased systemic arterial systolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood pressure regulation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood pressure regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased systemic arterial diastolic blood pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased systemic arterial diastolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased pulmonary artery pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased pulmonary artery pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circadian regulation of systemic arterial blood pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circadian regulation of systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased right ventricle systolic pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased right ventricle systolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intraocular pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intraocular pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pulmonary pressure Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pulmonary pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[blood pressure regulation qtl] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [blood pressure regulation qtl] phenotype from the curated OMIM Gene-Disease Associations dataset. |
Intraocular Pressure Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Intraocular Pressure Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pressure Ulcer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pressure Ulcer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Idiopathic Normal Pressure Hydrocephalus (Inph) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Normal Pressure Hydrocephalus (Inph) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pressure Ulcer Stage 4 (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pressure Ulcer Stage 4 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
(Idiopathic) Normal Pressure Hydrocephalus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease (Idiopathic) Normal Pressure Hydrocephalus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Systolic Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Systolic Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Diastolic Blood Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diastolic Blood Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Diastolic Blood Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Diastolic Blood Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Mean Arterial Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Mean Arterial Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Systolic Blood Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Systolic Blood Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Blood Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blood Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mean Blood Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mean Blood Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Diastolic Blood Pressure Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diastolic Blood Pressure Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Pulse Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Pulse Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Systolic Blood Pressure Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Systolic Blood Pressure Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ankle Brachial Pressure Index (Observable Entity) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ankle Brachial Pressure Index (Observable Entity) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Right Atrial Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Right Atrial Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Raised Jugular Venous Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Raised Jugular Venous Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Elevated Pulmonary Artery Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elevated Pulmonary Artery Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low-To-Normal Blood Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low-To-Normal Blood Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sinus Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sinus Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Physiologic Intraocular Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Physiologic Intraocular Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Chest Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chest Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Asymmetry Of Intraocular Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Asymmetry Of Intraocular Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Reduced Maximal Inspiratory Pressure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Reduced Maximal Inspiratory Pressure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
negative regulation of blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
acetylcholine-mediated vasodilation involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the acetylcholine-mediated vasodilation involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure by endothelin Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure by endothelin biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure by renin-angiotensin Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure by renin-angiotensin biological process from the curated GO Biological Process Annotations 2023 dataset. |
nervous system process involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the nervous system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure by ischemic conditions Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure by ischemic conditions biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure mediated by a chemical signal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure mediated by a chemical signal biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to hydrostatic pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to hydrostatic pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure by circulatory renin-angiotensin Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure by circulatory renin-angiotensin biological process from the curated GO Biological Process Annotations 2023 dataset. |
pressure natriuresis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the pressure natriuresis biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lung blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lung blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure by atrial natriuretic peptide Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure by atrial natriuretic peptide biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure by vasopressin Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure by vasopressin biological process from the curated GO Biological Process Annotations 2023 dataset. |
renal system process involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the renal system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure by acetylcholine Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure by acetylcholine biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure by hormone Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure by hormone biological process from the curated GO Biological Process Annotations 2023 dataset. |
renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2023 genes participating in the renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of systemic arterial blood pressure by norepinephrine-epinephrine Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of systemic arterial blood pressure by norepinephrine-epinephrine biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of blood pressure by epinephrine-norepinephrine Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of blood pressure by epinephrine-norepinephrine biological process from the curated GO Biological Process Annotations 2023 dataset. |
decreased systemic arterial blood pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased systemic arterial blood pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased systemic arterial blood pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased systemic arterial blood pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal systemic arterial blood pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal systemic arterial blood pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pulmonary pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pulmonary pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased mean systemic arterial blood pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased mean systemic arterial blood pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal heart right ventricle pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart right ventricle pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased left ventricle systolic pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased left ventricle systolic pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased systemic arterial diastolic blood pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased systemic arterial diastolic blood pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased systemic arterial systolic blood pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased systemic arterial systolic blood pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circadian regulation of systemic arterial blood pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circadian regulation of systemic arterial blood pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased left ventricle systolic pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased left ventricle systolic pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased left ventricle diastolic pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased left ventricle diastolic pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased systemic arterial systolic blood pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased systemic arterial systolic blood pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased systemic arterial diastolic blood pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased systemic arterial diastolic blood pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased mean systemic arterial blood pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased mean systemic arterial blood pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intraocular pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intraocular pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased right ventricle systolic pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased right ventricle systolic pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased left ventricle developed pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased left ventricle developed pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal blood pressure regulation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood pressure regulation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal systemic arterial blood pressure regulation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal systemic arterial blood pressure regulation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal heart left ventricle pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart left ventricle pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased right ventricle peak pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased right ventricle peak pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal heart ventricle pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart ventricle pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased right ventricle systolic pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased right ventricle systolic pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased left ventricle developed pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased left ventricle developed pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pulse pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pulse pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased left ventricle diastolic pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased left ventricle diastolic pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased pulse pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased pulse pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pulmonary artery pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pulmonary artery pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased pulmonary artery pressure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased pulmonary artery pressure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal renal arterial blood pressure regulation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal renal arterial blood pressure regulation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
negative regulation of blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
acetylcholine-mediated vasodilation involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the acetylcholine-mediated vasodilation involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure by endothelin Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by endothelin biological process from the curated GO Biological Process Annotations 2025 dataset. |
nervous system process involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the nervous system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure by renin-angiotensin Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by renin-angiotensin biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure by ischemic conditions Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by ischemic conditions biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure mediated by a chemical signal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure mediated by a chemical signal biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to hydrostatic pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to hydrostatic pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure by circulatory renin-angiotensin Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by circulatory renin-angiotensin biological process from the curated GO Biological Process Annotations 2025 dataset. |
pressure natriuresis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the pressure natriuresis biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lung blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lung blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure by atrial natriuretic peptide Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by atrial natriuretic peptide biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure by vasopressin Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by vasopressin biological process from the curated GO Biological Process Annotations 2025 dataset. |
norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure by carotid body chemoreceptor signaling Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by carotid body chemoreceptor signaling biological process from the curated GO Biological Process Annotations 2025 dataset. |
renal system process involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the renal system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure by acetylcholine Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by acetylcholine biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure by hormone Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by hormone biological process from the curated GO Biological Process Annotations 2025 dataset. |
renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure Gene SetFrom GO Biological Process Annotations 2025 genes participating in the renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of systemic arterial blood pressure by norepinephrine-epinephrine Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of systemic arterial blood pressure by norepinephrine-epinephrine biological process from the curated GO Biological Process Annotations 2025 dataset. |
Normal pressure hydrocephalus Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Normal pressure hydrocephalus in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
High pressure neurological syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease High pressure neurological syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Elevated systolic blood pressure Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Elevated systolic blood pressure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Elevated diastolic blood pressure Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Elevated diastolic blood pressure phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Normal pressure hydrocephalus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Normal pressure hydrocephalus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Diastolic blood pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x educational attainment (some college) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x educational attainment (some college) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x educational attainment (graduated college) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x educational attainment (graduated college) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x educational attainment (graduated college) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x educational attainment (graduated college) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure x educational attainment (some college) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure x educational attainment (some college) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure x educational attainment (graduated college) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure x educational attainment (graduated college) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure x educational attainment (some college) interaction (2df) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure x educational attainment (some college) interaction (2df) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Change in intraocular pressure in response to steroid treatment (triamcinolone acetonide) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Change in intraocular pressure in response to steroid treatment (triamcinolone acetonide) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure response to hydrochlorothiazide in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure response to hydrochlorothiazide in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure response to hydrochlorothiazide in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure response to hydrochlorothiazide in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intraocular pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intraocular pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Glaucoma (high intraocular pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glaucoma (high intraocular pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure (cigarette smoking interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure (cigarette smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure (long-term average) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure (long-term average) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure (long-term average) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure (long-term average) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure (long-term average) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure (long-term average) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x sodium interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x sodium interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x sodium interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x sodium interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x sodium interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x sodium interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure x sodium interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure x sodium interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure change trajectory Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure change trajectory phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x smoking status (ever vs never) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x smoking status (ever vs never) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x smoking status (current vs non-current) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x smoking status (current vs non-current) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x smoking status (ever vs never) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x smoking status (ever vs never) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x smoking status (ever vs never) interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x smoking status (ever vs never) interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure (dietary potassium intake interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure (dietary potassium intake interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure response to thiazide and thiazide-like diuretics in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure response to thiazide and thiazide-like diuretics in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure response to thiazide and thiazide-like diuretics in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure response to thiazide and thiazide-like diuretics in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x quantitative lifestyle risk score interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x quantitative lifestyle risk score interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x quantitative lifestyle risk score interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x quantitative lifestyle risk score interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x dichotomous lifestyle risk score interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x dichotomous lifestyle risk score interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x dichotomous lifestyle risk score interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x dichotomous lifestyle risk score interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x quantitative lifestyle risk score interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x quantitative lifestyle risk score interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x quantitative lifestyle risk score interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x quantitative lifestyle risk score interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x dichotomous lifestyle risk score interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x dichotomous lifestyle risk score interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x dichotomous lifestyle risk score interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x dichotomous lifestyle risk score interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure night-to-day ratio in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure night-to-day ratio in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure night-to-day ratio in hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure night-to-day ratio in hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intraocular pressure and central corneal thickness (multi-trait analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intraocular pressure and central corneal thickness (multi-trait analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and systolic blood pressure (bivariate analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and systolic blood pressure (bivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and diastolic blood pressure (bivariate analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and diastolic blood pressure (bivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Waist-hip ratio and systolic blood pressure (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-hip ratio and systolic blood pressure (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body mass index and systole blood pressure (pairwise) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index and systole blood pressure (pairwise) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure (education interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure (education interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure (education interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure (education interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Chronic obstructive pulmonary disease or high blood pressure (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Chronic obstructive pulmonary disease or high blood pressure (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Rapid response to perioperative phenylephrine (change in mean arterial pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Rapid response to perioperative phenylephrine (change in mean arterial pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Rapid response to perioperative phenylephrine (change in systolic blood pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Rapid response to perioperative phenylephrine (change in systolic blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Glaucoma (low intraocular pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glaucoma (low intraocular pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure (smoking interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure (smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure (alcohol consumption interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure in young-onset hypertension Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure in young-onset hypertension phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure (anthropometric measures interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure (anthropometric measures interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure (age interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure measurement (cold pressor test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure measurement (cold pressor test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure measurement (low sodium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure measurement (low sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure measurement (high sodium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure measurement (high sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure measurement (high sodium and potassium intervention) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure measurement (high sodium and potassium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure in sickle cell anemia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure (baseline) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure (baseline) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intraocular pressure (corneal compensated) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intraocular pressure (corneal compensated) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intraocular pressure (Goldman correlated) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intraocular pressure (Goldman correlated) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Triglycerides-Blood Pressure (TG-BP) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Triglycerides-Blood Pressure (TG-BP) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pulse pressure x alcohol consumption (light vs heavy) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pulse pressure x alcohol consumption (light vs heavy) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blood pressure traits (multi-trait analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blood pressure traits (multi-trait analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x smoking status (current vs non-current) interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x smoking status (current vs non-current) interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Systolic blood pressure x smoking status (current vs non-current) interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Systolic blood pressure x smoking status (current vs non-current) interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x smoking status (current vs non-current) interaction (1df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x smoking status (current vs non-current) interaction (1df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Uncontrolled blood pressure in combination therapy (beta blocker and thiazide diuretic) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Uncontrolled blood pressure in combination therapy (beta blocker and thiazide diuretic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure in combination therapy (beta blocker and thiazide diuretic) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure in combination therapy (beta blocker and thiazide diuretic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure (cigarette smoking interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure (cigarette smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Diastolic blood pressure x alcohol consumption interaction (2df test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Diastolic blood pressure x alcohol consumption interaction (2df test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Multiple sclerosis and systolic blood pressure (pleiotropy) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple sclerosis and systolic blood pressure (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to beta blocker use in hypertension (systolic blood pressure) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to beta blocker use in hypertension (systolic blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Trifunctional protein deficiency with myopathy and neuropathy Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Giant axonal neuropathy, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Auditory neuropathy, autosomal recessive, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Auditory neuropathy, autosomal recessive, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene SetFrom 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. |
Spinocerebellar ataxia autosomal recessive with axonal neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Spinocerebellar ataxia autosomal recessive with axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
46,XY gonadal dysgenesis, partial, with minifascicular neuropathy Gene SetFrom 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, congenital hypomyelinating, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom 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 SetFrom 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. |
Trifunctional Protein Deficiency With Myopathy And Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sciatic Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy Gene SetFrom 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. |
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sensorimotor neuropathy with ataxia, autosomal dominant from the curated CTD Gene-Disease Associations dataset. |
46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy Gene SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Giant Axonal Neuropathy from the curated CTD Gene-Disease Associations dataset. |
Auditory Neuropathy, Autosomal Dominant, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Auditory Neuropathy, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset. |
Optic Neuropathy, Ischemic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Neuropathy, Ischemic from the curated CTD Gene-Disease Associations dataset. |
Inherited Peripheral Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
neuropathy Gene SetFrom 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 SetFrom 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. |
inflammatory and toxic neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
charcot-marie-tooth neuropathy type 1b Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
neuropathy, charcot-marie-tooth Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
dementia; neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom GWASdb SNP-Phenotype Associations genes associated with the peripheral neuropathy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
sensory neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Alcoholic Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom MPO Gene-Phenotype Associations gene mutations causing the optic neuropathy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
neuromyotonia and axonal neuropathy, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuromyotonia and axonal neuropathy, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, congenital hypomyelinating, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, congenital hypomyelinating, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
giant axonal neuropathy-1 Gene SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, motor and sensory, russe type phenotype from the curated OMIM Gene-Disease Associations dataset. |
auditory neuropathy, autosomal dominant, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the auditory neuropathy, autosomal dominant, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the 46xy partial gonadal dysgenesis, with minifascicular neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
congenital cataracts, facial dysmorphism, and neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
deafness, autosomal dominant, with peripheral neuropathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the deafness, autosomal dominant, with peripheral neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, inflammatory demyelinating Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, inflammatory demyelinating phenotype from the curated OMIM Gene-Disease Associations dataset. |
cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene SetFrom 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. |
?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset. |
leukoencephalopathy with dystonia and motor neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom OMIM Gene-Disease Associations genes associated with the ?giant axonal neuropathy 2, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
auditory neuropathy, autosomal recessive, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the auditory neuropathy, autosomal recessive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Axonal Neuropathy Gene SetFrom 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 SetFrom 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. |
Peripheral Axonal Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Visceral Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Auditory Neuropathy Gene SetFrom 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 Spectrum Disorder Gene SetFrom 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. |
Axonal Sensorimotor Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Periodic Paralysis With Later-Onset Distal Motor Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy Gene SetFrom 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. |
Auditory Neuropathy, Autosomal Dominant, 1 Gene SetFrom 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. |
Distal Peripheral Sensory Neuropathy Gene SetFrom 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 SetFrom 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. |
Autoimmune Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Auditory Neuropathy And Optic Atrophy Gene SetFrom 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. |
Adult Polyglucosan Body Neuropathy Gene SetFrom 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. |
Anterior Ischemic Optic Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Peripheral Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Auditory Neuropathy, Nonsyndromic Recessive Gene SetFrom 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. |
Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 Setproteins participating in the Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN) pathway from the Reactome Pathways 2024 dataset. |
Neuropathy Gene SetFrom 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. |
Spinocerebellar ataxia with axonal neuropathy 2 Gene SetFrom 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 SetFrom 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. |
Brachial plexus neuropathy Gene SetFrom 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 SetFrom 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. |
Neuropathy Gene SetFrom 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 SetFrom 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. |
Diabetic neuropathy Gene SetFrom 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. |
Axonal neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Autonomic neuropathy Gene SetFrom 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. |
non-arteritic anterior ischemic optic neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Autosomal dominant auditory neuropathy 1 Gene SetFrom 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. |
Spinocerebellar ataxia with axonal neuropathy 2 Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Sciatic neuropathy Gene SetFrom 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. |
Nutritional optic neuropathy Gene SetFrom 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 SetFrom 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. |
Uremic neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Peroneal neuropathy Gene SetFrom 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. |
Agenesis of the corpus callosum with peripheral neuropathy Gene SetFrom 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. |
Ulnar neuropathy Gene SetFrom 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. |
Ischemic neuropathy Gene SetFrom 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 SetFrom 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. |
Femoral neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral axonal neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sensorimotor neuropathy Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Auditory neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Charcot-Marie-Tooth Neuropathy Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sensory ataxic neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Dejerine-sottas neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Dejerine-sottas neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Auditory neuropathy spectrum disorder Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Small fiber neuropathy Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Visceral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
GARS-Associated Axonal Neuropathy Gene SetFrom 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 SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Ataxia Neuropathy Spectrum Disorders Gene SetFrom 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-optic atrophy syndrome Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant auditory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary acrodermatitis enteropathica Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary acrodermatitis enteropathica phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prostate cancer, hereditary, 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prostate cancer, hereditary, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Telangiectasia, hereditary hemorrhagic, type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Telangiectasia, hereditary hemorrhagic, type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Lynch syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary neutrophilia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary neutrophilia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Facial paresis, hereditary congenital, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Facial paresis, hereditary congenital, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary sideroblastic anemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary sideroblastic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary hemochromatosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary hemochromatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary C1 esterase inhibitor deficiency - dysfunctional factor phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary hemorrhagic telangiectasia type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary hemorrhagic telangiectasia type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy 2D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Paraganglioma-Pheochromocytoma Syndromes Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paraganglioma-Pheochromocytoma Syndromes phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary fructosuria Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary fructosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary neuralgic amyotrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary neuralgic amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lynch syndrome:Hereditary cancer-predisposing syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lynch syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Dominant hereditary optic atrophy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor II deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor II deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary diffuse gastric cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary diffuse gastric cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Alpha-fetoprotein, hereditary persistence of Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Alpha-fetoprotein, hereditary persistence of phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prostate cancer, hereditary, 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prostate cancer, hereditary, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary lymphedema type I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary lymphedema type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary diffuse leukoencephalopathy with spheroids Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary diffuse leukoencephalopathy with spheroids phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy with lactic acidosis, hereditary Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy with lactic acidosis, hereditary phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tremor, hereditary essential, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tremor, hereditary essential, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary Paragangliomas and Pheochromocytomas Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary Paragangliomas and Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor IX deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor IX deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lymphedema, hereditary, ic Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lymphedema, hereditary, ic phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lymphedema, hereditary, id Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lymphedema, hereditary, id phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary myopathy with early respiratory failure Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary myopathy with early respiratory failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 5B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary gingival fibromatosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary gingival fibromatosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor XI deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor XI deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary leiomyomatosis and renal cell cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary leiomyomatosis and renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary angioedema type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary angioedema type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Marie Unna hereditary hypotrichosis 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Marie Unna hereditary hypotrichosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary pyropoikilocytosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary pyropoikilocytosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 7B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperekplexia hereditary Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperekplexia hereditary phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary insensitivity to pain with anhidrosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary insensitivity to pain with anhidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Infantile-onset ascending hereditary spastic paralysis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary hemorrhagic telangiectasia type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary hemorrhagic telangiectasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cancer-predisposing syndrome:Erythrocytosis, familial, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prostate cancer, hereditary, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prostate cancer, hereditary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prostate cancer, hereditary, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Prostate cancer, hereditary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary pancreatitis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary pancreatitis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary factor VIII deficiency disease Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary factor VIII deficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary cerebral amyloid angiopathy, Icelandic type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary cerebral amyloid angiopathy, Icelandic type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary nonpolyposis colorectal cancer type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary nonpolyposis colorectal cancer type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary nonpolyposis colorectal cancer type 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary nonpolyposis colorectal cancer type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hereditary nonpolyposis colorectal cancer type 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hereditary nonpolyposis colorectal cancer type 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Prostate Cancer, Hereditary, 15 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 15 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 9 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 8 from the curated CTD Gene-Disease Associations dataset. |
Hereditary renal agenesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary renal agenesis from the curated CTD Gene-Disease Associations dataset. |
Dyskeratosis, Hereditary Benign Intraepithelial Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dyskeratosis, Hereditary Benign Intraepithelial from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 14 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 14 from the curated CTD Gene-Disease Associations dataset. |
Tremor hereditary essential, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tremor hereditary essential, 1 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 11 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 13 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 12 from the curated CTD Gene-Disease Associations dataset. |
Hyperexplexia hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperexplexia hereditary from the curated CTD Gene-Disease Associations dataset. |
Angioedemas, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Angioedemas, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophy, Hereditary, Leber Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset. |
Eye Diseases, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Eye Diseases, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Facial paresis, hereditary, congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Facial paresis, hereditary, congenital from the curated CTD Gene-Disease Associations dataset. |
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cerebral hemorrhage with amyloidosis, hereditary, Dutch type from the curated CTD Gene-Disease Associations dataset. |
Thrombophilia, hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia, hereditary from the curated CTD Gene-Disease Associations dataset. |
Elliptocytosis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Elliptocytosis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Hyperferritinemia, hereditary, with congenital cataracts Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperferritinemia, hereditary, with congenital cataracts from the curated CTD Gene-Disease Associations dataset. |
Hypophosphatemic Rickets with Hypercalciuria, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypophosphatemic Rickets with Hypercalciuria, Hereditary from the curated CTD Gene-Disease Associations dataset. |
PROSTATE CANCER, HEREDITARY, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PROSTATE CANCER, HEREDITARY, 1 from the curated CTD Gene-Disease Associations dataset. |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset. |
Tremor hereditary essential, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Tremor hereditary essential, 2 from the curated CTD Gene-Disease Associations dataset. |
Polyposis Syndrome, Hereditary Mixed, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyposis Syndrome, Hereditary Mixed, 2 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 10 from the curated CTD Gene-Disease Associations dataset. |
Osteolysis hereditary multicentric Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Osteolysis hereditary multicentric from the curated CTD Gene-Disease Associations dataset. |
Hereditary spastic paralysis, infantile onset ascending Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset. |
Folate Malabsorption, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Folate Malabsorption, Hereditary from the curated CTD Gene-Disease Associations dataset. |
HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset. |
Bullous Dystrophy, Hereditary Macular Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bullous Dystrophy, Hereditary Macular Type from the curated CTD Gene-Disease Associations dataset. |
Amyloidosis, Hereditary, Transthyretin-Related Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Amyloidosis, Hereditary, Transthyretin-Related from the curated CTD Gene-Disease Associations dataset. |
Neutrophilia, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutrophilia, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Polyostotic osteolytic dysplasia, hereditary expansile Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polyostotic osteolytic dysplasia, hereditary expansile from the curated CTD Gene-Disease Associations dataset. |
Ptosis, Hereditary Congenital 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ptosis, Hereditary Congenital 1 from the curated CTD Gene-Disease Associations dataset. |
Optic Atrophies, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophies, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Telangiectasia, Hereditary Hemorrhagic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Telangiectasia, Hereditary Hemorrhagic from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type V Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type V from the curated CTD Gene-Disease Associations dataset. |
Exostoses, Multiple Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Exostoses, Multiple Hereditary from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, X-Linked 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, X-Linked 2 from the curated CTD Gene-Disease Associations dataset. |
Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type IIB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type IIB from the curated CTD Gene-Disease Associations dataset. |
Hereditary Angioedema Type III Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Angioedema Type III from the curated CTD Gene-Disease Associations dataset. |
LYMPHEDEMA, HEREDITARY, IC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease LYMPHEDEMA, HEREDITARY, IC from the curated CTD Gene-Disease Associations dataset. |
Hereditary Autoinflammatory Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Autoinflammatory Diseases from the curated CTD Gene-Disease Associations dataset. |
Hereditary Breast and Ovarian Cancer Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Breast and Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset. |
Ptosis, Hereditary Congenital 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ptosis, Hereditary Congenital 2 from the curated CTD Gene-Disease Associations dataset. |
Lymphedema, Hereditary, II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lymphedema, Hereditary, II from the curated CTD Gene-Disease Associations dataset. |
Lymphedema, Hereditary, IB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lymphedema, Hereditary, IB from the curated CTD Gene-Disease Associations dataset. |
Hereditary Myopathy with Early Respiratory Failure Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Myopathy with Early Respiratory Failure from the curated CTD Gene-Disease Associations dataset. |
Colorectal Cancer, Hereditary Nonpolyposis, Type 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Colorectal Cancer, Hereditary Nonpolyposis, Type 8 from the curated CTD Gene-Disease Associations dataset. |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 5 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 4 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 7 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 6 from the curated CTD Gene-Disease Associations dataset. |
Prostate Cancer, Hereditary, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Prostate Cancer, Hereditary, 3 from the curated CTD Gene-Disease Associations dataset. |
Coproporphyria, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Coproporphyria, Hereditary from the curated CTD Gene-Disease Associations dataset. |
PROSTATE CANCER, HEREDITARY, X-LINKED 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PROSTATE CANCER, HEREDITARY, X-LINKED 1 from the curated CTD Gene-Disease Associations dataset. |
Spherocytosis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spherocytosis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia from the curated CTD Gene-Disease Associations dataset. |
Keratitis, hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Keratitis, hereditary from the curated CTD Gene-Disease Associations dataset. |
Myopathy with Lactic Acidosis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy with Lactic Acidosis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Colorectal Neoplasms, Hereditary Nonpolyposis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Colorectal Neoplasms, Hereditary Nonpolyposis from the curated CTD Gene-Disease Associations dataset. |
Leukokeratosis, Hereditary Mucosal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leukokeratosis, Hereditary Mucosal from the curated CTD Gene-Disease Associations dataset. |
Spastic Paraplegia, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type Viib Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type Viib from the curated CTD Gene-Disease Associations dataset. |
Hereditary pancreatitis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary pancreatitis from the curated CTD Gene-Disease Associations dataset. |
Albright's hereditary osteodystrophy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Albright's hereditary osteodystrophy from the curated CTD Gene-Disease Associations dataset. |
Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, and Perinatal Edema from the curated CTD Gene-Disease Associations dataset. |
Adrenocortical Carcinoma, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Adrenocortical Carcinoma, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Hereditary macular coloboma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary macular coloboma from the curated CTD Gene-Disease Associations dataset. |
Hereditary Angioedema Types I and II Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Angioedema Types I and II from the curated CTD Gene-Disease Associations dataset. |
Desmoid disease, hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Desmoid disease, hereditary from the curated CTD Gene-Disease Associations dataset. |
Telangiectasia, Hereditary Hemorrhagic, Type 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Telangiectasia, Hereditary Hemorrhagic, Type 4 from the curated CTD Gene-Disease Associations dataset. |
Nephritis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Nephritis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Hereditary Sensory and Autonomic Neuropathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hereditary Sensory and Autonomic Neuropathies from the curated CTD Gene-Disease Associations dataset. |
Pyropoikilocytosis, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pyropoikilocytosis, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophies, Hereditary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophies, Hereditary from the curated CTD Gene-Disease Associations dataset. |
Telangiectasia, Hereditary Benign Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Telangiectasia, Hereditary Benign from the curated CTD Gene-Disease Associations dataset. |
hereditary spherocytosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary spherocytosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary hemorrhagic telangiectasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary hemorrhagic telangiectasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary spastic paraplegia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary spastic paraplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary elliptocytosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary elliptocytosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary angioedema Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary angioedema from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary fructose intolerance syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary fructose intolerance syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary lymphedema Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary lymphedema from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary mucosal leukokeratosis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary mucosal leukokeratosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary multiple exostoses Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hereditary multiple exostoses from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hereditary renal cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary lymphedema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary lymphedema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary multiple exostoses Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary multiple exostoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary hemorrhagic telangiectasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary hemorrhagic telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary spastic paraplegia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary spastic paraplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
albright's hereditary osteodystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease albright's hereditary osteodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary retinal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary retinal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary elliptocytosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary elliptocytosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary angioedema Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary angioedema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary night blindness Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary night blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
central nervous system hereditary degenerative disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease central nervous system hereditary degenerative disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary wilms' tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary wilms' tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary conventional renal cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary conventional renal cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary spherocytosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary spherocytosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary mucosal leukokeratosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary mucosal leukokeratosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary choroidal atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary fructose intolerance syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary fructose intolerance syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary breast ovarian cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary breast ovarian cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary coproporphyria Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary coproporphyria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary medullary thyroid carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary medullary thyroid carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary fructose intolerance. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary fructose intolerance. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary nonspherocytic hemolytic anemia (hnsha). Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary nonspherocytic hemolytic anemia (hnsha). in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene SetFrom GAD Gene-Disease Associations genes associated with the disease macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplastic syndromes, hereditary; pancreatic neoplasm; pancreatic neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplastic syndromes, hereditary; pancreatic neoplasm; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
eye diseases, hereditary; macular degeneration; retinal degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colonic neoplasms; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colonic neoplasms; colorectal neoplasms, hereditary nonpolyposis; microsatellite instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; endometrial neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; microsatellite instability; rectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; microsatellite instability; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
corneal dystrophies, hereditary; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease corneal dystrophies, hereditary; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anticipation, genetic; colorectal neoplasms, hereditary nonpolyposis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anticipation, genetic; colorectal neoplasms, hereditary nonpolyposis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diseases; hereditary central nervous system demyelinating diseases; leukoencephalopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hereditary and sporadic prostate cancer risk. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary and sporadic prostate cancer risk. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hemorrhagic telangiectasia, hereditary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hemorrhagic telangiectasia, hereditary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |