Progressive retinal degeneration

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Results for "Progressive retinal degeneration": 1001 gene sets

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progressive retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the progressive retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set From 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.
eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set From 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.
frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive cone degeneration Gene Set From HPO Gene-Disease Associations genes associated with the progressive cone degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Progressive rod-cone degeneration protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Progressive rod-cone degeneration protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Progressive Cerebellar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Skeletal dysplasia and progressive central nervous system degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal dysplasia and progressive central nervous system degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Generalized Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive retinal dystrophy due to retinol transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive retinal dystrophy due to retinol transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal degeneration, autosomal recessive, clumped pigment type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Late-Onset Retinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Late-Onset Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.
retinal degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease retinal degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
peripheral retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
blind vision; blindness; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blindness; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal degeneration; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal degeneration; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
color vision defects; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diseases in twins; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease diseases in twins; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; retinal drusen; wet macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; retinal drusen; wet macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal degeneration Gene Set From GWASdb SNP-Disease Associations genes associated with the disease retinal degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pigmentary retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the pigmentary retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
honeycomb retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the honeycomb retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystic retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cystic retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal degeneration protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal degeneration protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
retinal degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal outer nuclear layer degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal outer nuclear layer degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal rod cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal rod cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal cone cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal cone cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal ganglion cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal ganglion cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal photoreceptor degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal photoreceptor degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal degeneration, late-onset, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the retinal degeneration, late-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
infantile cerebellar-retinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal degeneration, autosomal recessive, clumped pigment type Gene Set From OMIM Gene-Disease Associations genes associated with the retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated OMIM Gene-Disease Associations dataset.
Infantile Cerebellar-Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cerebellar-Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Retinal Degeneration (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Retinal Degeneration (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystoid Macular Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystoid Macular Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glaucomatous Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glaucomatous Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Lattice Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Lattice Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Pigmentary Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigmentary Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Cystoid Retinal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Cystoid Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Retinal degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Retinal degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal lattice degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal lattice degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peripheral retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
late-onset retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease late-onset retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile cerebellar-retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cobblestone retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cobblestone retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Late-onset retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Late-onset retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebellar-retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lattice retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lattice retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
activated protein c resistance; retinal neovascularization; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; retinal neovascularization; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; retinal artery occlusion; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal artery occlusion; retinal vein occlusion Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal artery occlusion; retinal vein occlusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
Retinal detachment or retinal break Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment or retinal break phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal detachment with retinal break Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Retinal detachment with retinal break phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epilepsy, progressive myoclonic 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaze palsy, familial horizontal, with progressive scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy, progressive, with ovarian failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy, progressive, with ovarian failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive pseudorheumatoid dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive pseudorheumatoid dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperpigmentation, familial progressive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 2b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive myoclonus epilepsy with ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive myoclonus epilepsy with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive sclerosing poliodystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis with progressive nerve deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis with progressive nerve deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive myositis ossificans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive myositis ossificans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic Epilepsies, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myoclonic Epilepsies, Progressive from the curated CTD Gene-Disease Associations dataset.
Cataract, Nuclear Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Nuclear Progressive from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 from the curated CTD Gene-Disease Associations dataset.
Gliosis, Familial Progressive Subcortical Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.
Osseous Heteroplasia, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osseous Heteroplasia, Progressive from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Supranuclear Palsy, Progressive, 2 from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Supranuclear Palsy, Progressive, 3 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Progressive Myoclonic, 1b Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Progressive Myoclonic, 1b from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.
Chorioretinal atrophy, progressive bifocal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset.
Macrothrombocytopenia progressive deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrothrombocytopenia progressive deafness from the curated CTD Gene-Disease Associations dataset.
Erythrokeratodermia, Progressive Symmetric Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrokeratodermia, Progressive Symmetric from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness from the curated CTD Gene-Disease Associations dataset.
Progressive hearing loss stapes fixation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive hearing loss stapes fixation from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Supranuclear Palsy, Progressive from the curated CTD Gene-Disease Associations dataset.
Arthropathy, progressive pseudorheumatoid, of childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthropathy, progressive pseudorheumatoid, of childhood from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy, Progressive Multifocal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy, Progressive Multifocal from the curated CTD Gene-Disease Associations dataset.
Progressive Familial Heart Block, Type Ib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.
Bulbar Palsy, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bulbar Palsy, Progressive from the curated CTD Gene-Disease Associations dataset.
Ophthalmoplegia, Chronic Progressive External Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ophthalmoplegia, Chronic Progressive External from the curated CTD Gene-Disease Associations dataset.
Nephropathy, Progressive, with Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephropathy, Progressive, with Deafness from the curated CTD Gene-Disease Associations dataset.
Progressive supranuclear palsy atypical Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive supranuclear palsy atypical from the curated CTD Gene-Disease Associations dataset.
Renal Failure, Progressive, with Hypertension Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Failure, Progressive, with Hypertension from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Supranuclear Palsy, Progressive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
chronic progressive external ophthalmoplegia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease chronic progressive external ophthalmoplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
progressive myoclonus epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease progressive myoclonus epilepsy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
progressive supranuclear palsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease progressive supranuclear palsy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
progressive supranuclear palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive supranuclear palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive bulbar palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive bulbar palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic progressive external ophthalmoplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic progressive external ophthalmoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive multifocal leukoencephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive multifocal leukoencephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
rapidly progressive glomerulonephritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease rapidly progressive glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive myoclonus epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive myoclonus epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
slowly progressive als Gene Set From GAD Gene-Disease Associations genes associated with the disease slowly progressive als in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial atypical progressive supranuclear palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia, primary progressive; dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia, primary progressive; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ophthalmoplegia, chronic progressive external Gene Set From GAD Gene-Disease Associations genes associated with the disease ophthalmoplegia, chronic progressive external in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
primary progressive aphasia Gene Set From GAD Gene-Disease Associations genes associated with the disease primary progressive aphasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive supranuclear palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neurodegenerative diseases; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dominant progressive deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease dominant progressive deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia, primary progressive; heredodegenerative disorders, nervous system Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia, primary progressive; heredodegenerative disorders, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rapidly progressive familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease rapidly progressive familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain diseases; neurodegenerative diseases; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease brain diseases; neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive av-block and anomalous venous return Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive av-block and anomalous venous return in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive external ophthalmoplegia Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive external ophthalmoplegia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; huntington disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive renal damage Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive renal damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; huntington disease; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; huntington disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term progressive in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
progressive supranuclear palsy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease progressive supranuclear palsy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
progressive cataract Gene Set From HPO Gene-Disease Associations genes associated with the progressive cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive inability to walk Gene Set From HPO Gene-Disease Associations genes associated with the progressive inability to walk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive congenital scoliosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive congenital scoliosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive visual field defects Gene Set From HPO Gene-Disease Associations genes associated with the progressive visual field defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symmetrical progressive peripheral demyelination Gene Set From HPO Gene-Disease Associations genes associated with the symmetrical progressive peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive spastic paraplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive spastic paraplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive vitiligo Gene Set From HPO Gene-Disease Associations genes associated with the progressive vitiligo phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive neurologic deterioration Gene Set From HPO Gene-Disease Associations genes associated with the progressive neurologic deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive spastic quadriplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive spastic quadriplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive psychomotor deterioration Gene Set From HPO Gene-Disease Associations genes associated with the progressive psychomotor deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive reticulate hyperpigmentation Gene Set From HPO Gene-Disease Associations genes associated with the progressive reticulate hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive fusion 2nd-5th pip joints Gene Set From HPO Gene-Disease Associations genes associated with the progressive fusion 2nd-5th pip joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive extrapyramidal movement disorder Gene Set From HPO Gene-Disease Associations genes associated with the progressive extrapyramidal movement disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive gait ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive gait ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive inspiratory stridor Gene Set From HPO Gene-Disease Associations genes associated with the progressive inspiratory stridor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive choreoathetosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive choreoathetosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive spasticity Gene Set From HPO Gene-Disease Associations genes associated with the progressive spasticity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive peripheral neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive sclerosis of skull base Gene Set From HPO Gene-Disease Associations genes associated with the progressive sclerosis of skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive clavicular acroosteolysis Gene Set From HPO Gene-Disease Associations genes associated with the progressive clavicular acroosteolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive alopecia Gene Set From HPO Gene-Disease Associations genes associated with the progressive alopecia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive truncal ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive truncal ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subacute progressive viral hepatitis Gene Set From HPO Gene-Disease Associations genes associated with the subacute progressive viral hepatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intellectual disability, progressive Gene Set From HPO Gene-Disease Associations genes associated with the intellectual disability, progressive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive central visual loss Gene Set From HPO Gene-Disease Associations genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive language deterioration Gene Set From HPO Gene-Disease Associations genes associated with the progressive language deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive hyperpigmentation Gene Set From HPO Gene-Disease Associations genes associated with the progressive hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive hypotrichosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive hypotrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive pulmonary function impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive pulmonary function impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive forgetfulness Gene Set From HPO Gene-Disease Associations genes associated with the progressive forgetfulness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive microcephaly Gene Set From HPO Gene-Disease Associations genes associated with the progressive microcephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive alveolar ridge hypertropy Gene Set From HPO Gene-Disease Associations genes associated with the progressive alveolar ridge hypertropy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive proximal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive macrocephaly Gene Set From HPO Gene-Disease Associations genes associated with the progressive macrocephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive external ophthalmoplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive external ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive night blindness Gene Set From HPO Gene-Disease Associations genes associated with the progressive night blindness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive macular scarring Gene Set From HPO Gene-Disease Associations genes associated with the progressive macular scarring phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive ptosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive ptosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive calcification of costochondral cartilage Gene Set From HPO Gene-Disease Associations genes associated with the progressive calcification of costochondral cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cervical vertebral spine fusion Gene Set From HPO Gene-Disease Associations genes associated with the progressive cervical vertebral spine fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive conductive hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive conductive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rapidly progressive Gene Set From HPO Gene-Disease Associations genes associated with the rapidly progressive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive leukoencephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive leukoencephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive flexion contractures Gene Set From HPO Gene-Disease Associations genes associated with the progressive flexion contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive visual loss Gene Set From HPO Gene-Disease Associations genes associated with the progressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive disorder Gene Set From HPO Gene-Disease Associations genes associated with the progressive disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive ophthalmoplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cerebellar ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive cerebellar ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Multiple Sclerosis, Chronic Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis, Chronic Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myoclonic Epilepsies, Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myoclonic Epilepsies, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Bulbar Palsy, Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Bulbar Palsy, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Supranuclear Palsy, Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Supranuclear Palsy, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Aphasia, Primary Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aphasia, Primary Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ophthalmoplegia, Chronic Progressive External Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ophthalmoplegia, Chronic Progressive External phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Progressive ankylosis Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Progressive ankylosis protein domain from the InterPro Predicted Protein Domain Annotations dataset.
progressive muscle weakness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
progressive hair loss Gene Set From MPO Gene-Phenotype Associations gene mutations causing the progressive hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
deafness, x-linked 1, progressive Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, x-linked 1, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive canalicular Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive canalicular phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 2b (lafora) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 2b (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal dominant, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal dominant, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive familial heart block, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
macrothrombocytopenia and progressive sensorineural deafness Gene Set From OMIM Gene-Disease Associations genes associated with the macrothrombocytopenia and progressive sensorineural deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive atypical Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive atypical phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperpigmentation, familial progressive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperpigmentation, familial progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
aphasia, primary progressive Gene Set From OMIM Gene-Disease Associations genes associated with the aphasia, primary progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepiphyseal dysplasia tarda with progressive arthropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepiphyseal dysplasia tarda with progressive arthropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene Set From OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy, progressive x-linked, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy, progressive, with ovarian failure Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy, progressive, with ovarian failure phenotype from the curated OMIM Gene-Disease Associations dataset.
osseous heteroplasia, progressive Gene Set From OMIM Gene-Disease Associations genes associated with the osseous heteroplasia, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.
nephropathy, progressive, with deafness Gene Set From OMIM Gene-Disease Associations genes associated with the nephropathy, progressive, with deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
gaze palsy, horizontal, with progressive scoliosis Gene Set From OMIM Gene-Disease Associations genes associated with the gaze palsy, horizontal, with progressive scoliosis phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
arthropathy, progressive pseudorheumatoid, of childhood Gene Set From OMIM Gene-Disease Associations genes associated with the arthropathy, progressive pseudorheumatoid, of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions 3 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, progressive, with or without lipodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 27, nuclear progressive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 27, nuclear progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
heart block, progressive, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the heart block, progressive, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 1a (unverricht and lundborg) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 1a (unverricht and lundborg) phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 1b Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 2a (lafora) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 2a (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.
Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 Gene Set From Reactome Pathways 2014 proteins participating in the Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 pathway from the Reactome Pathways dataset.
Primary Progressive Aphasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Progressive Aphasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone Dystrophy (Without Rod Involvement) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy (Without Rod Involvement) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cgvhd Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cgvhd in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Intrahepatic Cholestasis (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Intrahepatic Cholestasis (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Rapidly Progressive Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Rapidly Progressive Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Slowly Progressive Insulin Dependent Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Slowly Progressive Insulin Dependent Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Supranuclear Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Supranuclear Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Pseudorheumatoid Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Pseudorheumatoid Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Primary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Primary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Progressive External Ophthalmoplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Progressive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Progressive Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone-Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone-Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe Intellectual Disability And Progressive Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Intellectual Disability And Progressive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Progressive Nonfluent Aphasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Progressive Nonfluent Aphasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Distal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Post Hemorrhagic Ventricular Dilatation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Post Hemorrhagic Ventricular Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Dementia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Dementia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Progressive Chorea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Progressive Chorea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Bulbar Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Bulbar Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalopathy With Edema, Hypsarrhythmia, And Optic Atrophy-Like Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Secondary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Secondary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Chronic Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Chronic Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Periodontitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Ptosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Ptosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Brain Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Brain Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Ophthalmoplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cardiomyopathic Lentiginosis Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cardiomyopathic Lentiginosis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Non-Small Cell Lung Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Non-Small Cell Lung Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ophthalmoplegia, Progressive Supranuclear Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ophthalmoplegia, Progressive Supranuclear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Supranuclear Palsy, Progressive, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Atrophy, Progressive Bifocal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy, Progressive Bifocal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Failure, Progressive, With Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Failure, Progressive, With Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pf-Ild-Progressive Fibrosing Interstitial Lung Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pf-Ild-Progressive Fibrosing Interstitial Lung Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Logopenic Progressive Aphasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Logopenic Progressive Aphasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalomyelitis With Rigidity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalomyelitis With Rigidity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symmetrical Progressive Peripheral Demyelination Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symmetrical Progressive Peripheral Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Hearing Loss Stapes Fixation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Hearing Loss Stapes Fixation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Chorea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Chorea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Non-Progressive Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Non-Progressive Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prickle1-Related Progressive Myoclonus Epilepsy With Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prickle1-Related Progressive Myoclonus Epilepsy With Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Piebaldism, Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Piebaldism, Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Progressive Hyper And Hypopigmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Hyper And Hypopigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Reticulate Hyperpigmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Reticulate Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Subcortical Gliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Subcortical Gliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 1, Atypical Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Supranuclear Palsy, Progressive, 1, Atypical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Impairment And Progressive Phthisis Bulbi Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Impairment And Progressive Phthisis Bulbi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macrothrombocytopenia And Progressive Sensorineural Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macrothrombocytopenia And Progressive Sensorineural Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cavitating Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cavitating Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysphagia, Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysphagia, Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Congenital Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Congenital Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Polyneuropathy With Bilateral Striatal Necrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Polyneuropathy With Bilateral Striatal Necrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Progressive Bulbar Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Progressive Bulbar Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Proximal Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Proximal Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Myoclonic Epilepsy With Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Myoclonic Epilepsy With Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Familial Heart Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Familial Heart Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Leukoencephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Peripheral Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Night Blindness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Night Blindness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Neoplastic Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Neoplastic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Neurologic Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Neurologic Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Paraplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spasticity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Proximal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Microcephaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intellectual Disability, Progressive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intellectual Disability, Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Quadriplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Cervical Vertebral Spine Fusion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Cervical Vertebral Spine Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Paraparesis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Paraparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Flexion Contractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Flexion Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Macrocephaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Macrocephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Gait Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Gait Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Inability To Walk Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Inability To Walk in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Pes Cavus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Pes Cavus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Subacute Progressive Viral Hepatitis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subacute Progressive Viral Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Rapidly Progressive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rapidly Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Psychomotor Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Psychomotor Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Paraparesis, Chronic Progressive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paraparesis, Chronic Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Extrapyramidal Movement Disorder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Extrapyramidal Movement Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Intervertebral Space Narrowing Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Intervertebral Space Narrowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Clavicular Acroosteolysis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Clavicular Acroosteolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Conductive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Conductive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Visual Field Defects Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Field Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Distal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sensorineural Hearing Loss, Progressive Bilateral Postlingual Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sensorineural Hearing Loss, Progressive Bilateral Postlingual in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Ventriculomegaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Language Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Language Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Calcification Of Costochondral Cartilage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Calcification Of Costochondral Cartilage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Alveolar Ridge Hypertropy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Alveolar Ridge Hypertropy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Forgetfulness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Forgetfulness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Truncal Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Truncal Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Hyperpigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Choreoathetosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Choreoathetosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Loss Of Facial Adipose Tissue Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Loss Of Facial Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Extrapyramidal Muscular Rigidity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Extrapyramidal Muscular Rigidity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Leg Bowing Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Leg Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Vitiligo Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Vitiligo in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Hypotrichosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Hypotrichosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Pulmonary Function Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Pulmonary Function Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Fusion 2Nd-5Th Pip Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Fusion 2Nd-5Th Pip Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Sclerosis Of Skull Base Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Sclerosis Of Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Inspiratory Stridor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Inspiratory Stridor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Alopecia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
progressive muscle weakness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased sperm progressive motility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased sperm progressive motility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
progressive hair loss Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sperm progressive motility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sperm progressive motility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 Gene Set From Reactome Pathways 2024 proteins participating in the Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 pathway from the Reactome Pathways 2024 dataset.
Chronic progressive external ophthalmoplegia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chronic progressive external ophthalmoplegia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive familial heart block Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive familial heart block from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive bulbar palsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive bulbar palsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive familial intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive supranuclear palsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive supranuclear palsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1B Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 1B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with progressive myoclonic epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive osseous heteroplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive osseous heteroplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 4 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 4 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive pseudorheumatoid arthropathy of childhood Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive pseudorheumatoid arthropathy of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive bulbar palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive bulbar palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive supranuclear palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive supranuclear palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary progressive multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary progressive multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic progressive external ophthalmoplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic progressive external ophthalmoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary progressive aphasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary progressive aphasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic tetraplegia, thin corpus callosum, and progressive microcephaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic tetraplegia, thin corpus callosum, and progressive microcephaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive non-fluent aphasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive non-fluent aphasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive leukoencephalopathy with ovarian failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive leukoencephalopathy with ovarian failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive multifocal leukoencephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive multifocal leukoencephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rapidly progressive glomerulonephritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rapidly progressive glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive relapsing multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive relapsing multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with progressive myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Logopenic progressive aphasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Logopenic progressive aphasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type IA Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type IA in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive osseous heteroplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive osseous heteroplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type II Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type IB Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type IB in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial progressive hyperpigmentation with or without hypopigmentation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial progressive hyperpigmentation with or without hypopigmentation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early onset progressive encephalopathy with brain atrophy and thin corpus callosum Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset progressive encephalopathy with brain atrophy and thin corpus callosum in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive pseudorheumatoid arthropathy of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive pseudorheumatoid arthropathy of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic progressive polyneuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic progressive polyneuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual impairment and progressive phthisis bulbi in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive myoclonic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive distal muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive proximal muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sclerosing poliodystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive pseudorheumatoid dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive pseudorheumatoid dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive familial intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive cone dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive cone dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive familial heart block Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive familial heart block phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive supranuclear palsy-parkinsonism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive supranuclear palsy-parkinsonism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive supranuclear ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive supranuclear ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive osseous heteroplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive osseous heteroplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive scapulohumeroperoneal distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive scapulohumeroperoneal distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive myositis ossificans Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive myositis ossificans phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy-progressive myoclonic epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual disability-progressive spastic diplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-progressive spastic diplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked progressive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked progressive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic and progressive ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chronic and progressive ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-progressive congenital cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-progressive congenital cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary progressive aphasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary progressive aphasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive demyelinating neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive demyelinating neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive neurologic deterioration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive neurologic deterioration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive bulbar palsy of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive bulbar palsy of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary progressive multiple sclerosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary progressive multiple sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive spasticity Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive spasticity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive childhood encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive childhood encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive microcephaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive gait ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive gait ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual impairment and progressive phthisis bulbi phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Macular degeneration, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular degeneration, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pigmentary pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pigmentary pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia, high, with cataract and vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular Degeneration, Age-Related, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 11 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 10 from the curated CTD Gene-Disease Associations dataset.
Snowflake vitreoretinal degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Snowflake vitreoretinal degeneration from the curated CTD Gene-Disease Associations dataset.
CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 9 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 3 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 2 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 1 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 7 from the curated CTD Gene-Disease Associations dataset.
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED from the curated CTD Gene-Disease Associations dataset.
Intervertebral Disc Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intervertebral Disc Degeneration from the curated CTD Gene-Disease Associations dataset.
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset.
Nerve Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nerve Degeneration from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 4 from the curated CTD Gene-Disease Associations dataset.
Striatonigral degeneration infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Striatonigral degeneration infantile from the curated CTD Gene-Disease Associations dataset.
Striatal Degeneration, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Striatal Degeneration, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Hyaloideoretinal degeneration of Wagner Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyaloideoretinal degeneration of Wagner from the curated CTD Gene-Disease Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile macular degeneration and hypotrichosis from the curated CTD Gene-Disease Associations dataset.
Wallerian Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wallerian Degeneration from the curated CTD Gene-Disease Associations dataset.
Frontotemporal Lobar Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Frontotemporal Lobar Degeneration from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Hepatolenticular Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatolenticular Degeneration from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Macular Degeneration in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease macular degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
spinocerebellar degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinocerebellar degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cerebral degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cerebral degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
age related macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease age related macular degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
degeneration of macula and posterior pole Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease degeneration of macula and posterior pole from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
macular degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease macular degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
striatonigral degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease striatonigral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinocerebellar degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinocerebellar degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
kuhnt-junius degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease kuhnt-junius degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
corneal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
age related macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease age related macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
conjunctival degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease conjunctival degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
degeneration of macula and posterior pole Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease degeneration of macula and posterior pole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
primary cerebellar degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary cerebellar degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cardiovascular diseases; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; geographic atrophy; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroiditis; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroiditis; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chlamydia infections; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease chlamydia infections; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; stargardt disease Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; stargardt disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatolenticular degeneration; movement disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatolenticular degeneration; movement disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-related macular degeneration (wet) Gene Set From GAD Gene-Disease Associations genes associated with the disease age-related macular degeneration (wet) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
wet macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease wet macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal dominant macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal dominant macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cone degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cone degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mitochondrial diseases; nerve degeneration; presbycusis Gene Set From GAD Gene-Disease Associations genes associated with the disease mitochondrial diseases; nerve degeneration; presbycusis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intervertebral disk degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease intervertebral disk degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration, age-related Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration, age-related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial age-related macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatolenticular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatolenticular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain injuries; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease brain injuries; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; neovascularization, pathologic Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; neovascularization, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intervertebral disk degeneration; intervertebral disk displacement Gene Set From GAD Gene-Disease Associations genes associated with the disease intervertebral disk degeneration; intervertebral disk displacement in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angiomatosis; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease angiomatosis; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; vision, low Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; soft drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; soft drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; hypertension; macular degeneration; prostatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hypertension; macular degeneration; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; inflammation; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; inflammation; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatolenticular degeneration; liver failure, acute Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatolenticular degeneration; liver failure, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disc degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease disc degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; cholesterol, hdl; triglycerides; atherosclerosis, coronary; macular degeneration; colorectal cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; cholesterol, hdl; triglycerides; atherosclerosis, coronary; macular degeneration; colorectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dna damage; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease dna damage; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
occupational exposure in lumbar disc degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease occupational exposure in lumbar disc degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disc degeneration, lumbar spine Gene Set From GAD Gene-Disease Associations genes associated with the disease disc degeneration, lumbar spine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-related macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal disc degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal disc degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; inflammation; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; inflammation; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nerve degeneration; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease nerve degeneration; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
degeneration of intervertebral discs Gene Set From GAD Gene-Disease Associations genes associated with the disease degeneration of intervertebral discs in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chlamydophila infections; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease chlamydophila infections; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ache, low back; intervertebral disk degeneration; low back pain Gene Set From GAD Gene-Disease Associations genes associated with the disease ache, low back; intervertebral disk degeneration; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; inflammatory bowel diseases; macular degeneration; prostatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; inflammatory bowel diseases; macular degeneration; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; cardiovascular diseases; colorectal neoplasms; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; cardiovascular diseases; colorectal neoplasms; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal lobar degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal lobar degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
degeneration Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term degeneration in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Age-related macular degeneration (CNV vs. GA) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (CNV vs. GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (GA) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (CNV) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (CNV) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (wet) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (wet) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (extreme sampling) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (extreme sampling) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Disc degeneration (lumbar) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Disc degeneration (lumbar) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
macular degeneration Gene Set From GWASdb SNP-Disease Associations genes associated with the disease macular degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
age related macular degeneration Gene Set From GWASdb SNP-Disease Associations genes associated with the disease age related macular degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
degeneration of macula and posterior pole Gene Set From GWASdb SNP-Disease Associations genes associated with the disease degeneration of macula and posterior pole in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
age-related macular degeneration Gene Set From GWASdb SNP-Phenotype Associations genes associated with the age-related macular degeneration phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
macular degeneration Gene Set From GWASdb SNP-Phenotype Associations genes associated with the macular degeneration phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
intervertebral disc degeneration Gene Set From GWASdb SNP-Phenotype Associations genes associated with the intervertebral disc degeneration phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
atrophy/degeneration affecting the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
atrophy/degeneration affecting the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dorsal column degeneration Gene Set From HPO Gene-Disease Associations genes associated with the dorsal column degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the corticospinal tracts Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
choroidoretinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the choroidoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral vitreoretinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the peripheral vitreoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pallidal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the pallidal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tapetoretinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the tapetoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystoid macular degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cystoid macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinocerebellar tract degeneration Gene Set From HPO Gene-Disease Associations genes associated with the spinocerebellar tract degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular degeneration Gene Set From HPO Gene-Disease Associations genes associated with the macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cerebral degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
axonal degeneration/regeneration Gene Set From HPO Gene-Disease Associations genes associated with the axonal degeneration/regeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cochlear degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cochlear degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
late-onset spinocerebellar degeneration Gene Set From HPO Gene-Disease Associations genes associated with the late-onset spinocerebellar degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the cerebrum Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the brainstem Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the caudate nucleus Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the caudate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vitreoretinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the vitreoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral axonal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the peripheral axonal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
age-related macular degeneration Gene Set From HPO Gene-Disease Associations genes associated with the age-related macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
choroidal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the choroidal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
granulovacuolar degeneration Gene Set From HPO Gene-Disease Associations genes associated with the granulovacuolar degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
corneal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the corneal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
degeneration of the lateral corticospinal tracts Gene Set From HPO Gene-Disease Associations genes associated with the degeneration of the lateral corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
central nervous system degeneration Gene Set From HPO Gene-Disease Associations genes associated with the central nervous system degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intervertebral disc degeneration Gene Set From HPO Gene-Disease Associations genes associated with the intervertebral disc degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
degeneration of anterior horn cells Gene Set From HPO Gene-Disease Associations genes associated with the degeneration of anterior horn cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Macular Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Macular Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Wet Macular Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Wet Macular Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Frontotemporal Lobar Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Frontotemporal Lobar Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Nerve Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Nerve Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Intervertebral Disk Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Intervertebral Disk Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hepatolenticular Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hepatolenticular Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebellar degeneration-related protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cerebellar degeneration-related protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
vestibular hair cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neural tube degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the neural tube degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
stria vascularis degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the stria vascularis degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
epididymis epithelium degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the epididymis epithelium degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear inner hair cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear inner hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear hair cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
inner cell mass degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the inner cell mass degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spiral ligament degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spiral ligament degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
amacrine cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the amacrine cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscle degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the muscle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
wolffian duct degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the wolffian duct degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
liver degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the liver degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
myocardial fiber degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the myocardial fiber degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
embryonic epiblast cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the embryonic epiblast cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neuron degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the neuron degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
intervertebral disk degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intervertebral disk degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mullerian duct degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the mullerian duct degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
purkinje cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the purkinje cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cervical vertebrae degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cervical vertebrae degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
oocyte degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the oocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hair follicle degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hair follicle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
photoreceptor inner segment degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the photoreceptor inner segment degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
heart right ventricle degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the heart right ventricle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ovary degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ovary degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal wallerian degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal wallerian degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pillar cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pillar cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vestibular saccular degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular saccular degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
type ii spiral ligament fibrocyte degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the type ii spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vestibular ganglion degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular ganglion degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
photoreceptor outer segment degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the photoreceptor outer segment degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vestibular dark cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular dark cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebral cortex pyramidal cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cerebral cortex pyramidal cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dorsal root ganglion degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dorsal root ganglion degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hippocampal neuron degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hippocampal neuron degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
degeneration of organ of corti supporting cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the degeneration of organ of corti supporting cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
axon degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the axon degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
type i spiral ligament fibrocyte degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the type i spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cardiac muscle degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cardiac muscle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
utricular macular degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the utricular macular degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vestibular saccular macula degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular saccular macula degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
utricular degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the utricular degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
notochord degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the notochord degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
type iv spiral ligament fibrocyte degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the type iv spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hippocampus pyramidal cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hippocampus pyramidal cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
motor neuron degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the motor neuron degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle fiber degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fiber degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear ganglion degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear ganglion degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
peripheral nervous system degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the peripheral nervous system degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spinal cord degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spinal cord degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
seminiferous tubule degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the seminiferous tubule degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
trophectoderm cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the trophectoderm cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear outer hair cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear outer hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ameloblast degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ameloblast degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
superior cervical ganglion degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the superior cervical ganglion degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
deiters cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the deiters cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
slow wallerian degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the slow wallerian degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
organ of corti degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the organ of corti degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
type iii spiral ligament fibrocyte degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the type iii spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
epididymis degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the epididymis degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mental retardation, severe, with spasticity and tapetoretinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, severe, with spasticity and tapetoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
striatal degeneration, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the striatal degeneration, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
{lumbar disc degeneration} Gene Set From OMIM Gene-Disease Associations genes associated with the {lumbar disc degeneration} phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 15, suscepbitility to Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 15, suscepbitility to phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 14, reduced risk of} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 14, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopia, high, with cataract and vitreoretinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, neovascular type} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, neovascular type} phenotype from the curated OMIM Gene-Disease Associations dataset.
snowflake vitreoretinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the snowflake vitreoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
frontotemporal lobar degeneration, tardbp-related Gene Set From OMIM Gene-Disease Associations genes associated with the frontotemporal lobar degeneration, tardbp-related phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, susceptibility to 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, susceptibility to 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 10} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, reduced risk of} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.
{?macular degeneration, age-related} Gene Set From OMIM Gene-Disease Associations genes associated with the {?macular degeneration, age-related} phenotype from the curated OMIM Gene-Disease Associations dataset.
doyne honeycomb degeneration of retina Gene Set From OMIM Gene-Disease Associations genes associated with the doyne honeycomb degeneration of retina phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, juvenile Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, x-linked atrophic Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, x-linked atrophic phenotype from the curated OMIM Gene-Disease Associations dataset.
frontotemporal lobar degeneration with ubiquitin-positive inclusions Gene Set From OMIM Gene-Disease Associations genes associated with the frontotemporal lobar degeneration with ubiquitin-positive inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 7} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 13, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 13, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 9} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.
striatonigral degeneration, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the striatonigral degeneration, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
Hepatolenticular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatolenticular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Age Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Age Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exudative Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exudative Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exudative Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exudative Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Photoreceptor Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Photoreceptor Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitreoretinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitreoretinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Degeneration Of Lumbar Intervertebral Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Degeneration Of Lumbar Intervertebral Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intervertebral Disc Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intervertebral Disc Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pallidopontonigral Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pallidopontonigral Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscle Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscle Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Wet Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Wet Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Degeneration Of The Striatum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Degeneration Of The Striatum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stiatonigral Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stiatonigral Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontotemporal Lobar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontotemporal Lobar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Meniscal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Meniscal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Cerebellar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Cerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corticobasal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corticobasal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinocerebellar Tract Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinocerebellar Tract Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vascular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vascular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatonigral Degeneration, Infantile, Mitochondrial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatonigral Degeneration, Infantile, Mitochondrial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy/Degeneration Affecting The Brainstem Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy/Degeneration Affecting The Brainstem in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nervous System--Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nervous System--Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pallidoluysian Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pallidoluysian Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Degeneration Of Spine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Degeneration Of Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facet Joint Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facet Joint Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Snowflake Vitreoretinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Snowflake Vitreoretinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Combined Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Combined Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonexudative Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonexudative Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyaloideoretinal Degeneration Of Wagner Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyaloideoretinal Degeneration Of Wagner in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitreous Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitreous Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corneal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corneal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatonigral Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatonigral Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Basal Ganglion Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Basal Ganglion Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Age-Related Macular Degeneration Type 11 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Age-Related Macular Degeneration Type 11 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Pigmentary Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Pigmentary Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Degeneration, Subacute Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Degeneration, Subacute in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Cerebellar Degeneration, Anti-Yo-Associated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Cerebellar Degeneration, Anti-Yo-Associated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myopic Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myopic Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mptp-Induced Degeneration Of The Striatum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mptp-Induced Degeneration Of The Striatum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cns Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cns Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arteriovascular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arteriovascular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pallidal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pallidal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatal Degeneration, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatal Degeneration, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypertrophic Olivary Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypertrophic Olivary Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corticostriatal-Spinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corticostriatal-Spinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lumbar Spine Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lumbar Spine Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Cord Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Cord Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurofibrillary Degeneration (Morphologic Abnormality) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurofibrillary Degeneration (Morphologic Abnormality) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nerve Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nerve Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Macular Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Nervous System Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Nervous System Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Caudate Nucleus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Caudate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pigmentary Iris Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pigmentary Iris Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axonal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Axonal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Axonal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Degeneration Of Anterior Horn Cells Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Degeneration Of Anterior Horn Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Degeneration Of The Lateral Corticospinal Tracts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Degeneration Of The Lateral Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dry Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dry Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dorsal Column Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dorsal Column Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Corticospinal Tracts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retrograde Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retrograde Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Wallerian Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wallerian Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cochlear Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cochlear Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Late-Onset Spinocerebellar Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Spinocerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axonal Degeneration/Regeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Degeneration/Regeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Granulovacuolar Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Granulovacuolar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Vitreoretinal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Vitreoretinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Spinal Cord Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Affecting The Central Nervous System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Affecting The Cerebrum Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Cerebrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
oocyte degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the oocyte degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
notochord degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the notochord degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
epididymis degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the epididymis degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cochlear ganglion degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear ganglion degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vestibular hair cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Purkinje cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Purkinje cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cochlear hair cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cochlear inner hair cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear inner hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cochlear outer hair cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear outer hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
organ of Corti degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the organ of Corti degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
degeneration of organ of Corti supporting cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the degeneration of organ of Corti supporting cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina photoreceptor degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina photoreceptor degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina outer nuclear layer degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina outer nuclear layer degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
photoreceptor outer segment degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the photoreceptor outer segment degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
seminiferous tubule degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the seminiferous tubule degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neuron degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neuron degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
slow Wallerian degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the slow Wallerian degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
muscle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the muscle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ameloblast degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ameloblast degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ovary degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vestibular ganglion degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular ganglion degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
motor neuron degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the motor neuron degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vestibular saccular macula degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular saccular macula degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pillar cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pillar cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hippocampal neuron degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hippocampal neuron degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina ganglion cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina ganglion cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
inner cell mass degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the inner cell mass degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
myocardial fiber degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the myocardial fiber degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Deiters cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Deiters cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
utricular macular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the utricular macular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
liver degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the liver degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vestibular dark cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular dark cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic nerve degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic nerve degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Wolffian duct degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Wolffian duct degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
axon degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the axon degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
amacrine cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the amacrine cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
stria vascularis degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the stria vascularis degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
epididymis epithelium degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the epididymis epithelium degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
testis degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the testis degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spiral ligament degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spiral ligament degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hair follicle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hair follicle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
superior cervical ganglion degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the superior cervical ganglion degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina cone cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina cone cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle fiber degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle fiber degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cardiac muscle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cardiac muscle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
facial muscle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the facial muscle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intervertebral disk degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intervertebral disk degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Mullerian duct degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Mullerian duct degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
peripheral nervous system degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the peripheral nervous system degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
type I spiral ligament fibrocyte degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the type I spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
type III spiral ligament fibrocyte degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the type III spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spinal cord degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spinal cord degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cochlear degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
type II spiral ligament fibrocyte degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the type II spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
type IV spiral ligament fibrocyte degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the type IV spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
trophectoderm cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the trophectoderm cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hippocampus pyramidal cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hippocampus pyramidal cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina rod cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina rod cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
heart right ventricle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the heart right ventricle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic epiblast cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic epiblast cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cervical vertebrae degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cervical vertebrae degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vestibular saccular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular saccular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
utricular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the utricular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neural tube degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neural tube degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
seminal vesicle epithelium degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the seminal vesicle epithelium degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
photoreceptor inner segment degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the photoreceptor inner segment degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal Wallerian degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Wallerian degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cerebral cortex pyramidal cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebral cortex pyramidal cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
gastric gland degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the gastric gland degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nasal gland degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nasal gland degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
salivary gland degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the salivary gland degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pancreas degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
dorsal root ganglion degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the dorsal root ganglion degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina macular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina macular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Meibomian gland degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Meibomian gland degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Degeneration of macula and posterior pole Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Degeneration of macula and posterior pole from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Age related macular degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Macular degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Age related macular degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Degeneration of macula and posterior pole Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Degeneration of macula and posterior pole in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Macular degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Kuhnt-Junius degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Kuhnt-Junius degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Degeneration of macula and posterior pole Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Degeneration of macula and posterior pole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Corneal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked atrophic macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked atrophic macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Kuhnt-Junius degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Kuhnt-Junius degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Striatonigral degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Striatonigral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary cerebellar degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary cerebellar degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Conjunctival degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Conjunctival degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Corticobasal degeneration syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corticobasal degeneration syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pulp degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulp degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Snowflake vitreoretinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Snowflake vitreoretinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Age related macular degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spongy degeneration of central nervous system Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spongy degeneration of central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pigmentary pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pigmentary pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macular degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macular degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Age-related macular degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Age-related macular degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Snowflake vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Snowflake vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Trichomegaly-retina pigmentary degeneration-dwarfism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GRN-related frontotemporal lobar degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GRN-related frontotemporal lobar degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Striatal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Striatal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Striatonigral degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Striatonigral degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Helicoid peripapillary chorioretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Helicoid peripapillary chorioretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrophy/Degeneration affecting the central nervous system Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrophy/Degeneration affecting the central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Corticobasal degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corticobasal degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Advanced age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Advanced age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exudative age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exudative age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (SNP x mitochondrial G12771A interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (SNP x mitochondrial G12771A interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disc degeneration (lumbar) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disc degeneration (lumbar) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to ranibizumab in age-related macular degeneration (exudative) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to ranibizumab in age-related macular degeneration (exudative) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (extreme sampling) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (extreme sampling) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (wet) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (wet) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (choroidal neovascularisation) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (choroidal neovascularisation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (geographic atrophy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (geographic atrophy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (CNV vs. GA) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (CNV vs. GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Laterality in neovascular age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Laterality in neovascular age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (MTAG) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neovascular age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neovascular age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression in age-related macular degeneration (adjusted for baseline) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression in age-related macular degeneration (adjusted for baseline) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression to geographic atrophy form in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression to geographic atrophy form in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression to choroidal neovascularization form in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression to choroidal neovascularization form in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to antioxidants and zinc in age-related macular degeneration (disease progression) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antioxidants and zinc in age-related macular degeneration (disease progression) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Patterned dystrophy of retinal pigment epithelium Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Patterned dystrophy of retinal pigment epithelium phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Rhegmatogenous retinal detachment, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Rhegmatogenous retinal detachment, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal cone dystrophy 3B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal cone dystrophy 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, early-onset severe Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, early-onset severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
retinal dimer Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical retinal dimer from the curated CTD Gene-Chemical Interactions dataset.
9-cis-retinal Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical 9-cis-retinal from the curated CTD Gene-Chemical Interactions dataset.

Harmonizome 3.0

progressive retinal degeneration Gene Set

macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set

eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set

frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set

basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set

chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency Gene Set

multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene Set

alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set

progressive cone degeneration Gene Set

Progressive rod-cone degeneration protein Gene Set

Progressive Cerebellar Degeneration Gene Set

Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts Gene Set

Skeletal dysplasia and progressive central nervous system degeneration Gene Set

Generalized Progressive Retinal Atrophy Gene Set

Progressive Retinal Atrophy Gene Set

Progressive retinal dystrophy due to retinol transport defect Gene Set

Retinal degeneration, autosomal recessive, clumped pigment type Gene Set

Retinal Degeneration Gene Set

Late-Onset Retinal Degeneration Gene Set

retinal degeneration Gene Set

retinal degeneration Gene Set

peripheral retinal degeneration Gene Set

retinal degeneration Gene Set

blind vision; blindness; retinal degeneration Gene Set

adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set

geographic atrophy; macular degeneration; retinal drusen Gene Set

retinal degeneration Gene Set

blindness; retinal degeneration Gene Set

choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set

choroidal neovascularization; macular degeneration; retinal drusen Gene Set

retinal degeneration; retinitis pigmentosa Gene Set

color vision defects; retinal degeneration Gene Set

diseases in twins; macular degeneration; retinal drusen Gene Set

choroidal neovascularization; retinal drusen; wet macular degeneration Gene Set

retinal degeneration Gene Set

retinal degeneration Gene Set

pigmentary retinal degeneration Gene Set

honeycomb retinal degeneration Gene Set

cystic retinal degeneration Gene Set

Retinal Degeneration Gene Set

Retinal degeneration protein 3 Gene Set

retinal degeneration Gene Set

retinal outer nuclear layer degeneration Gene Set

retinal rod cell degeneration Gene Set

retinal cone cell degeneration Gene Set

retinal ganglion cell degeneration Gene Set

retinal photoreceptor degeneration Gene Set

retinal degeneration, late-onset, autosomal dominant Gene Set

infantile cerebellar-retinal degeneration Gene Set

retinal degeneration, autosomal recessive, clumped pigment type Gene Set

Infantile Cerebellar-Retinal Degeneration Gene Set

Late-Onset Retinal Degeneration (Disorder) Gene Set

Cystoid Macular Retinal Degeneration Gene Set

Glaucomatous Retinal Degeneration Gene Set

Retinal Lattice Degeneration Gene Set

Retinal Degeneration Gene Set

Peripheral Retinal Degeneration Gene Set

Retinal Degeneration Gene Set

Retinal Pigmentary Degeneration Gene Set

Peripheral Cystoid Retinal Degeneration Gene Set

Retinal degeneration Gene Set

Retinal degeneration Gene Set

Retinal degeneration Gene Set

Retinal lattice degeneration Gene Set

Peripheral retinal degeneration Gene Set

late-onset retinal degeneration Gene Set

Infantile cerebellar-retinal degeneration Gene Set

Cobblestone retinal degeneration Gene Set

Late-onset retinal degeneration Gene Set

Retinal degeneration Gene Set

Infantile cerebellar-retinal degeneration Gene Set

Lattice retinal degeneration Gene Set

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

activated protein c resistance; retinal neovascularization; retinal vein occlusion Gene Set

behcet syndrome; retinal artery occlusion; retinal vein occlusion Gene Set

atherosclerosis; pregnancy complications, cardiovascular; pregnancy complications, hematologic; retinal artery occlusion; retinal vein occlusion; thrombophilia; thrombosis Gene Set

retinal artery occlusion; retinal vein occlusion Gene Set

?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene Set

Retinal detachment or retinal break Gene Set