Periodontal Atrophy

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Results for "Periodontal Atrophy": 674 gene sets

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Periodontal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
aggressive periodontitis; dental plaque; periodontal attachment loss; periodontal diseases; periodontal pocket Gene Set From GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; dental plaque; periodontal attachment loss; periodontal diseases; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gingival recession; gingivitis; periodontal attachment loss; periodontal diseases; periodontal pocket Gene Set From GAD Gene-Disease Associations genes associated with the disease gingival recession; gingivitis; periodontal attachment loss; periodontal diseases; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aggressive periodontitis; chronic periodontitis; periodontal attachment loss; periodontal pocket Gene Set From GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; chronic periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; periodontal attachment loss; periodontal pocket Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic periodontitis; periodontal attachment loss; periodontal pocket Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aggressive periodontitis; periodontal attachment loss; periodontal pocket Gene Set From GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile Gene Set From GAD Gene-Disease Associations genes associated with the disease aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal; spinal muscular atrophies of childhood; spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophies, hereditary; optic atrophy, autosomal dominant; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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.
Periodontal Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Periodontal Diseases from the curated CTD Gene-Disease Associations dataset.
periodontal disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease periodontal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
periodontal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease periodontal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
alveolar bone loss; periodontal attachment loss; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
periodontal diseases; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease periodontal diseases; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
periodontal attachment loss; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease periodontal attachment loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; periodontal attachment loss; tooth loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; periodontal attachment loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular disease; periodontal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; periodontal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
behcet syndrome; periodontal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease behcet syndrome; periodontal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 1; periodontal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 1; periodontal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fetal growth retardation; periodontal diseases; pregnancy complications Gene Set From GAD Gene-Disease Associations genes associated with the disease fetal growth retardation; periodontal diseases; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
periodontal attachment loss; periodontitis; tooth mobility Gene Set From GAD Gene-Disease Associations genes associated with the disease periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
periodontal disease Gene Set From GAD Gene-Disease Associations genes associated with the disease periodontal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gingival hemorrhage; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease gingival hemorrhage; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility Gene Set From GAD Gene-Disease Associations genes associated with the disease dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss Gene Set From GAD Gene-Disease Associations genes associated with the disease alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
crohn disease; crohn's disease; periodontal pocket; periodontitis Gene Set From GAD Gene-Disease Associations genes associated with the disease crohn disease; crohn's disease; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
periodontal diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease periodontal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
periodontal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term periodontal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Periodontal disease-related phenotypes Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Periodontal disease-related phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Periodontal microbiota Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Periodontal microbiota phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
periodontal disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease periodontal disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
Periodontal Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Periodontal Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Periodontal Attachment Loss Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Periodontal Attachment Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Periodontal Pocket Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Periodontal Pocket phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
periodontal ligament hypercellularity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the periodontal ligament hypercellularity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal periodontal ligament morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal periodontal ligament morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
periodontal ligament Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue periodontal ligament from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
periodontal ligament Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue periodontal ligament in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Periodontal Pocket Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Pocket in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periodontal Inflammation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Inflammation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periodontal Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periodontal Attachment Loss Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Attachment Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periodontal Abscess Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodontal Abscess in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
abnormal periodontal ligament morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal periodontal ligament morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
periodontal ligament hypercellularity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the periodontal ligament hypercellularity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
periodontal ligament necrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the periodontal ligament necrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
periodontal pocket Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the periodontal pocket phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Periodontal ligament stem cell_Periodontal ligament_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Periodontal ligament stem cell_Periodontal ligament_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Periodontal disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Periodontal disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Periodontal disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Periodontal disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Periodontal ligament Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Periodontal ligament from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Periodontal ligament Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Periodontal ligament in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Periodontal ligament cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Periodontal ligament cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Periodontal disease-related phenotype (Socransky) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periodontal disease-related phenotype (Socransky) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Periodontal disease related phenotype (PCT3) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periodontal disease related phenotype (PCT3) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Periodontal disease related phenotype (PCT5) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periodontal disease related phenotype (PCT5) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Periodontal microbiota Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Periodontal microbiota phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Bosch-boonstra-schaaf optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy 7 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Dominant hereditary optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Dominant hereditary optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, type II Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, X-linked 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
X-linked myopathy with postural muscle atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the X-linked myopathy with postural muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic atrophy and cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Optic Atrophy Type 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Optic Atrophy Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Spinal muscular atrophy, lower extremity predominant 1, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hereditary motor and sensory neuropathy with optic atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hereditary motor and sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcornea, myopic chorioretinal atrophy, and telecanthus 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.
Congenital microvillous atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Congenital microvillous atrophy 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.
Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, autosomal recessive 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sveinsson Chorioretinal Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Sveinsson Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy, Hereditary, Leber Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Hereditary, Leber from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy, Jerash type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy, Jerash type from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 1 and deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 1 and deafness from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 7 from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy 4 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Spinal muscular atrophy 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy 4 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 5 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.
Spinal muscular atrophy with respiratory distress 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal muscular atrophy with respiratory distress 1 from the curated CTD Gene-Disease Associations dataset.
Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Atrophy from the curated CTD Gene-Disease Associations dataset.
Muscular Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy from the curated CTD Gene-Disease Associations dataset.
Myopathy, X-Linked, With Postural Muscle Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, X-Linked, With Postural Muscle Atrophy from the curated CTD Gene-Disease Associations dataset.
Costeff optic atrophy syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Costeff optic atrophy syndrome from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy polyneuropathy deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy polyneuropathy deafness from the curated CTD Gene-Disease Associations dataset.
Spastic Paraplegia, Optic Atrophy, and Neuropathy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, and Neuropathy from the curated CTD Gene-Disease Associations dataset.
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.
Optic atrophy 6 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy 6 from the curated CTD Gene-Disease Associations dataset.
Optic atrophy and cataract, autosomal dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic atrophy and cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.
Gyrate Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gyrate Atrophy from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy from the curated CTD Gene-Disease Associations dataset.
Pigmented Paravenous Chorioretinal Atrophy Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Paravenous Chorioretinal Atrophy from the curated CTD Gene-Disease Associations dataset.
OPTIC ATROPHY 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease OPTIC ATROPHY 2 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY from the curated CTD Gene-Disease Associations dataset.
Optic Atrophy, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Optic Atrophy, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Muscular Atrophy, Spinal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Atrophy, Spinal from the curated CTD Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinal muscular atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dentatorubral-pallidoluysian atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
multiple system atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
adult spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrophy of prostate Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of prostate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
juvenile spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intermediate spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
primary optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skin atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
atrophy of testis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple system atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
hereditary choroidal atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
partial optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease partial optic atrophy 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.
olivopontocerebellar atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease olivopontocerebellar atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
survival motor neuron spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
gyrate atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gyrate atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 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.
alzheimer disease; atrophy; dementia; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy; pulmonary disease, chronic obstructive Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy; pulmonary disease, chronic obstructive 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.
atrophy; gastritis; helicobacter infections; metaplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; metaplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; geographic atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
posterior cortical atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease posterior cortical atrophy 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.
atrophy; helicobacter infections; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; helicobacter infections Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; helicobacter infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; prenatal exposure delayed effects; substance-related disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; prenatal exposure delayed effects; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic disc atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease optic disc atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
gyrate atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease gyrate atrophy 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.
atrophy; dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; peptic ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blindness; optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease blindness; optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; dyspepsia; gastritis; helicobacter infections; peptic ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; precancerous conditions; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm Gene Set From GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; atrophy; esophageal neoplasms; gastroesophageal reflux; helicobacter infections; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; brain diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; brain diseases 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.
atrophy; gastritis; inflammation Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; inflammation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
muscular atrophy, spinal Gene Set From GAD Gene-Disease Associations genes associated with the disease muscular atrophy, spinal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; duodenal ulcer; helicobacter infections; peptic ulcer; stomach ulcer; stomach; ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; aphasia; atrophy; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; aphasia; atrophy; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; dna damage; gastritis, atrophic; metaplasia; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting 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.
gastric atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease gastric atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy, hereditary, leber Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal muscular atrophy phenotype Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal muscular atrophy phenotype in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy, hereditary, leber; vision disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy, hereditary, leber; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; amnesia; atrophy; Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; amnesia; atrophy; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
stomach cancer; stomach atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease stomach cancer; stomach atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alcoholism; atrophy; brain diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alcoholism; atrophy; brain diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; epilepsy; hyperhomocysteinemia Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; epilepsy; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
optic atrophy and moderate deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease optic atrophy and moderate deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; atrophy; disease progression Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; atrophy; disease progression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; gastritis; helicobacter infections; stomach neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; gastritis; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
schizophrenia; brain atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease schizophrenia; brain atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; huntington disease Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hippocampal atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease hippocampal atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dystonic disorders; multiple system atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term atrophy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 Gene Set From GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Spinal Muscular Atrophy, Infantile_CNS - Spinal Cord (MMHCC)_GSE3075 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.
skeletal muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
striated muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
muscle atrophy Gene Set From GO Biological Process Annotations 2015 genes participating in the muscle atrophy biological process from the curated GO Biological Process Annotations 2015 dataset.
MRI atrophy measures Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the MRI atrophy measures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Hippocampal atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Hippocampal atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
muscular atrophy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease muscular atrophy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
motor neuron atrophy Gene Set From GWASdb SNP-Phenotype Associations genes associated with the motor neuron atrophy 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.
type 2 muscle fiber atrophy Gene Set From HPO Gene-Disease Associations genes associated with the type 2 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
levator palpebrae superioris atrophy Gene Set From HPO Gene-Disease Associations genes associated with the levator palpebrae superioris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral white matter atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral white matter atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease 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.
cerebellar cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar cortical atrophy 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.
generalized limb muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the generalized limb muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
global brain atrophy Gene Set From HPO Gene-Disease Associations genes associated with the global brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral retinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripheral retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
caudate atrophy Gene Set From HPO Gene-Disease Associations genes associated with the caudate atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
corpus callosum atrophy Gene Set From HPO Gene-Disease Associations genes associated with the corpus callosum atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tubular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the tubular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thenar muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the thenar muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pontocerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the pontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
brain atrophy Gene Set From HPO Gene-Disease Associations genes associated with the brain atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
skeletal muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the skeletal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tongue atrophy Gene Set From HPO Gene-Disease Associations genes associated with the tongue atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
olivopontocerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the olivopontocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic atrophy Gene Set From HPO Gene-Disease Associations genes associated with the optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dermal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the dermal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripapillary chorioretinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripapillary chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
frontal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the frontal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subcortical cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the subcortical cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
muscle fiber atrophy Gene Set From HPO Gene-Disease Associations genes associated with the muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse skin atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse skin atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hand muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the hand muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
motor neuron atrophy Gene Set From HPO Gene-Disease Associations genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pelvic girdle muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the pelvic girdle muscle atrophy 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.
cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
leber optic atrophy Gene Set From HPO Gene-Disease Associations genes associated with the leber optic atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral axonal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peripheral axonal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal pigment epithelial atrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal pigment epithelial atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fundus atrophy Gene Set From HPO Gene-Disease Associations genes associated with the fundus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
scapular muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the scapular muscle atrophy 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.
first dorsal interossei muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the first dorsal interossei muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive muscular atrophy 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.
optic atrophy from cranial nerve compression Gene Set From HPO Gene-Disease Associations genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar vermis atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
villous atrophy Gene Set From HPO Gene-Disease Associations genes associated with the villous atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
iris atrophy Gene Set From HPO Gene-Disease Associations genes associated with the iris atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy of alveolar ridges Gene Set From HPO Gene-Disease Associations genes associated with the atrophy of alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the renal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the spinal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
interosseus muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the interosseus muscle atrophy 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.
type 1 muscle fiber atrophy Gene Set From HPO Gene-Disease Associations genes associated with the type 1 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebral cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
superior rectus atrophy Gene Set From HPO Gene-Disease Associations genes associated with the superior rectus atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
noninflammatory macular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the noninflammatory macular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized cerebral atrophy/hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb-girdle muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the limb-girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
testicular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the testicular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
shoulder girdle muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the shoulder girdle muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pigmented paravenous chorioretinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the renal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peroneal muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the peroneal muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy of the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the atrophy of the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
chorioretinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the chorioretinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
frontotemporal cerebral atrophy Gene Set From HPO Gene-Disease Associations genes associated with the frontotemporal cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy of the dentate nucleus Gene Set From HPO Gene-Disease Associations genes associated with the atrophy of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
quadriceps muscle atrophy Gene Set From HPO Gene-Disease Associations genes associated with the quadriceps muscle atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinocerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the spinocerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal atrophy Gene Set From HPO Gene-Disease Associations genes associated with the retinal atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
temporal cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the temporal cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Multiple System Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy, Hereditary, Leber Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Hereditary, Leber phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy, Autosomal Dominant Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy, Autosomal Dominant phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Atrophy, Spinal Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy, Spinal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Optic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Muscular Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Muscular Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Geographic Atrophy Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Geographic Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Optic atrophy 3-like Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Optic atrophy 3-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.
dentatorubropallidoluysian atrophy Gene Set From KEGG Pathways proteins participating in the dentatorubropallidoluysian atrophy pathway from the KEGG Pathways dataset.
ovary atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ovary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle fiber atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney cortex atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney cortex atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
testicular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the testicular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney collecting duct atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thymus atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thymus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
brain atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the brain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal pigment epithelium atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal pigment epithelium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
sebaceous gland atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the sebaceous gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
midbrain atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal tubule atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
seminal vesicle atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the seminal vesicle atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
renal glomerulus atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
meibomian gland atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the meibomian gland atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
uterus atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the uterus atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreatic acinar cell atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreatic acinar cell atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
endometrium atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the endometrium atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
epidermal atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the epidermal atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
exocrine pancreas atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spleen atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spleen atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
iris atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the iris atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vagina atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vagina atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induced muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased susceptibility to induced muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vulva atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vulva atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscular atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pancreas atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
oviduct atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the oviduct atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
external male genitalia atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney medulla atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney medulla atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney papillary atrophy Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 6 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 5 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 1 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy-4 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy-4 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.
spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, x-linked 2, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, x-linked 2, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-2 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-2 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-3 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-1 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-1 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy-4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy-4 phenotype from the curated OMIM Gene-Disease Associations dataset.
{multiple system atrophy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, x-linked, with postural muscle atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, x-linked, with postural muscle atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, chronic distal, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, jokela type Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, jokela type phenotype from the curated OMIM Gene-Disease Associations dataset.
sveinsson choreoretinal atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the sveinsson choreoretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
scapuloperoneal spinal muscular atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the scapuloperoneal spinal muscular atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, late-onset, finkel type Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, late-onset, finkel type phenotype from the curated OMIM Gene-Disease Associations dataset.
dentatorubro-pallidoluysian atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the dentatorubro-pallidoluysian atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
{spinal muscular atrophy, type iii, modifier of} Gene Set From OMIM Gene-Disease Associations genes associated with the {spinal muscular atrophy, type iii, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy-7 Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy-7 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, lower extremity-predominant 1, ad Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant 1, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
spastic paraplegia, optic atrophy, and neuropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spastic paraplegia, optic atrophy, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
bosch-boonstra-schaaf optic atrophy syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the bosch-boonstra-schaaf optic atrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 2, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 2, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
gyrate atrophy of choroid and retina with or without ornithinemia Gene Set From OMIM Gene-Disease Associations genes associated with the gyrate atrophy of choroid and retina with or without ornithinemia phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy 3 with cataract Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy 3 with cataract phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, lower extremity-predominant, 2, ad Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, lower extremity-predominant, 2, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
microcornea, myopic chorioretinal atrophy, and telecanthus Gene Set From OMIM Gene-Disease Associations genes associated with the microcornea, myopic chorioretinal atrophy, and telecanthus phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, x-linked 3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set From OMIM Gene-Disease Associations genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.
pigmented paravenous chorioretinal atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the pigmented paravenous chorioretinal atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
?neurodegeneration with optic atrophy, childhood onset Gene Set From OMIM Gene-Disease Associations genes associated with the ?neurodegeneration with optic atrophy, childhood onset phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal and bulbar muscular atrophy of kennedy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal and bulbar muscular atrophy of kennedy phenotype from the curated OMIM Gene-Disease Associations dataset.
optic atrophy plus syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the optic atrophy plus syndrome 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.
spinal muscular atrophy, distal, congenital nonprogressive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.
{leber optic atrophy, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {leber optic atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Geographic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Geographic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bulbo-Spinal Atrophy, X-Linked Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bulbo-Spinal Atrophy, X-Linked in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Pigment Epithelium Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Pigment Epithelium Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebral Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Linear Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Linear Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Brain Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Brain Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Testis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Testis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Olivopontocerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Infantile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Infantile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Limb Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Limb Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscle Fiber Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscle Fiber Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Motor Neuron Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Motor Neuron Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subcortical Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subcortical Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sveinsson Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sveinsson Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Kidney Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Kidney in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Villous Atrophy Of Intestine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Villous Atrophy Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations 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.
Frontotemporal Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontotemporal Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Cerebral Atrophy/Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Cerebral Atrophy/Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dentatorubral-Pallidoluysian Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dentatorubral-Pallidoluysian Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy, Disuse Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Disuse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of The Spinal Cord Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Corpus Callosum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Corpus Callosum 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.
Cerebral White Matter Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebral White Matter Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Prostate Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Prostate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pelvic Girdle Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pelvic Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy, Muscular, Spinobulbar Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy, Muscular, Spinobulbar in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proliferative Inflammatory Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proliferative Inflammatory Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gyrate Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy 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.
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.
Frontal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy, Cerebellar Variant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Optic Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Optic Disc 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.
Cerebellar Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dominant Hereditary Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dominant Hereditary Optic 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 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.
Atrophy Of Liver Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acquired Atrophy Of Ovary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acquired Atrophy Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Pancreas Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Tongue Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paravenous Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paravenous Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pigmented Paravenous Chorioretinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pigmented Paravenous Chorioretinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limb-Girdle Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Limb-Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Posterior Cortical Atrophy Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Posterior Cortical Atrophy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Vagina Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Vagina in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Urogenital Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Urogenital Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peroneal Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peroneal Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
Auditory Neuropathy And Optic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Auditory Neuropathy And Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Diffuse Skin Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Diffuse Skin Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cervical Spinal Cord Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cervical Spinal Cord Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Splenic Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Splenic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Atrophy Of Thyroid Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Atrophy Of Thyroid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sporadic Olivopontocerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sporadic Olivopontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Axonal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Axonal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Tongue Papillae Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Tongue Papillae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pancreatic Acinar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pancreatic Acinar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Tubular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Tubular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glaucomatous Atrophy Of Optic Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glaucomatous Atrophy Of Optic Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leber Optic Atrophy And Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leber Optic Atrophy And Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy Of Seminal Vesicle Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy Of Seminal Vesicle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripapillary Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripapillary Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Gyrate Atrophy Of Choroid And Retina With Pyridoxine-Responsive Ornithinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Optic Atrophy Plus Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Optic Atrophy Plus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Cortical Cerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Cortical Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rectus Femoris Muscle Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rectus Femoris Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Parietal Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Parietal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Oculopharyngeal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Oculopharyngeal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
Scapuloperoneal Form Of Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Scapuloperoneal Form Of Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Cerebral Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonprogressive Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonprogressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Skeletal Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skeletal Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Foveal Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foveal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Pigment Epithelial Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigment Epithelial Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hippocampal Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hippocampal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Muscle Atrophy Due To Neurologic Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Atrophy Due To Neurologic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hand Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Shoulder Girdle Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shoulder Girdle Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Global Brain Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Global Brain Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Choriocapillaris Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Choriocapillaris Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mucosal Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mucosal Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Villous Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Villous Atrophy 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.
Atrophy Of Quadriceps Femoris Muscle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Quadriceps Femoris Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscle Fiber Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Fiber Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Neurogenic Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurogenic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple System Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Cerebral Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebral Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy Of The Dentate Nucleus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of The Dentate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Corticospinal Tract Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corticospinal Tract Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Purkinje Layer Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Purkinje Layer Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Vermis Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Vermis Atrophy 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.
Extremity Muscle Atrophy, Lower Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Extremity Muscle Atrophy, Lower in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Caudate Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caudate Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
First Dorsal Interossei Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype First Dorsal Interossei Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thenar Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thenar Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Cerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy Of Alveolar Ridges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Alveolar Ridges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Optic Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Optic Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Scapular Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scapular Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intrinsic Hand Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intrinsic Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pontocerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pontocerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tubular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tubular Atrophy Assessment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tubular Atrophy Assessment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripapillary Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripapillary Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tibialis Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tibialis Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fundus Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fundus Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Levator Palpebrae Superioris Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Levator Palpebrae Superioris Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Superior Rectus Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Superior Rectus Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Frontal Lobe Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Frontal Lobe Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axial Muscle Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axial Muscle Atrophy 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 Of Vas Deferens Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy Of Vas Deferens in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
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.
skeletal muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
striated muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2023 dataset.
muscular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Meibomian gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Meibomian gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
renal glomerulus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the renal glomerulus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
temporal lobe atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the temporal lobe atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
alveolar process atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the alveolar process atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
testicular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the testicular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thymus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thymus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spleen atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spleen atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
renal tubule atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the renal tubule atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pancreatic acinar cell atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreatic acinar cell atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lacrimal gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lacrimal gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney cortex atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney cortex atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ovary atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
uterus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the uterus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
external male genitalia atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the external male genitalia atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vulva atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vulva atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vagina atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vagina atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
endometrium atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the endometrium atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney collecting duct atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney collecting duct atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney medulla atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney medulla atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thymus cortex atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thymus cortex atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle fiber atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle fiber atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cerebellum atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebellum atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Leydig cell atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Leydig cell atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic nerve atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic nerve atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina pigment epithelium atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina pigment epithelium atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
seminal vesicle atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the seminal vesicle atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
sebaceous gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the sebaceous gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased susceptibility to induced muscular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
midbrain atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the midbrain atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
epidermal atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the epidermal atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney papillary atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney papillary atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
brain atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the brain atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
exocrine pancreas atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the exocrine pancreas atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hippocampus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hippocampus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
oviduct atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the oviduct atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thymus medulla atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thymus medulla atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
facial muscle atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the facial muscle atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Harderian gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Harderian gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
iris atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the iris atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
gastric gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the gastric gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skin atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skin atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased susceptibility to induced muscular atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lymph node atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lymph node atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small intestinal villus atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small intestinal villus atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
forebrain atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the forebrain atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
striatum atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the striatum atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
adrenal gland atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the adrenal gland atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pancreas atrophy Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas atrophy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle atrophy Gene Set From GO Biological Process Annotations 2025 genes participating in the skeletal muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset.
striated muscle atrophy Gene Set From GO Biological Process Annotations 2025 genes participating in the striated muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of muscle atrophy Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of muscle atrophy biological process from the curated GO Biological Process Annotations 2025 dataset.
Spinal muscular atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease dentatorubral-pallidoluysian atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Multiple system atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Multiple system atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked spinal muscular atrophy 2 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked spinal muscular atrophy 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with lower extremity predominant from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Optic atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Optic atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Optic atrophy 3 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Optic atrophy 3 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.
Gyrate atrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Gyrate atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Skin atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skin atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Atrophy of testis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrophy of testis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gyrate atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gyrate atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Childhood spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Childhood spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Dominant optic atrophy plus syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Dominant optic atrophy plus syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
dentatorubral-pallidoluysian atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease dentatorubral-pallidoluysian atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple system atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Adult spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Adult spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Scapuloperoneal spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Scapuloperoneal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with progressive myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hereditary choroidal atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hereditary choroidal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with lower extremity predominant in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
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.
Olivopontocerebellar atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Olivopontocerebellar atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sveinsson chorioretinal atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sveinsson chorioretinal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intermediate spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intermediate spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Bosch-Boonstra-Schaaf optic atrophy syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bosch-Boonstra-Schaaf optic atrophy syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Partial optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar atrophy, visual impairment, and psychomotor retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar atrophy, visual impairment, and psychomotor retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pigmented paravenous chorioretinal atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pigmented paravenous chorioretinal atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset neurodegeneration with brain atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset neurodegeneration with brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary optic atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
childhood-onset dystonia with optic atrophy and basal ganglia abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease childhood-onset dystonia with optic atrophy and basal ganglia abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked distal spinal muscular atrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked distal spinal muscular atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked spinal muscular atrophy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked spinal muscular atrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Juvenile spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Juvenile spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant adult-onset proximal spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant adult-onset proximal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction 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.
Atrophy of prostate Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Atrophy of prostate in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy, Jokela type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy, Jokela type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Optic atrophy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Optic atrophy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy type 0 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy type 0 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with lower extremity predominant 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with lower extremity predominant 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gyrate atrophy of choroid and retina Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Gyrate atrophy of choroid and retina phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive optic atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple system atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple system atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal pigment epithelial atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal pigment epithelial atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Adult-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Scapuloperoneal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapuloperoneal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant optic atrophy classic form Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant optic atrophy classic form phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
OPA1-related optic atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the OPA1-related optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pigmented paravenous retinochoroidal atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pigmented paravenous retinochoroidal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hand muscle atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hand muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant childhood-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy-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.
Short stature-optic atrophy-Pelger-Huet anomaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-optic atrophy-Pelger-Huet anomaly syndrome 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.
Retinal atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Bosch-Boonstra-Schaaf optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Bosch-Boonstra-Schaaf optic atrophy syndrome 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.
Cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Brain atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinocerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinocerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Limb-girdle muscle atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb-girdle muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital microvillous atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Testicular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Testicular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile-onset X-linked spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile-onset X-linked spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral cortical atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral cortical atrophy 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.
Auditory neuropathy-optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Auditory neuropathy-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Microcornea-myopic chorioretinal atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcornea-myopic chorioretinal atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Leber optic atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Leber optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dentatorubral-pallidoluysian atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dentatorubral-pallidoluysian atrophy 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.
Posterior cortical atrophy and Alzheimer's disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Posterior cortical atrophy and Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple system atrophy (pathologically confirmed) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple system atrophy (pathologically confirmed) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple system atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Multiple system atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hippocampal atrophy rate Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hippocampal atrophy rate phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hippocampal atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hippocampal atrophy 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.
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.
Severe gastric atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Severe gastric atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Gastric atrophy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Gastric atrophy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Periodontal Atrophy Gene Set

aggressive periodontitis; dental plaque; periodontal attachment loss; periodontal diseases; periodontal pocket Gene Set

gingival recession; gingivitis; periodontal attachment loss; periodontal diseases; periodontal pocket Gene Set

alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

aggressive periodontitis; chronic periodontitis; periodontal attachment loss; periodontal pocket Gene Set

dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

alveolar bone loss; periodontal attachment loss; periodontal pocket Gene Set

chronic periodontitis; periodontal attachment loss; periodontal pocket Gene Set

alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket Gene Set

aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

aggressive periodontitis; periodontal attachment loss; periodontal pocket Gene Set

aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile Gene Set

muscular atrophy, spinal; spinal muscular atrophy Gene Set

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

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

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

Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene Set

Periodontal Diseases Gene Set

periodontal disease Gene Set

periodontal disease Gene Set

alveolar bone loss; periodontal attachment loss; periodontitis Gene Set

alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set

periodontal diseases; periodontitis Gene Set

periodontal attachment loss; periodontitis Gene Set

alveolar bone loss; periodontal attachment loss; tooth loss Gene Set

cardiovascular disease; periodontal disease Gene Set

behcet syndrome; periodontal diseases Gene Set

diabetes mellitus, type 1; periodontal diseases Gene Set

fetal growth retardation; periodontal diseases; pregnancy complications Gene Set

periodontal attachment loss; periodontitis; tooth mobility Gene Set

periodontal disease Gene Set

gingival hemorrhage; periodontal pocket; periodontitis Gene Set

dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility Gene Set

periodontal pocket; periodontitis Gene Set

alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss Gene Set

crohn disease; crohn's disease; periodontal pocket; periodontitis Gene Set

periodontal diseases Gene Set

periodontal Gene Set

Periodontal disease-related phenotypes Gene Set

Periodontal microbiota Gene Set

periodontal disease Gene Set

Periodontal Diseases Gene Set

Periodontal Attachment Loss Gene Set

Periodontal Pocket Gene Set

periodontal ligament hypercellularity Gene Set

abnormal periodontal ligament morphology Gene Set

periodontal ligament Gene Set

periodontal ligament Gene Set

Periodontal Pocket Gene Set

Periodontal Inflammation Gene Set

Periodontal Infection Gene Set

Periodontal Attachment Loss Gene Set

Periodontal Abscess Gene Set

abnormal periodontal ligament morphology Gene Set

periodontal ligament hypercellularity Gene Set

periodontal ligament necrosis Gene Set

periodontal pocket Gene Set

Periodontal ligament stem cell_Periodontal ligament_Human Gene Set

Periodontal disease Gene Set

Periodontal disease Gene Set

Periodontal ligament Gene Set

Periodontal ligament Gene Set

Periodontal ligament cell Gene Set

Periodontal disease-related phenotype (Socransky) Gene Set

Periodontal disease related phenotype (PCT3) Gene Set

Periodontal disease related phenotype (PCT5) Gene Set

Periodontal microbiota Gene Set

Bosch-boonstra-schaaf optic atrophy syndrome Gene Set

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

Optic atrophy 7 Gene Set

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

Dominant hereditary optic atrophy Gene Set

Spinal muscular atrophy, type II Gene Set

Distal spinal muscular atrophy, X-linked 3 Gene Set

Gyrate atrophy of choroid and retina with pyridoxine-responsive ornithinemia Gene Set

Spinal muscular atrophy Gene Set

X-linked myopathy with postural muscle atrophy Gene Set