Intellectual disability, progressive

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Results for "Intellectual disability, progressive": 751 gene sets

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intellectual disability, progressive Gene Set From HPO Gene-Disease Associations genes associated with the intellectual disability, progressive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Intellectual Disability, Progressive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intellectual Disability, Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Intellectual Disability And Progressive Spastic Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Intellectual Disability And Progressive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Severe intellectual disability-progressive spastic diplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-progressive spastic diplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Blepharophimosis-ptosis-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Blepharophimosis-ptosis-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Coffin Siris/Intellectual Disability Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Coffin Siris/Intellectual Disability phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Syndromic intellectual disability Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Syndromic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Intellectual Disability Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intellectual Disability from the curated CTD Gene-Disease Associations dataset.
syndromic intellectual disability Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease syndromic intellectual disability from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
intellectual disability Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease intellectual disability from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
syndromic intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease syndromic intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
non-syndromic intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease non-syndromic intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
intellectual disability, moderate Gene Set From HPO Gene-Disease Associations genes associated with the intellectual disability, moderate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intellectual disability, severe Gene Set From HPO Gene-Disease Associations genes associated with the intellectual disability, severe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intellectual disability, profound Gene Set From HPO Gene-Disease Associations genes associated with the intellectual disability, profound phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intellectual disability, mild Gene Set From HPO Gene-Disease Associations genes associated with the intellectual disability, mild phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intellectual disability Gene Set From HPO Gene-Disease Associations genes associated with the intellectual disability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Intellectual Disability Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Intellectual Disability phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
blepharophimosis-ptosis-intellectual disability syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the blepharophimosis-ptosis-intellectual disability syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Severe Intellectual Disability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Severe Intellectual Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Moderate Intellectual Disability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Moderate Intellectual Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Borderline Intellectual Disability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Borderline Intellectual Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ahdc1-Related Intellectual Disability, Obstructive Sleep Apnea, Mild Dysmorphism Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ahdc1-Related Intellectual Disability, Obstructive Sleep Apnea, Mild Dysmorphism Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hivep2-Related Intellectual Disability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hivep2-Related Intellectual Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intellectual Disability Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intellectual Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Intellectual disability Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Intellectual disability from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked intellectual disability-psychosis-macroorchidism syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked intellectual disability-psychosis-macroorchidism syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Syndromic X-linked intellectual disability from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Lubs type Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Syndromic X-linked intellectual disability Lubs type from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Syndromic intellectual disability Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Syndromic intellectual disability from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Snyder type Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Syndromic X-linked intellectual disability Snyder type from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Siderius type Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Syndromic X-linked intellectual disability Siderius type from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Alpha thalassemia-X-linked intellectual disability syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Alpha thalassemia-X-linked intellectual disability syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability 94 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability 94 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 99 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 99 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Shashi type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Shashi type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual disability-severe speech delay-mild dysmorphism syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual disability-severe speech delay-mild dysmorphism syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Alpha thalassemia-intellectual disability syndrome type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alpha thalassemia-intellectual disability syndrome type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Cabezas type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Cabezas type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Pilorge type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Pilorge type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Lubs type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Lubs type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked intellectual disability-psychosis-macroorchidism syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked intellectual disability-psychosis-macroorchidism syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Stocco Dos Santos type X-linked intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Stocco Dos Santos type X-linked intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 98 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 98 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 91 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 91 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 58 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 58 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
deafness-intellectual disability, Martin-Probst type syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease deafness-intellectual disability, Martin-Probst type syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Claes-Jensen type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Claes-Jensen type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability type 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability type 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Najm type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Najm type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Snyder type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Snyder type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Turner type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Turner type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Alpha thalassemia-X-linked intellectual disability syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Alpha thalassemia-X-linked intellectual disability syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Siderius type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Siderius type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 81 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 81 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 63 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 63 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Uveal coloboma-cleft lip and palate-intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Uveal coloboma-cleft lip and palate-intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 106 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 106 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 30 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 30 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 101 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 101 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 103 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 103 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 90 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 90 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital muscular dystrophy with cataracts and intellectual disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital muscular dystrophy with cataracts and intellectual disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
female-restricted syndromic X-linked intellectual disability 99 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease female-restricted syndromic X-linked intellectual disability 99 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Raymond type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Raymond type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked intellectual disability-short stature-overweight syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked intellectual disability-short stature-overweight syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 92 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 92 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Hedera type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Hedera type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 97 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 97 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability Nascimento type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability Nascimento type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 93 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 93 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 89 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 89 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 72 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 72 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 77 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 77 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual disability 34 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual disability 34 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 107 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 107 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability ARX-related Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability ARX-related in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 73 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 73 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual disability 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual disability 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Marfanoid habitus and intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Marfanoid habitus and intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hyperphosphatasia-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hyperphosphatasia-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hirschsprung disease-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hirschsprung disease-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic X-linked intellectual disability Raymond Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic X-linked intellectual disability Raymond phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic X-linked intellectual disability Hedera Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic X-linked intellectual disability Hedera phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked intellectual disability Cabezas Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked intellectual disability Cabezas phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Blepharophimosis - intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Blepharophimosis - intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic X-linked intellectual disability Najm Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic X-linked intellectual disability Najm phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic X-linked intellectual disability Snyder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic X-linked intellectual disability Snyder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alpha thalassemia-X-linked intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Alpha thalassemia-X-linked intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-hypotonic facies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-hypotonic facies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked intellectual disability-psychosis-macroorchidism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked intellectual disability-psychosis-macroorchidism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic X-linked intellectual disability Lubs Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic X-linked intellectual disability Lubs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant non-syndromic intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant non-syndromic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alopecia-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Alopecia-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-severe speech delay-mild dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-severe speech delay-mild dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability and myopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability and myopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Rare genetic intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rare genetic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CTCF-related syndromic intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CTCF-related syndromic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-hypotonia-spasticity-sleep disorder syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-hypotonia-spasticity-sleep disorder syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Alpha-thalassemia/intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Alpha-thalassemia/intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic X-linked intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic X-linked intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked intellectual disability-cerebellar hypoplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked intellectual disability-cerebellar hypoplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic X-linked intellectual disability Claes-Jensen Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic X-linked intellectual disability Claes-Jensen phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Coffin Siris/Intellectual Disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Coffin Siris/Intellectual Disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-epilepsy-extrapyramidal syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-epilepsy-extrapyramidal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
DYRK1A-related intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the DYRK1A-related intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability-strabismus syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability-strabismus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-syndromic X-linked intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-syndromic X-linked intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
UPF3B-associated intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the UPF3B-associated intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual disability and seizures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual disability and seizures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked intellectual disability-hypotonia-movement disorder syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked intellectual disability-hypotonia-movement disorder syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic X-linked intellectual disability Siderius Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic X-linked intellectual disability Siderius phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MED12-related intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MED12-related intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebral visual impairment and intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebral visual impairment and intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TELO2-related intellectual disability-neurodevelopmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TELO2-related intellectual disability-neurodevelopmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Gnb5-related intellectual disability-cardiac arrhythmia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Gnb5-related intellectual disability-cardiac arrhythmia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GATAD2B-related intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GATAD2B-related intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked intellectual disability-short stature-overweight syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked intellectual disability-short stature-overweight syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ZC4H2-related X-linked intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ZC4H2-related X-linked intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ACTL6B-related dominant intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ACTL6B-related dominant intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ZSWIM6 related intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ZSWIM6 related intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Microcephaly-thin corpus callosum-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Microcephaly-thin corpus callosum-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Rare syndromic intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Rare syndromic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SIN3A-related intellectual disability syndrome due to a point mutation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SIN3A-related intellectual disability syndrome due to a point mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SIN3A-related intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SIN3A-related intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic X-linked intellectual disability Nascimento Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic X-linked intellectual disability Nascimento phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Nonspecific Intellectual Disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Nonspecific Intellectual Disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Uveal coloboma-cleft lip and palate-intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Uveal coloboma-cleft lip and palate-intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
DNHD1-related Intellectual Disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the DNHD1-related Intellectual Disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KIF16B-related Intellectual Disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KIF16B-related Intellectual Disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset parkinsonism-intellectual disability syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset parkinsonism-intellectual disability syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive non-syndromic intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive non-syndromic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked syndromic intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked syndromic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
RLIM-related syndromic intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the RLIM-related syndromic intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Tall stature-intellectual disability-renal anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Tall stature-intellectual disability-renal anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Syndromic X-linked intellectual disability Shashi Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Syndromic X-linked intellectual disability Shashi phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Deafness-intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Deafness-intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Paraplegia-intellectual disability-hyperkeratosis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Paraplegia-intellectual disability-hyperkeratosis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CLIP1-related intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the CLIP1-related intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
RFX3-related intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the RFX3-related intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
SGSM3-related intellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the SGSM3-related intellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal dementia; movement disorders; progressive supranuclear palsy; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease basal ganglia diseases; frontotemporal dementia; progressive supranuclear palsy; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
learning disability Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease learning disability in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
learning disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease learning disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
attention deficit hyperactivity disorder; reading disability Gene Set From GAD Gene-Disease Associations genes associated with the disease attention deficit hyperactivity disorder; reading disability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disability Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term disability in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Relative hand skill in reading disability Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Relative hand skill in reading disability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
learning disability Gene Set From GWASdb SNP-Disease Associations genes associated with the disease learning disability in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
specific learning disability Gene Set From GWASdb SNP-Phenotype Associations genes associated with the specific learning disability phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
specific learning disability Gene Set From HPO Gene-Disease Associations genes associated with the specific learning disability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Specific Learning Disability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Specific Learning Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vision Disability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vision Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Disability Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurological Disability Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurological Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Learning disability Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Learning disability in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Specific learning disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Specific learning disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNQ3-related developmental disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNQ3-related developmental disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
KCNQ3-related Autism and developmental disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the KCNQ3-related Autism and developmental disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Neurodevelopmental Disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Neurodevelopmental Disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
PUM1-associated developmental disability-ataxia-seizure syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the PUM1-associated developmental disability-ataxia-seizure syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
TCF7L2-relatedIntellectual disability Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the TCF7L2-relatedIntellectual disability phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Disability (impaired activities of daily living) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disability (impaired activities of daily living) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Reading disability Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Reading disability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Reading disability or specific language impairment (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Reading disability or specific language impairment (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Reading disability or specific language impairment adjusted for intelligence quotient (pleiotropy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Reading disability or specific language impairment adjusted for intelligence quotient (pleiotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Relative hand skill in reading disability Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Relative hand skill in reading disability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Deafness, cochlear, with myopia and intellectual impairment Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Deafness, cochlear, with myopia and intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
intellectual Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term intellectual in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Profound Intellectual Disabilities Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Profound Intellectual Disabilities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intellectual Developmental Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intellectual Developmental Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Growth Retardation, Intellectual Developmental Disorder, Hypotonia, And Hepatopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal dominant intellectual developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 29 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 29 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 35 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 35 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hyperphosphatasia with impaired intellectual development syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hyperphosphatasia with impaired intellectual development syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive intellectual developmental disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
X-linked intellectual developmental disorder 109 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease X-linked intellectual developmental disorder 109 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 43 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant intellectual developmental disorder 43 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Hyperphosphatasia with impaired intellectual development syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyperphosphatasia with impaired intellectual development syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 35 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 35 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
alacrima, achalasia, and impaired intellectual development syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease alacrima, achalasia, and impaired intellectual development syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyperphosphatasia with impaired intellectual development syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyperphosphatasia with impaired intellectual development syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyperphosphatasia with impaired intellectual development syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyperphosphatasia with impaired intellectual development syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyperphosphatasia with impaired intellectual development syndrome 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyperphosphatasia with impaired intellectual development syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyperphosphatasia with impaired intellectual development syndrome 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyperphosphatasia with impaired intellectual development syndrome 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyperphosphatasia with impaired intellectual development syndrome 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyperphosphatasia with impaired intellectual development syndrome 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Hyperphosphatasia with impaired intellectual development syndrome 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hyperphosphatasia with impaired intellectual development syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 19 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 19 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 56 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 56 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 22 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 22 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 21 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 21 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
blepharophimosis-impaired intellectual development syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease blepharophimosis-impaired intellectual development syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with short stature and behavioral abnormalities Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with short stature and behavioral abnormalities in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked intellectual developmental disorder 108 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked intellectual developmental disorder 108 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with cardiac arrhythmia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with cardiac arrhythmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 38 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 38 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with abnormal behavior, microcephaly, and short stature in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked intellectual developmental disorder 109 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked intellectual developmental disorder 109 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 44 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 44 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 50 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 50 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 23 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 23 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cleft palate, cardiac defects, and intellectual disabillity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cleft palate, cardiac defects, and intellectual disabillity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 29 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 29 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Syndromic X-linked intellectual developmental disorder bain type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Syndromic X-linked intellectual developmental disorder bain type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 36 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 36 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 52 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 52 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 59 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 59 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 51 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 51 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 40 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 40 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 55 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 55 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
non-syndromic X-linked intellectual developmental disorder 111 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease non-syndromic X-linked intellectual developmental disorder 111 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 46 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 46 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 31 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 31 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive intellectual developmental disorder 69 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive intellectual developmental disorder 69 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intellectual developmental disorder with ocular anomalies and distinctive facial features Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Intellectual developmental disorder with ocular anomalies and distinctive facial features in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 54 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 54 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant intellectual developmental disorder 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant intellectual developmental disorder 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Impaired intellectual development and distinctive facial features Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Impaired intellectual development and distinctive facial features phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
INTELLECTUAL DEVELOPMENTAL DISOR Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the INTELLECTUAL DEVELOPMENTAL DISOR phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Blepharophimosis-impaired intellectual development syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Blepharophimosis-impaired intellectual development syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual developmental disorder and retinitis pigmentosa Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual developmental disorder and retinitis pigmentosa phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Intellectual developmental disorder- Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intellectual developmental disorder- phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
USP9X-related intellectual developmental disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the USP9X-related intellectual developmental disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Epilepsy, progressive myoclonic 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Gaze palsy, familial horizontal, with progressive scoliosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Gaze palsy, familial horizontal, with progressive scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Leukoencephalopathy, progressive, with ovarian failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Leukoencephalopathy, progressive, with ovarian failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive pseudorheumatoid dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive pseudorheumatoid dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hyperpigmentation, familial progressive, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hyperpigmentation, familial progressive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial heart block type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial heart block type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Epilepsy, progressive myoclonic 2b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Epilepsy, progressive myoclonic 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive familial intrahepatic cholestasis 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive myoclonus epilepsy with ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive myoclonus epilepsy with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive sclerosing poliodystrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis with progressive nerve deafness Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis with progressive nerve deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Progressive myositis ossificans Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Progressive myositis ossificans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Striatal necrosis, bilateral, and progressive polyneuropathy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Striatal necrosis, bilateral, and progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myoclonic Epilepsies, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myoclonic Epilepsies, Progressive from the curated CTD Gene-Disease Associations dataset.
Cataract, Nuclear Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, Nuclear Progressive from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.
Gaze Palsy, Familial Horizontal, with Progressive Scoliosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gaze Palsy, Familial Horizontal, with Progressive Scoliosis from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 1 from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 2 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 from the curated CTD Gene-Disease Associations dataset.
Gliosis, Familial Progressive Subcortical Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Gliosis, Familial Progressive Subcortical from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS from the curated CTD Gene-Disease Associations dataset.
MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE from the curated CTD Gene-Disease Associations dataset.
Osseous Heteroplasia, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osseous Heteroplasia, Progressive from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Supranuclear Palsy, Progressive, 2 from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Supranuclear Palsy, Progressive, 3 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 from the curated CTD Gene-Disease Associations dataset.
Epilepsy, Progressive Myoclonic, 1b Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Epilepsy, Progressive Myoclonic, 1b from the curated CTD Gene-Disease Associations dataset.
EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease EPILEPSY, PROGRESSIVE MYOCLONIC, 4, WITH OR WITHOUT RENAL FAILURE from the curated CTD Gene-Disease Associations dataset.
Chorioretinal atrophy, progressive bifocal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Chorioretinal atrophy, progressive bifocal from the curated CTD Gene-Disease Associations dataset.
Macrothrombocytopenia progressive deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macrothrombocytopenia progressive deafness from the curated CTD Gene-Disease Associations dataset.
Erythrokeratodermia, Progressive Symmetric Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Erythrokeratodermia, Progressive Symmetric from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness from the curated CTD Gene-Disease Associations dataset.
Progressive hearing loss stapes fixation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive hearing loss stapes fixation from the curated CTD Gene-Disease Associations dataset.
Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Supranuclear Palsy, Progressive from the curated CTD Gene-Disease Associations dataset.
Arthropathy, progressive pseudorheumatoid, of childhood Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthropathy, progressive pseudorheumatoid, of childhood from the curated CTD Gene-Disease Associations dataset.
Leukoencephalopathy, Progressive Multifocal Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Leukoencephalopathy, Progressive Multifocal from the curated CTD Gene-Disease Associations dataset.
Progressive Familial Heart Block, Type Ib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive Familial Heart Block, Type Ib from the curated CTD Gene-Disease Associations dataset.
Cholestasis, progressive familial intrahepatic 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cholestasis, progressive familial intrahepatic 3 from the curated CTD Gene-Disease Associations dataset.
Bulbar Palsy, Progressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Bulbar Palsy, Progressive from the curated CTD Gene-Disease Associations dataset.
Ophthalmoplegia, Chronic Progressive External Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ophthalmoplegia, Chronic Progressive External from the curated CTD Gene-Disease Associations dataset.
Nephropathy, Progressive, with Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nephropathy, Progressive, with Deafness from the curated CTD Gene-Disease Associations dataset.
Progressive supranuclear palsy atypical Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive supranuclear palsy atypical from the curated CTD Gene-Disease Associations dataset.
Renal Failure, Progressive, with Hypertension Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Failure, Progressive, with Hypertension from the curated CTD Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 from the curated CTD Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Supranuclear Palsy, Progressive in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
chronic progressive external ophthalmoplegia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease chronic progressive external ophthalmoplegia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
progressive myoclonus epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease progressive myoclonus epilepsy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
progressive supranuclear palsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease progressive supranuclear palsy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
progressive supranuclear palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive supranuclear palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive bulbar palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive bulbar palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
chronic progressive external ophthalmoplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease chronic progressive external ophthalmoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive multifocal leukoencephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive multifocal leukoencephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
rapidly progressive glomerulonephritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease rapidly progressive glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
progressive myoclonus epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease progressive myoclonus epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
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.
slowly progressive als Gene Set From GAD Gene-Disease Associations genes associated with the disease slowly progressive als in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial atypical progressive supranuclear palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease familial atypical progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia, primary progressive; dementia Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia, primary progressive; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease machado-joseph disease; myoclonic epilepsies, progressive; myotonic dystrophy; oligospermia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ophthalmoplegia, chronic progressive external Gene Set From GAD Gene-Disease Associations genes associated with the disease ophthalmoplegia, chronic progressive external in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
primary progressive aphasia Gene Set From GAD Gene-Disease Associations genes associated with the disease primary progressive aphasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive supranuclear palsy Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive supranuclear palsy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neurodegenerative diseases; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dominant progressive deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease dominant progressive deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
aphasia, primary progressive; heredodegenerative disorders, nervous system Gene Set From GAD Gene-Disease Associations genes associated with the disease aphasia, primary progressive; heredodegenerative disorders, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
rapidly progressive familial amyotrophic lateral sclerosis Gene Set From GAD Gene-Disease Associations genes associated with the disease rapidly progressive familial amyotrophic lateral sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain diseases; neurodegenerative diseases; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease brain diseases; neurodegenerative diseases; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive av-block and anomalous venous return Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive av-block and anomalous venous return in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive external ophthalmoplegia Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive external ophthalmoplegia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multiple sclerosis, chronic progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease multiple sclerosis, chronic progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
als/amyotrophic lateral sclerosis; progressive muscular atrophy Gene Set From GAD Gene-Disease Associations genes associated with the disease als/amyotrophic lateral sclerosis; progressive muscular atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; huntington disease Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; huntington disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dementia; supranuclear palsy, progressive Gene Set From GAD Gene-Disease Associations genes associated with the disease dementia; supranuclear palsy, progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive renal damage Gene Set From GAD Gene-Disease Associations genes associated with the disease progressive renal damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome inversion; dementia; supranuclear palsy, progressive; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; huntington disease; insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; huntington disease; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chronic progressive chorea; memory disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease chronic progressive chorea; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
progressive Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term progressive in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
progressive supranuclear palsy Gene Set From GWASdb SNP-Disease Associations genes associated with the disease progressive supranuclear palsy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
progressive cataract Gene Set From HPO Gene-Disease Associations genes associated with the progressive cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive inability to walk Gene Set From HPO Gene-Disease Associations genes associated with the progressive inability to walk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive congenital scoliosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive congenital scoliosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive visual field defects Gene Set From HPO Gene-Disease Associations genes associated with the progressive visual field defects phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symmetrical progressive peripheral demyelination Gene Set From HPO Gene-Disease Associations genes associated with the symmetrical progressive peripheral demyelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive spastic paraplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive spastic paraplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cone degeneration Gene Set From HPO Gene-Disease Associations genes associated with the progressive cone degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive vitiligo Gene Set From HPO Gene-Disease Associations genes associated with the progressive vitiligo phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive neurologic deterioration Gene Set From HPO Gene-Disease Associations genes associated with the progressive neurologic deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive spastic quadriplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive spastic quadriplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive psychomotor deterioration Gene Set From HPO Gene-Disease Associations genes associated with the progressive psychomotor deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive reticulate hyperpigmentation Gene Set From HPO Gene-Disease Associations genes associated with the progressive reticulate hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive fusion 2nd-5th pip joints Gene Set From HPO Gene-Disease Associations genes associated with the progressive fusion 2nd-5th pip joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive encephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive encephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive extrapyramidal movement disorder Gene Set From HPO Gene-Disease Associations genes associated with the progressive extrapyramidal movement disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive gait ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive gait ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive inspiratory stridor Gene Set From HPO Gene-Disease Associations genes associated with the progressive inspiratory stridor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive choreoathetosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive choreoathetosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive spasticity Gene Set From HPO Gene-Disease Associations genes associated with the progressive spasticity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive peripheral neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive peripheral neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive sclerosis of skull base Gene Set From HPO Gene-Disease Associations genes associated with the progressive sclerosis of skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive clavicular acroosteolysis Gene Set From HPO Gene-Disease Associations genes associated with the progressive clavicular acroosteolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive alopecia Gene Set From HPO Gene-Disease Associations genes associated with the progressive alopecia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive truncal ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive truncal ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
subacute progressive viral hepatitis Gene Set From HPO Gene-Disease Associations genes associated with the subacute progressive viral hepatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive central visual loss Gene Set From HPO Gene-Disease Associations genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive language deterioration Gene Set From HPO Gene-Disease Associations genes associated with the progressive language deterioration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive hyperpigmentation Gene Set From HPO Gene-Disease Associations genes associated with the progressive hyperpigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive hypotrichosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive hypotrichosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive sensorineural hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive pulmonary function impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive pulmonary function impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive forgetfulness Gene Set From HPO Gene-Disease Associations genes associated with the progressive forgetfulness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive microcephaly Gene Set From HPO Gene-Disease Associations genes associated with the progressive microcephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive alveolar ridge hypertropy Gene Set From HPO Gene-Disease Associations genes associated with the progressive alveolar ridge hypertropy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive proximal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive macrocephaly Gene Set From HPO Gene-Disease Associations genes associated with the progressive macrocephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive external ophthalmoplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive external ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive night blindness Gene Set From HPO Gene-Disease Associations genes associated with the progressive night blindness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive macular scarring Gene Set From HPO Gene-Disease Associations genes associated with the progressive macular scarring phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive ptosis Gene Set From HPO Gene-Disease Associations genes associated with the progressive ptosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive calcification of costochondral cartilage Gene Set From HPO Gene-Disease Associations genes associated with the progressive calcification of costochondral cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cervical vertebral spine fusion Gene Set From HPO Gene-Disease Associations genes associated with the progressive cervical vertebral spine fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive conductive hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the progressive conductive hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
rapidly progressive Gene Set From HPO Gene-Disease Associations genes associated with the rapidly progressive phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive leukoencephalopathy Gene Set From HPO Gene-Disease Associations genes associated with the progressive leukoencephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the progressive retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive flexion contractures Gene Set From HPO Gene-Disease Associations genes associated with the progressive flexion contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive visual loss Gene Set From HPO Gene-Disease Associations genes associated with the progressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive disorder Gene Set From HPO Gene-Disease Associations genes associated with the progressive disorder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive ophthalmoplegia Gene Set From HPO Gene-Disease Associations genes associated with the progressive ophthalmoplegia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cerebellar ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive cerebellar ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Multiple Sclerosis, Chronic Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Sclerosis, Chronic Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myoclonic Epilepsies, Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myoclonic Epilepsies, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Bulbar Palsy, Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Bulbar Palsy, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Supranuclear Palsy, Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Supranuclear Palsy, Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Aphasia, Primary Progressive Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Aphasia, Primary Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Ophthalmoplegia, Chronic Progressive External Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ophthalmoplegia, Chronic Progressive External phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Progressive rod-cone degeneration protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Progressive rod-cone degeneration protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Progressive ankylosis Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Progressive ankylosis protein domain from the InterPro Predicted Protein Domain Annotations dataset.
progressive muscle weakness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
progressive hair loss Gene Set From MPO Gene-Phenotype Associations gene mutations causing the progressive hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
deafness, x-linked 1, progressive Gene Set From OMIM Gene-Disease Associations genes associated with the deafness, x-linked 1, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 3, with or without intracellular inclusions Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 3, with or without intracellular inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive canalicular Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive canalicular phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 2b (lafora) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 2b (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal dominant, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal dominant, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive familial heart block, type ib Gene Set From OMIM Gene-Disease Associations genes associated with the progressive familial heart block, type ib phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.
macrothrombocytopenia and progressive sensorineural deafness Gene Set From OMIM Gene-Disease Associations genes associated with the macrothrombocytopenia and progressive sensorineural deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy with progressive myoclonic epilepsy phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive atypical Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive atypical phenotype from the curated OMIM Gene-Disease Associations dataset.
thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene Set From OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
supranuclear palsy, progressive Gene Set From OMIM Gene-Disease Associations genes associated with the supranuclear palsy, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
hyperpigmentation, familial progressive, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the hyperpigmentation, familial progressive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
cholestasis, progressive familial intrahepatic 4 Gene Set From OMIM Gene-Disease Associations genes associated with the cholestasis, progressive familial intrahepatic 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
aphasia, primary progressive Gene Set From OMIM Gene-Disease Associations genes associated with the aphasia, primary progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
spondyloepiphyseal dysplasia tarda with progressive arthropathy Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepiphyseal dysplasia tarda with progressive arthropathy phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene Set From OMIM Gene-Disease Associations genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 6 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 5 Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
cone dystrophy, progressive x-linked, 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cone dystrophy, progressive x-linked, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
leukoencephalopathy, progressive, with ovarian failure Gene Set From OMIM Gene-Disease Associations genes associated with the leukoencephalopathy, progressive, with ovarian failure phenotype from the curated OMIM Gene-Disease Associations dataset.
osseous heteroplasia, progressive Gene Set From OMIM Gene-Disease Associations genes associated with the osseous heteroplasia, progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 4, with or without renal failure Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 4, with or without renal failure phenotype from the curated OMIM Gene-Disease Associations dataset.
nephropathy, progressive, with deafness Gene Set From OMIM Gene-Disease Associations genes associated with the nephropathy, progressive, with deafness phenotype from the curated OMIM Gene-Disease Associations dataset.
gaze palsy, horizontal, with progressive scoliosis Gene Set From OMIM Gene-Disease Associations genes associated with the gaze palsy, horizontal, with progressive scoliosis phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
arthropathy, progressive pseudorheumatoid, of childhood Gene Set From OMIM Gene-Disease Associations genes associated with the arthropathy, progressive pseudorheumatoid, of childhood phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia with mitochondrial dna deletions 3 Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia with mitochondrial dna deletions 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
encephalopathy, progressive, with or without lipodystrophy Gene Set From OMIM Gene-Disease Associations genes associated with the encephalopathy, progressive, with or without lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
cataract 27, nuclear progressive Gene Set From OMIM Gene-Disease Associations genes associated with the cataract 27, nuclear progressive phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
progressive external ophthalmoplegia, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the progressive external ophthalmoplegia, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
heart block, progressive, type ia Gene Set From OMIM Gene-Disease Associations genes associated with the heart block, progressive, type ia phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 1a (unverricht and lundborg) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 1a (unverricht and lundborg) phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 1b Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
epilepsy, progressive myoclonic 2a (lafora) Gene Set From OMIM Gene-Disease Associations genes associated with the epilepsy, progressive myoclonic 2a (lafora) phenotype from the curated OMIM Gene-Disease Associations dataset.
Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 Gene Set From Reactome Pathways 2014 proteins participating in the Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 pathway from the Reactome Pathways dataset.
Primary Progressive Aphasia (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Progressive Aphasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone Dystrophy (Without Rod Involvement) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy (Without Rod Involvement) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cgvhd Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cgvhd in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Intrahepatic Cholestasis (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Intrahepatic Cholestasis (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Rapidly Progressive Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Rapidly Progressive Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Slowly Progressive Insulin Dependent Diabetes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Slowly Progressive Insulin Dependent Diabetes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Glomerulonephritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Glomerulonephritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Supranuclear Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Supranuclear Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Pseudorheumatoid Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Pseudorheumatoid Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Sensorineural Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Sensorineural Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
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.
Multiple Sclerosis, Primary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Primary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Progressive External Ophthalmoplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Progressive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Progressive Myoclonic Epilepsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Myoclonic Epilepsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cerebellar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone-Rod Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone-Rod Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary Progressive Nonfluent Aphasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Primary Progressive Nonfluent Aphasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Multiple Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Distal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Post Hemorrhagic Ventricular Dilatation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Post Hemorrhagic Ventricular Dilatation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cataract Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Dementia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Dementia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chronic Progressive Chorea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chronic Progressive Chorea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Bulbar Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Bulbar Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive 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.
Multiple Sclerosis, Secondary Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Secondary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Sclerosis, Chronic Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Sclerosis, Chronic Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Periodontitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Periodontitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Ptosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Ptosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Brain Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Brain Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cone Dystrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cone Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive External Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Ophthalmoplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Ophthalmoplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cardiomyopathic Lentiginosis Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cardiomyopathic Lentiginosis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Non-Small Cell Lung Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Non-Small Cell Lung Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ophthalmoplegia, Progressive Supranuclear Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ophthalmoplegia, Progressive Supranuclear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Supranuclear Palsy, Progressive, 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Atrophy, Progressive Bifocal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Atrophy, Progressive Bifocal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Renal Failure, Progressive, With Hypertension Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Renal Failure, Progressive, With Hypertension in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pf-Ild-Progressive Fibrosing Interstitial Lung Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pf-Ild-Progressive Fibrosing Interstitial Lung Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Logopenic Progressive Aphasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Logopenic Progressive Aphasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Encephalomyelitis With Rigidity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Encephalomyelitis With Rigidity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symmetrical Progressive Peripheral Demyelination Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symmetrical Progressive Peripheral Demyelination in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Hearing Loss Stapes Fixation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Hearing Loss Stapes Fixation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Chorea Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Chorea in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Non-Progressive Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Non-Progressive Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prickle1-Related Progressive Myoclonus Epilepsy With Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prickle1-Related Progressive Myoclonus Epilepsy With Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Piebaldism, Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Piebaldism, Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Familial Progressive Hyper And Hypopigmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Familial Progressive Hyper And Hypopigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Reticulate Hyperpigmentation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Reticulate Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Subcortical Gliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Subcortical Gliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Supranuclear Palsy, Progressive, 1, Atypical Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Supranuclear Palsy, Progressive, 1, Atypical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Visual Impairment And Progressive Phthisis Bulbi Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Visual Impairment And Progressive Phthisis Bulbi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macrothrombocytopenia And Progressive Sensorineural Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macrothrombocytopenia And Progressive Sensorineural Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cavitating Leukoencephalopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cavitating Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rapidly Progressive Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rapidly Progressive Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Optic Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysphagia, Progressive Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysphagia, Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Congenital Scoliosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Congenital Scoliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Polyneuropathy With Bilateral Striatal Necrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Polyneuropathy With Bilateral Striatal Necrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Progressive Bulbar Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Progressive Bulbar Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Proximal Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Proximal Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Myoclonic Epilepsy With Dystonia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Myoclonic Epilepsy With Dystonia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Familial Heart Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Familial Heart Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Leukoencephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Peripheral Neuropathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Peripheral Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Night Blindness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Night Blindness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Neoplastic Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Neoplastic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Neurologic Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Neurologic Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Paraplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spasticity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Proximal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Microcephaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Quadriplegia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Quadriplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Cervical Vertebral Spine Fusion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Cervical Vertebral Spine Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Spastic Paraparesis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Spastic Paraparesis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Visual Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Flexion Contractures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Flexion Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Macrocephaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Macrocephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Gait Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Gait Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Inability To Walk Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Inability To Walk in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Pes Cavus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Pes Cavus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Subacute Progressive Viral Hepatitis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subacute Progressive Viral Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Rapidly Progressive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Rapidly Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Psychomotor Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Psychomotor Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Paraparesis, Chronic Progressive Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Paraparesis, Chronic Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Extrapyramidal Movement Disorder Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Extrapyramidal Movement Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Intervertebral Space Narrowing Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Intervertebral Space Narrowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Clavicular Acroosteolysis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Clavicular Acroosteolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Conductive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Conductive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Visual Field Defects Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Visual Field Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Encephalopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Encephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Distal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sensorineural Hearing Loss, Progressive Bilateral Postlingual Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sensorineural Hearing Loss, Progressive Bilateral Postlingual in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Ventriculomegaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Language Deterioration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Language Deterioration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Calcification Of Costochondral Cartilage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Calcification Of Costochondral Cartilage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Alveolar Ridge Hypertropy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Alveolar Ridge Hypertropy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Forgetfulness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Forgetfulness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Truncal Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Truncal Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Hyperpigmentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Hyperpigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Choreoathetosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Choreoathetosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Loss Of Facial Adipose Tissue Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Loss Of Facial Adipose Tissue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Extrapyramidal Muscular Rigidity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Extrapyramidal Muscular Rigidity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Leg Bowing Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Leg Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Vitiligo Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Vitiligo in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Hypotrichosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Hypotrichosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Pulmonary Function Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Pulmonary Function Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Fusion 2Nd-5Th Pip Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Fusion 2Nd-5Th Pip Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Sclerosis Of Skull Base Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Sclerosis Of Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adult-Onset Chronic Progressive External Ophthalmoplegia With Mitochondrial Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Inspiratory Stridor Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Inspiratory Stridor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Alopecia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Alopecia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
progressive muscle weakness Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased sperm progressive motility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased sperm progressive motility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
progressive hair loss Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal sperm progressive motility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sperm progressive motility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 Gene Set From Reactome Pathways 2024 proteins participating in the Progressive trimming of alpha-1,2-linked mannose residues from Man9/8/7GlcNAc2 to produce Man5GlcNAc2 pathway from the Reactome Pathways 2024 dataset.
Chronic progressive external ophthalmoplegia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chronic progressive external ophthalmoplegia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive familial heart block Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive familial heart block from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive bulbar palsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive bulbar palsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive familial intrahepatic cholestasis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive supranuclear palsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive supranuclear palsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1B Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 1B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1A Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 1A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spinal muscular atrophy with progressive myoclonic epilepsy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive osseous heteroplasia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive osseous heteroplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 4 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive myoclonus epilepsy 4 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive pseudorheumatoid arthropathy of childhood Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Progressive pseudorheumatoid arthropathy of childhood from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Progressive bulbar palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive bulbar palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive supranuclear palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive supranuclear palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary progressive multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Secondary progressive multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Secondary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial intrahepatic cholestasis 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial intrahepatic cholestasis 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chronic progressive external ophthalmoplegia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chronic progressive external ophthalmoplegia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Primary progressive aphasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary progressive aphasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spastic tetraplegia, thin corpus callosum, and progressive microcephaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spastic tetraplegia, thin corpus callosum, and progressive microcephaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive non-fluent aphasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive non-fluent aphasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive leukoencephalopathy with ovarian failure Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive leukoencephalopathy with ovarian failure in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive multifocal leukoencephalopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive multifocal leukoencephalopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Rapidly progressive glomerulonephritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Rapidly progressive glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive relapsing multiple sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive relapsing multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spinal muscular atrophy with progressive myoclonic epilepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spinal muscular atrophy with progressive myoclonic epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Logopenic progressive aphasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Logopenic progressive aphasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type IA Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type IA in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive osseous heteroplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive osseous heteroplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type II Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type II in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive familial heart block type IB Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive familial heart block type IB in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial progressive hyperpigmentation with or without hypopigmentation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial progressive hyperpigmentation with or without hypopigmentation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Early onset progressive encephalopathy with brain atrophy and thin corpus callosum Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Early onset progressive encephalopathy with brain atrophy and thin corpus callosum in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive pseudorheumatoid arthropathy of childhood Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive pseudorheumatoid arthropathy of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Idiopathic progressive polyneuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Idiopathic progressive polyneuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonus epilepsy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Progressive myoclonus epilepsy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Visual impairment and progressive phthisis bulbi in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Progressive myoclonic epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive myoclonic epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive distal muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive proximal muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sclerosing poliodystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sclerosing poliodystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive pseudorheumatoid dysplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive pseudorheumatoid dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive familial intrahepatic cholestasis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive familial intrahepatic cholestasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive cone dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive cone dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive familial heart block Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive familial heart block phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive supranuclear palsy-parkinsonism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive supranuclear palsy-parkinsonism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive supranuclear ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive supranuclear ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive osseous heteroplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive osseous heteroplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive sensorineural hearing impairment Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive sensorineural hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive scapulohumeroperoneal distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive scapulohumeroperoneal distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive myositis ossificans Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive myositis ossificans phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spinal muscular atrophy-progressive myoclonic epilepsy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spinal muscular atrophy-progressive myoclonic epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked progressive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked progressive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive microcephaly-seizures-cortical blindness-developmental delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Chronic and progressive ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Chronic and progressive ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-progressive congenital cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-progressive congenital cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary progressive aphasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary progressive aphasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Skeletal dysplasia and progressive central nervous system degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal dysplasia and progressive central nervous system degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive demyelinating neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive demyelinating neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive neurologic deterioration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive neurologic deterioration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive bulbar palsy of childhood Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive bulbar palsy of childhood phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Primary progressive multiple sclerosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary progressive multiple sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive spasticity Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive spasticity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive childhood encephalopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive childhood encephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive microcephaly Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive peripheral neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive peripheral neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive gait ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive gait ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive retinal dystrophy due to retinol transport defect Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive retinal dystrophy due to retinol transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive muscular dystrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Visual impairment and progressive phthisis bulbi Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Visual impairment and progressive phthisis bulbi phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

intellectual disability, progressive Gene Set

Intellectual Disability, Progressive Gene Set

Severe Intellectual Disability And Progressive Spastic Paraplegia Gene Set

Severe intellectual disability-progressive spastic diplegia syndrome Gene Set

Progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome Gene Set

Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome Gene Set

Blepharophimosis-ptosis-intellectual disability syndrome Gene Set

Coffin Siris/Intellectual Disability Gene Set

Syndromic intellectual disability Gene Set

Intellectual Disability Gene Set

syndromic intellectual disability Gene Set

intellectual disability Gene Set

intellectual disability Gene Set

syndromic intellectual disability Gene Set

non-syndromic intellectual disability Gene Set

intellectual disability, moderate Gene Set

intellectual disability, severe Gene Set

intellectual disability, profound Gene Set

intellectual disability, mild Gene Set

intellectual disability Gene Set

Intellectual Disability Gene Set

blepharophimosis-ptosis-intellectual disability syndrome Gene Set

Severe Intellectual Disability Gene Set

Moderate Intellectual Disability Gene Set

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

Borderline Intellectual Disability Gene Set

Ahdc1-Related Intellectual Disability, Obstructive Sleep Apnea, Mild Dysmorphism Syndrome Gene Set

Hivep2-Related Intellectual Disability Gene Set

Early-Onset Epileptic Encephalopathy And Intellectual Disability Due To Grin2A Mutation Gene Set

Intellectual Disability Gene Set

Intellectual disability Gene Set

X-linked intellectual disability-psychosis-macroorchidism syndrome Gene Set

Syndromic X-linked intellectual disability Gene Set

Syndromic X-linked intellectual disability Lubs type Gene Set

Syndromic intellectual disability Gene Set

Syndromic X-linked intellectual disability Snyder type Gene Set

Syndromic X-linked intellectual disability Siderius type Gene Set

Alpha thalassemia-X-linked intellectual disability syndrome Gene Set

Intellectual disability Gene Set

non-syndromic intellectual disability Gene Set

Syndromic X-linked intellectual disability 5 Gene Set

Syndromic X-linked intellectual disability Gene Set

Syndromic intellectual disability Gene Set

Syndromic X-linked intellectual disability 94 Gene Set

non-syndromic X-linked intellectual disability 99 Gene Set

Syndromic X-linked intellectual disability Shashi type Gene Set

Intellectual disability-severe speech delay-mild dysmorphism syndrome Gene Set

Alpha thalassemia-intellectual disability syndrome type 1 Gene Set

Syndromic X-linked intellectual disability Cabezas type Gene Set

Syndromic X-linked intellectual disability Pilorge type Gene Set

Syndromic X-linked intellectual disability Lubs type Gene Set

non-syndromic X-linked intellectual disability Gene Set

X-linked intellectual disability-psychosis-macroorchidism syndrome Gene Set

Stocco Dos Santos type X-linked intellectual disability Gene Set

non-syndromic X-linked intellectual disability 98 Gene Set

non-syndromic X-linked intellectual disability 91 Gene Set

non-syndromic X-linked intellectual disability 58 Gene Set

deafness-intellectual disability, Martin-Probst type syndrome Gene Set

Syndromic X-linked intellectual disability Claes-Jensen type Gene Set

Syndromic X-linked intellectual disability type 10 Gene Set

Syndromic X-linked intellectual disability Najm type Gene Set

Syndromic X-linked intellectual disability Snyder type Gene Set

Syndromic X-linked intellectual disability Turner type Gene Set

Alpha thalassemia-X-linked intellectual disability syndrome Gene Set

Syndromic X-linked intellectual disability Siderius type Gene Set

non-syndromic X-linked intellectual disability 81 Gene Set

non-syndromic X-linked intellectual disability 63 Gene Set

Uveal coloboma-cleft lip and palate-intellectual disability Gene Set

non-syndromic X-linked intellectual disability 106 Gene Set

non-syndromic X-linked intellectual disability 30 Gene Set

non-syndromic X-linked intellectual disability 101 Gene Set

non-syndromic X-linked intellectual disability 103 Gene Set

non-syndromic X-linked intellectual disability 1 Gene Set

non-syndromic X-linked intellectual disability 90 Gene Set

Congenital muscular dystrophy with cataracts and intellectual disability Gene Set

female-restricted syndromic X-linked intellectual disability 99 Gene Set

Syndromic X-linked intellectual disability Raymond type Gene Set

non-syndromic X-linked intellectual disability 21 Gene Set

X-linked intellectual disability-short stature-overweight syndrome Gene Set