Intellectual disability, mild

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Results for "Intellectual disability, mild": 412 gene sets

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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.
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.
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.
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.
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.
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.
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, 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, 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 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.
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.
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.
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.
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.
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.
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-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.
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.
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.
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.
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.
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.
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.
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.
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Metachromatic leukodystrophy, mild Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Metachromatic leukodystrophy, mild phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Sensorineural deafness with mild renal dysfunction Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Sensorineural deafness with mild renal dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MUCOPOLYSACCHARIDOSIS, TYPE VI, MILD Gene Set From ClinVar Gene-Phenotype Associations genes associated with the MUCOPOLYSACCHARIDOSIS, TYPE VI, MILD phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
MONONEUROPATHY OF THE MEDIAN NERVE, MILD Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease MONONEUROPATHY OF THE MEDIAN NERVE, MILD from the curated CTD Gene-Disease Associations dataset.
Osteoarthritis with Mild Chondrodysplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteoarthritis with Mild Chondrodysplasia from the curated CTD Gene-Disease Associations dataset.
Mild Cognitive Impairment Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mild Cognitive Impairment from the curated CTD Gene-Disease Associations dataset.
mild pre-eclampsia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mild pre-eclampsia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
mild chondrodysplasia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild chondrodysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild cognitive impairment Gene Set From GAD Gene-Disease Associations genes associated with the disease mild cognitive impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild phenotype xeroderma pigmentosum Gene Set From GAD Gene-Disease Associations genes associated with the disease mild phenotype xeroderma pigmentosum in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild osteogenesis imperfecta Gene Set From GAD Gene-Disease Associations genes associated with the disease mild osteogenesis imperfecta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild familial hypercholesterolaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild familial hypercholesterolaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild and severe substance abuse Gene Set From GAD Gene-Disease Associations genes associated with the disease mild and severe substance abuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild hyperhomocysteinaemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild hyperhomocysteinaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild myotubular myopathy Gene Set From GAD Gene-Disease Associations genes associated with the disease mild myotubular myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild hdn Gene Set From GAD Gene-Disease Associations genes associated with the disease mild hdn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild ehlers-danlos syndrome type iv Gene Set From GAD Gene-Disease Associations genes associated with the disease mild ehlers-danlos syndrome type iv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild dyslipidemia Gene Set From GAD Gene-Disease Associations genes associated with the disease mild dyslipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild gestational diabetes mellitus Gene Set From GAD Gene-Disease Associations genes associated with the disease mild gestational diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild homocystinuria Gene Set From GAD Gene-Disease Associations genes associated with the disease mild homocystinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mild Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term mild in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
mild postnatal growth retardation Gene Set From HPO Gene-Disease Associations genes associated with the mild postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild global developmental delay Gene Set From HPO Gene-Disease Associations genes associated with the mild global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the mild hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild neurosensory hearing impairment Gene Set From HPO Gene-Disease Associations genes associated with the mild neurosensory hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild intrauterine growth retardation Gene Set From HPO Gene-Disease Associations genes associated with the mild intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild short stature Gene Set From HPO Gene-Disease Associations genes associated with the mild short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mild proteinuria Gene Set From HPO Gene-Disease Associations genes associated with the mild proteinuria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
maple syrup urine disease, mild variant Gene Set From OMIM Gene-Disease Associations genes associated with the maple syrup urine disease, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.
brachyolmia 4 with mild epiphyseal and metaphyseal changes Gene Set From OMIM Gene-Disease Associations genes associated with the brachyolmia 4 with mild epiphyseal and metaphyseal changes phenotype from the curated OMIM Gene-Disease Associations dataset.
obesity, mild, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the obesity, mild, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
{malaria, mild, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {malaria, mild, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant phenotype from the curated OMIM Gene-Disease Associations dataset.
mononeuropathy of the median nerve, mild Gene Set From OMIM Gene-Disease Associations genes associated with the mononeuropathy of the median nerve, mild phenotype from the curated OMIM Gene-Disease Associations dataset.
osteoarthritis with mild chondrodysplasia Gene Set From OMIM Gene-Disease Associations genes associated with the osteoarthritis with mild chondrodysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
[hyperphenylalaninemia, non-pku mild] Gene Set From OMIM Gene-Disease Associations genes associated with the [hyperphenylalaninemia, non-pku mild] phenotype from the curated OMIM Gene-Disease Associations dataset.
arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair Gene Set From OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.
sensorineural deafness with mild renal dysfunction Gene Set From OMIM Gene-Disease Associations genes associated with the sensorineural deafness with mild renal dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset.
Mild Mental Retardation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Mental Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Cognitive Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Cognitive Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Expressive Language Delay Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Expressive Language Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Bronchopulmonary Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Bronchopulmonary Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Dementia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Dementia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Non-Proliferative Diabetic Retinopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Non-Proliferative Diabetic Retinopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Neurosensory Hearing Impairment Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Neurosensory Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Persistent Asthma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Persistent Asthma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Hereditary Factor Viii Deficiency Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Hereditary Factor Viii Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Maroteaux-Lamy Syndrome, Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Maroteaux-Lamy Syndrome, Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Citrullinemia, Mild Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Citrullinemia, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Mood Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Mood Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bjornstad Syndrome With Mild Mitochondrial Complex Iii Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bjornstad Syndrome With Mild Mitochondrial Complex Iii Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Sensorineural Deafness With Mild Renal Dysfunction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Sensorineural Deafness With Mild Renal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Encephalitis/Encephalopathy, Mild, With Reversible Myelin Vacuolization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Steroid 21-Hydroxylase Deficiency Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Steroid 21-Hydroxylase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Idiopathic Infantile Hypercalcemia - Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Idiopathic Infantile Hypercalcemia - Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Depression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Depression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Fetal Ventriculomegaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Fetal Ventriculomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hunter'S Syndrome, Mild Form Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hunter'S Syndrome, Mild Form in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mcardle Disease, Mild Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mcardle Disease, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Hypermetropia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mild Hypermetropia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mononeuropathy Of The Median Nerve, Mild Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mononeuropathy Of The Median Nerve, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mild Global Developmental Delay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Global Developmental Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Postnatal Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Postnatal Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Short Stature Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Short Stature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Canavan Disease, Mild Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Canavan Disease, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Proteinuria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Proteinuria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Conductive Hearing Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Conductive Hearing Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Microcephaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Intrauterine Growth Retardation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Intrauterine Growth Retardation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Eczema Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Eczema in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Dysmorphic Features Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Dysmorphic Features in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Myopia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Myopia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Apparent Mineralocorticoid Excess, Mild Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Apparent Mineralocorticoid Excess, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Developmental Delay, Mild Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Developmental Delay, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Facial Dysmorphism, Mild Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Dysmorphism, Mild in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Adverse Event Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Adverse Event in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Thrombocytopenia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Thrombocytopenia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Splenomegaly Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Splenomegaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mild Radial Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mild Radial Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
H139Hfs13* PPM1K causes a mild variant of MSUD Gene Set From Reactome Pathways 2024 proteins participating in the H139Hfs13* PPM1K causes a mild variant of MSUD pathway from the Reactome Pathways 2024 dataset.
Mild cognitive impairment Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mild cognitive impairment in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mild pre-eclampsia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mild pre-eclampsia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Persistent mild asthma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Persistent mild asthma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Mild non-PKU hyperphenylalanemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild non-PKU hyperphenylalanemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mild hyperphenylalaninemia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild hyperphenylalaninemia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mild Canavan disease Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild Canavan disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mild hemophilia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild hemophilia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mild proteinuria Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild proteinuria phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mild macrothrombocytopenia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mild macrothrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
CV-A6-associated hand, foot, and mouth disease (severe vs mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the CV-A6-associated hand, foot, and mouth disease (severe vs mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mild influenza (H1N1) infection Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mild influenza (H1N1) infection phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cognitive decline rate in late mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cognitive decline rate in late mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Rate of cognitive decline in mild cognitive impairment (time interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Rate of cognitive decline in mild cognitive impairment (time interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HIV-associated neurocognitive disorder (mild neurocognitive disorder or asymptomatic neurocognitive impairment) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIV-associated neurocognitive disorder (mild neurocognitive disorder or asymptomatic neurocognitive impairment) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
HIV-associated neurocognitive disorder (mild neurocognitive disorder) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the HIV-associated neurocognitive disorder (mild neurocognitive disorder) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hematuria (mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hematuria (mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Glucosuria (mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glucosuria (mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Proteinuria (mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Proteinuria (mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ketonuria (mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ketonuria (mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Erosive tooth wear (severe vs none or mild) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erosive tooth wear (severe vs none or mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mild to moderate chronic kidney disease Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mild to moderate chronic kidney disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hippocampal volume in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hippocampal volume in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Logical memory (immediate recall) in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Logical memory (immediate recall) in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Logical memory (delayed recall) in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Logical memory (delayed recall) in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cerebrospinal AB1-42 levels in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebrospinal AB1-42 levels in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cerebrospinal fluid t-tau levels in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebrospinal fluid t-tau levels in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Cerebrospinal fluid p-tau levels in mild cognitive impairment Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cerebrospinal fluid p-tau levels in mild cognitive impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Accelerated cognitive decline after conversion of mild cognitive impairment to Alzheimer's disease (Alzhiemer's diagnosis trajectory interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Accelerated cognitive decline after conversion of mild cognitive impairment to Alzheimer's disease (Alzhiemer's diagnosis trajectory interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Recurrence of malaria infection (mild or asymptomatic) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrence of malaria infection (mild or asymptomatic) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Recurrence of mild malaria attacks Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Recurrence of mild malaria attacks phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mild obesity-related type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mild obesity-related type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mild age-related type 2 diabetes Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mild age-related type 2 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 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.

Harmonizome 3.0

intellectual disability, mild Gene Set

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

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

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

AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome Gene Set

Micrognathia-recurrent infections-behavioral abnormalities-mild 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, progressive Gene Set

intellectual disability, profound 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

Severe Intellectual Disability And Progressive Spastic Paraplegia Gene Set

Hivep2-Related Intellectual Disability Gene Set

Intellectual Disability, Progressive 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

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