| Name |
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fragility Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term fragility in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bone fragility with contractures, arterial rupture, and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bone fragility with contractures, arterial rupture, and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin fragility woolly hair syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin fragility woolly hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ectodermal dysplasia skin fragility syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ectodermal dysplasia skin fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin Fragility-Woolly Hair Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Skin Fragility-Woolly Hair Syndrome from the curated CTD Gene-Disease Associations dataset. |
Ectodermal dysplasia/ skin fragility syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ectodermal dysplasia/ skin fragility syndrome from the curated CTD Gene-Disease Associations dataset. |
Bone Fragility with Contractures, Arterial Rupture, and Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bone Fragility with Contractures, Arterial Rupture, and Deafness from the curated CTD Gene-Disease Associations dataset. |
increased red cell osmotic fragility Gene SetFrom HPO Gene-Disease Associations genes associated with the increased red cell osmotic fragility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
skin fragility with non-scarring blistering Gene SetFrom HPO Gene-Disease Associations genes associated with the skin fragility with non-scarring blistering phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature delivery because of cervical insufficiency or membrane fragility Gene SetFrom HPO Gene-Disease Associations genes associated with the premature delivery because of cervical insufficiency or membrane fragility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Chromosome Fragility Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Fragility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
ectodermal dysplasia/skin fragility syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia/skin fragility syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
skin fragility-woolly hair syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the skin fragility-woolly hair syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
Skin Fragility-Woolly Hair Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Skin Fragility-Woolly Hair Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hereditary Vascular Fragility Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hereditary Vascular Fragility in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bone Fragility With Contractures, Arterial Rupture, And Deafness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bone Fragility With Contractures, Arterial Rupture, And Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Capillary Fragility Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Capillary Fragility in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Arterial Occlusive Disease, Progressive, With Hypertension, Heart Defects, Bone Fragility, And Brachysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Increased Red Cell Osmotic Fragility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Red Cell Osmotic Fragility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Premature Delivery Because Of Cervical Insufficiency Or Membrane Fragility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Delivery Because Of Cervical Insufficiency Or Membrane Fragility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Vascular Fragility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vascular Fragility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Skin Fragility With Non-Scarring Blistering Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skin Fragility With Non-Scarring Blistering in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
decreased erythrocyte osmotic fragility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased erythrocyte osmotic fragility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased erythrocyte osmotic fragility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased erythrocyte osmotic fragility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Calvarial doughnut lesions with bone fragility Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Calvarial doughnut lesions with bone fragility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Woolly hair-skin fragility syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Woolly hair-skin fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Skin fragility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Skin fragility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Skin fragility-woolly hair-palmoplantar keratoderma syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Skin fragility-woolly hair-palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Bone fragility Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Calvarial doughnut lesions-bone fragility syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Calvarial doughnut lesions-bone fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |