| Name |
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abnormal placental size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal placental size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased placental labyrinth size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased placental labyrinth size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased placental labyrinth size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased placental labyrinth size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased placental labyrinth size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased placental labyrinth size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased placental labyrinth size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased placental labyrinth size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal placental labyrinth villi morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal placental labyrinth villi morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal placental labyrinth vasculature morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal placental labyrinth vasculature morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal placental transport Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal placental transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal placental labyrinth villi branching morphogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal placental labyrinth villi branching morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal placental transport Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placental transport phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal placental labyrinth vasculature morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placental labyrinth vasculature morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal placental thrombosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placental thrombosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal placental labyrinth villi morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placental labyrinth villi morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal placental labyrinth villi branching morphogenesis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placental labyrinth villi branching morphogenesis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
placental abruption Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease placental abruption in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
placental insufficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease placental insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
placental choriocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease placental choriocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
placental site trophoblastic tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease placental site trophoblastic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; fetal growth retardation; placental insufficiency; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
placental abruption Gene SetFrom GAD Gene-Disease Associations genes associated with the disease placental abruption in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
placental vascular complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease placental vascular complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
placental malaria Gene SetFrom GAD Gene-Disease Associations genes associated with the disease placental malaria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; placental weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; placental weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
p-glycoprotein expression, placental Gene SetFrom GAD Gene-Disease Associations genes associated with the disease p-glycoprotein expression, placental in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
placental Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term placental in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
placental growth factor-activated receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the placental growth factor-activated receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
abnormality of placental membranes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of placental membranes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Placental Insufficiency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Placental Insufficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
disorganized placental labyrinth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the disorganized placental labyrinth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
impaired placental function Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the impaired placental function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent placental labyrinth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent placental labyrinth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
placental labyrinth hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the placental labyrinth hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[placental lactogen deficiency] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [placental lactogen deficiency] phenotype from the curated OMIM Gene-Disease Associations dataset. |
{placental abruption} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {placental abruption} phenotype from the curated OMIM Gene-Disease Associations dataset. |
placental disc Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue placental disc in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
placental membrane Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue placental membrane in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
placental cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue placental cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Placental Malformation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Placental Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Placental Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Placental Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Placental Insufficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Placental Insufficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Trophoblastic Tumor, Placental Site Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Trophoblastic Tumor, Placental Site in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Placental Steroid Sulfatase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Placental Steroid Sulfatase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Placental Abnormalities (Excl Neoplasms) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Placental Abnormalities (Excl Neoplasms) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Placental Aromatase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Placental Aromatase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Placental Choriocarcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Placental Choriocarcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Exaggerated Placental Site Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Exaggerated Placental Site in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fetus Affected By Placental Transfer Of Anticonvulsant Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fetus Affected By Placental Transfer Of Anticonvulsant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Placental Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Placental Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Placental Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Placental Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Placental Membranes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Placental Membranes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
placental growth factor receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the placental growth factor receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
absent placental labyrinth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent placental labyrinth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
disorganized placental labyrinth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the disorganized placental labyrinth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
placental labyrinth hypoplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the placental labyrinth hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
impaired placental function Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired placental function phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Placental tissue cell_Placenta_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Placental tissue cell_Placenta_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
placental growth factor receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the placental growth factor receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Placental insufficiency Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Placental insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Placental abruption Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Placental abruption in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Placental choriocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Placental choriocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Placental site trophoblastic tumor Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Placental site trophoblastic tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Placental membrane Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Placental membrane in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Placental cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Placental cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Placental disc Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Placental disc in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Placental abruption Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Placental abruption phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
abnormal pancreas size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pancreas size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal size of pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal size of pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal size of the palpebral fissures Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal size of the palpebral fissures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hippocampus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal testis size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal testis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart right ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somite size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somite size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal epididymis size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal epididymis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal placenta size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal placenta size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ovary size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ovary size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal uterus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal uterus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal head size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal head size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal seminal vesicle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal seminal vesicle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prenatal growth/weight/body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prenatal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fetal growth/weight/body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal placenta labyrinth size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal placenta labyrinth size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal litter size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal litter size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cranium size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cranium size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryonic growth/weight/body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal forebrain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal forebrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal birth body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal orbit size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal orbit size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vagina size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vagina size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal postnatal growth/weight/body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal postnatal growth/weight/body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spongiotrophoblast size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spongiotrophoblast size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal midbrain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal midbrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fetal size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sternebra size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sternebra size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreas size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreas size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal oviduct size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal oviduct size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal peyer's patch size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal peyer's patch size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart left ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart left ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thymus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thymus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymph node size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal clitoris size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal clitoris size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymph organ size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph organ size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal white fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal seminiferous tubule size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal seminiferous tubule size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lung size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lung size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal white fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pituitary gland size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary gland size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal uterine cervix size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal uterine cervix size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryo size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prenatal body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prenatal body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hindbrain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hindbrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spleen size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spleen size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skeletal muscle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skeletal muscle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal skeletal muscle fiber size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal skeletal muscle fiber size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic islet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic islet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostate gland size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Abnormal Size Of Pituitary Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Size Of Pituitary Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Size Of The Palpebral Fissures Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Size Of The Palpebral Fissures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal postnatal growth/weight/body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal postnatal growth/weight/body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal somite size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal somite size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sternebra size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sternebra size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal placenta size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal placenta size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal heart left ventricle size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart left ventricle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal thymus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal thymus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryonic growth/weight/body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryonic growth/weight/body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fetal growth/weight/body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal growth/weight/body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lymph organ size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lymph organ size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal white fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal white fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal spleen size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal spleen size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal fetal size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal fetal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal testis size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal testis size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal prenatal growth/weight/body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prenatal growth/weight/body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal heart size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal heart size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal brain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal brain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal litter size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal litter size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryo size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal embryo size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal melanosome size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal melanosome size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal palatal shelf size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal palatal shelf size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cranium size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranium size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal kidney size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal kidney size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ovary size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ovary size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gallbladder size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gallbladder size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal head size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal head size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal seminiferous tubule size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal seminiferous tubule size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal liver size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pancreatic islet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pancreatic islet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal photoreceptor outer segment size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal photoreceptor outer segment size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lymph node size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lymph node size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal skeletal muscle size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal skeletal muscle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal prenatal body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal prenatal body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal neocortex size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal neocortex size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal corpus callosum size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal corpus callosum size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal midbrain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal midbrain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal embryo size Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal embryo size phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal placenta size Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal placenta size phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal head size Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal head size phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal liver size Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal liver size phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
skeletal frame size Gene SetFrom GAD Gene-Disease Associations genes associated with the disease skeletal frame size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adipocyte size, large subcutaneous abdominal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adipocyte size, large subcutaneous abdominal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bone size Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bone size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
size at birth Gene SetFrom GAD Gene-Disease Associations genes associated with the disease size at birth in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney size, newborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney size, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
reduced low-density lipoprotein particle size Gene SetFrom GAD Gene-Disease Associations genes associated with the disease reduced low-density lipoprotein particle size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic root size Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic root size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hip bone size Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hip bone size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ldl particle size and triglyceride Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ldl particle size and triglyceride in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
size Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term size in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of cellular component size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cellular component size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of multivesicular body size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of multivesicular body size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cell size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cell size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of pronephros size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of pronephros size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of endosome size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of endosome size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of blood vessel size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of blood vessel size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of peroxisome size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of peroxisome size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cell projection size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cell projection size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of vesicle size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of vesicle size biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of cell size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of cell size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of blood vessel size by renin-angiotensin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of blood vessel size by renin-angiotensin biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of tube size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of tube size biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of cell size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of cell size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of multivesicular body size involved in endosome transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of multivesicular body size involved in endosome transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of metanephros size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of metanephros size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of anatomical structure size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of anatomical structure size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of nucleus size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of nucleus size biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of kidney size Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of kidney size biological process from the curated GO Biological Process Annotations 2015 dataset. |
Hip bone size Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hip bone size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Breast size Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Breast size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Aortic root size Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Aortic root size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Spine bone size Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Spine bone size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormality of globe size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of globe size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased testicular size Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased testicular size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of muscle size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skeletal muscle fiber size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skeletal muscle fiber size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of skull size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of skull size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of mouth size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of mouth size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of corneal size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of corneal size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased size of nerve terminals Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased size of nerve terminals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased brown fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brown fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased birth body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased heart ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased heart ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased forebrain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased forebrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased tongue size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased tongue size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased heart left ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased heart left ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased small intestinal microvillus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased small intestinal microvillus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased inferior colliculus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased inferior colliculus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased atrioventricular cushion size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased atrioventricular cushion size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased atrioventricular cushion size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased atrioventricular cushion size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased spongiotrophoblast size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased spongiotrophoblast size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased axial mesoderm size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased axial mesoderm size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased long bone epiphyseal plate size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased long bone epiphyseal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased corticospinal tract size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased corticospinal tract size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased keratohyalin granule size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased keratohyalin granule size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased spleen germinal center size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased spleen germinal center size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased midbrain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased midbrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased rhombomere 4 size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased rhombomere 4 size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased anterior commissure size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased anterior commissure size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased tongue size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased tongue size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased embryo size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased embryo size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased myocardial infarction size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased myocardial infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased rhombomere 3 size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased rhombomere 3 size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased small intestinal villus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased small intestinal villus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased colliculi size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased colliculi size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased hippocampal commissure size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased hippocampal commissure size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased spongiotrophoblast size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased spongiotrophoblast size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased fetal size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased fetal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased keratohyalin granule size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased keratohyalin granule size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased mitochondria size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased mitochondria size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased lateral semicircular canal size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased lateral semicircular canal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased spleen germinal center size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased spleen germinal center size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cerebral infarction size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cerebral infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased tumor growth/size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased tumor growth/size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased litter size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased litter size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased inferior colliculus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased inferior colliculus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased heart left ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased heart left ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased midbrain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased midbrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased superior semicircular canal size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased superior semicircular canal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased dentate gyrus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased dentate gyrus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased paraxial mesoderm size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased paraxial mesoderm size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased tympanic ring size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased tympanic ring size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased myocardial infarction size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased myocardial infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased superior colliculus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased superior colliculus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased birth body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased hindbrain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased hindbrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased rhombomere 6 size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased rhombomere 6 size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased submandibular gland size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased submandibular gland size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased posterior semicircular canal size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased posterior semicircular canal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased mitochondria size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased mitochondria size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased rhombomere 5 size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased rhombomere 5 size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased white fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased hindbrain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased hindbrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased embryo size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased embryo size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased spinal cord size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased spinal cord size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased forebrain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased forebrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased corpus callosum size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased corpus callosum size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
growth/size/body phenotype Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the growth/size/body phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased hyoid bone size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased hyoid bone size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased long bone epiphyseal plate size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased long bone epiphyseal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased anterior commissure size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased anterior commissure size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased sternebra size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased sternebra size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased ventral ectodermal ridge size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased ventral ectodermal ridge size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased somite size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased somite size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased fetal size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased fetal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased white fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased heart right ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased heart right ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased spinal cord size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased spinal cord size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased skeletal muscle fiber size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased skeletal muscle fiber size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased variability of skeletal muscle fiber size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased variability of skeletal muscle fiber size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased placenta intervillous maternal lacunae size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased placenta intervillous maternal lacunae size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased palatine bone horizontal plate size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased palatine bone horizontal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased submandibular gland size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased submandibular gland size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased body size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased brown fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brown fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brain internal capsule size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brain internal capsule size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased maxillary shelf size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased maxillary shelf size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased lactotroph cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased lactotroph cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased skeletal muscle fiber size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased skeletal muscle fiber size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased superior colliculus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased superior colliculus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased litter size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased litter size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased rhombomere 3 size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased rhombomere 3 size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased skeletal muscle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased skeletal muscle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased brain size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased anterior vermis size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased anterior vermis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased rhombomere 1 size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased rhombomere 1 size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brown fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brown fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased axial mesoderm size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased axial mesoderm size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased tumor growth/size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased tumor growth/size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased ventral retina size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased ventral retina size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased corticotroph cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased corticotroph cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased tegmentum size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased tegmentum size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cerebral infarction size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cerebral infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased skeletal muscle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased skeletal muscle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brown fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brown fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased somatotroph cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased somatotroph cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased hyoid bone size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased hyoid bone size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased rhombomere 1 size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased rhombomere 1 size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased white fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased parotid gland size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased parotid gland size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased white fat cell size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
[bone size quantitative trait locus 3] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [bone size quantitative trait locus 3] phenotype from the curated OMIM Gene-Disease Associations dataset. |
{bone size qtl} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {bone size qtl} phenotype from the curated OMIM Gene-Disease Associations dataset. |
Decreased Size Of Nerve Terminals Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Decreased Size Of Nerve Terminals in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Breast Size Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Breast Size in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Skeletal Muscle Fiber Size Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Skeletal Muscle Fiber Size in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Size Of Penis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Size Of Penis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Mouth Size Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Mouth Size in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Globe Size Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Globe Size in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Size Of The Mandible Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Size Of The Mandible in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Muscle Size Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Muscle Size in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Skull Size Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Skull Size in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
regulation of cell size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cell size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of peroxisome size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of peroxisome size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of endosome size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of endosome size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lysosome size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lysosome size biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of cell size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of cell size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of vesicle size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of vesicle size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of pronephros size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of pronephros size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of thalamus size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of thalamus size biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of cell size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of cell size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cellular component size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cellular component size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of multivesicular body size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of multivesicular body size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of metanephros size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of metanephros size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of kidney size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of kidney size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of nucleus size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of nucleus size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of autophagosome size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of autophagosome size biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cell projection size Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cell projection size biological process from the curated GO Biological Process Annotations 2023 dataset. |
decreased embryo size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased embryo size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased spongiotrophoblast size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased spongiotrophoblast size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased tympanic ring size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased tympanic ring size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased birth body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased birth body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased rhombomere 1 size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased rhombomere 1 size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased lateral semicircular canal size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased lateral semicircular canal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased fetal size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fetal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased somite size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased somite size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased spinal cord size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased spinal cord size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased midbrain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased midbrain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased long bone epiphyseal plate size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased long bone epiphyseal plate size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased litter size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased litter size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased skeletal muscle fiber size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased skeletal muscle fiber size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased forebrain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased forebrain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased atrioventricular cushion size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased atrioventricular cushion size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased inferior colliculus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased inferior colliculus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased superior colliculus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased superior colliculus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased corpus callosum size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased corpus callosum size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased striatum size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased striatum size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased anterior vermis size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased anterior vermis size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased inferior colliculus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased inferior colliculus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased atrioventricular cushion size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased atrioventricular cushion size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased myocardial infarct size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased myocardial infarct size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased tumor growth/size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased tumor growth/size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased hippocampal commissure size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased hippocampal commissure size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased anterior commissure size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased anterior commissure size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased litter size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased litter size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased hindbrain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased hindbrain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased posterior semicircular canal size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased posterior semicircular canal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased superior semicircular canal size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased superior semicircular canal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased mitochondrial size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased mitochondrial size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased ventromedial hypothalamic nucleus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased ventromedial hypothalamic nucleus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased paraxial mesoderm size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased paraxial mesoderm size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased axial mesoderm size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased axial mesoderm size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased somatotroph cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased somatotroph cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brain internal capsule size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain internal capsule size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased long bone epiphyseal plate size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased long bone epiphyseal plate size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased rhombomere 3 size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased rhombomere 3 size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased rhombomere 5 size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased rhombomere 5 size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased rhombomere 6 size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased rhombomere 6 size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased spinal cord size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased spinal cord size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased spleen germinal center size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased spleen germinal center size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased myocardial infarct size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased myocardial infarct size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cerebral infarct size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cerebral infarct size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brown fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brown fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased variability of skeletal muscle fiber size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased variability of skeletal muscle fiber size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased spongiotrophoblast size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased spongiotrophoblast size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased tongue size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased tongue size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased palatal shelf size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased palatal shelf size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased autopod size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased autopod size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased striatum size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased striatum size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cerebral infarct size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cerebral infarct size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased tongue size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased tongue size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased fetal size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased fetal size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased birth body size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased birth body size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased nipple size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased nipple size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased white fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased keratohyalin granule size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased keratohyalin granule size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased tumor growth/size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased tumor growth/size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased hippocampal fornix size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased hippocampal fornix size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased white fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased lactotroph cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased lactotroph cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased autopod size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased autopod size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased palatine bone horizontal plate size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased palatine bone horizontal plate size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased maxillary shelf size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased maxillary shelf size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased skeletal muscle fiber size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased skeletal muscle fiber size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased spleen germinal center size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased spleen germinal center size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased superior colliculus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased superior colliculus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brown fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brown fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased midbrain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased midbrain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased substantia nigra size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased substantia nigra size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased small intestinal villus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased small intestinal villus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased ventral retina size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased ventral retina size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brown fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brown fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased rhombomere 1 size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased rhombomere 1 size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased heart left ventricle size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased heart left ventricle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased white fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased rhombomere 3 size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased rhombomere 3 size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased keratohyalin granule size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased keratohyalin granule size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased heart ventricle size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased heart ventricle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased heart right ventricle size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased heart right ventricle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased parotid gland size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased parotid gland size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased hippocampal fornix size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased hippocampal fornix size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased optic chiasm size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased optic chiasm size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased submandibular gland size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased submandibular gland size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased round window size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased round window size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased corticospinal tract size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased corticospinal tract size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased axial mesoderm size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased axial mesoderm size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased femur size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased femur size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased radius size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased radius size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased sternebra size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased sternebra size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased embryo size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased embryo size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased ventral ectodermal ridge size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased ventral ectodermal ridge size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased palatal shelf size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased palatal shelf size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased hindbrain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased hindbrain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased anterior commissure size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased anterior commissure size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased heart right ventricle size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased heart right ventricle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased rhombomere 4 size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased rhombomere 4 size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased forebrain size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased forebrain size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased hyoid bone size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased hyoid bone size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cornea size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cornea size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased mouth size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased mouth size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased optic chiasm size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased optic chiasm size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased heart left ventricle size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased heart left ventricle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased skeletal muscle size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased skeletal muscle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased colliculi size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased colliculi size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased small intestinal microvillus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased small intestinal microvillus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cochlear VIII nucleus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cochlear VIII nucleus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased rhombomere 4 size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased rhombomere 4 size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brown fat cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brown fat cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased subiculum size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased subiculum size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased white fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased hyoid bone size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased hyoid bone size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased pons size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased pons size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased somatotroph cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased somatotroph cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cornea size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cornea size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased neocortex size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased neocortex size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased skeletal muscle size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased skeletal muscle size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased tegmentum size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased tegmentum size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased placenta intervillous maternal lacunae size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased placenta intervillous maternal lacunae size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased radius size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased radius size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased mitochondrial size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased mitochondrial size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased corticotroph cell size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased corticotroph cell size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased submandibular gland size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased submandibular gland size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased hindlimb autopod size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased hindlimb autopod size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased dentate gyrus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased dentate gyrus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced sympathetic cervical ganglion size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced sympathetic cervical ganglion size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased corpus callosum size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased corpus callosum size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brain external capsule size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brain external capsule size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased amygdala size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased amygdala size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased neocortex size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased neocortex size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased parotid gland size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased parotid gland size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased astrocyte size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased astrocyte size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased stria medullaris size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased stria medullaris size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pontine nuclei size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pontine nuclei size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased dentate gyrus size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased dentate gyrus size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
growth/size/body region phenotype Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the growth/size/body region phenotype phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cingulate cortex size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cingulate cortex size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cingulate cortex size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cingulate cortex size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased primary motor cortex size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased primary motor cortex size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased hippocampal fimbria size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased hippocampal fimbria size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased mouth size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased mouth size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased primary motor cortex size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased primary motor cortex size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased retrosplenial granular cortex size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased retrosplenial granular cortex size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased hippocampal fimbria size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased hippocampal fimbria size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased pons size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased pons size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased mammillothalamic tract size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased mammillothalamic tract size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased habenula size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased habenula size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased oval window size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased oval window size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased heart left ventricle size Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased heart left ventricle size phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
decreased heart left ventricle size Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased heart left ventricle size phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
decreased brain size Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the decreased brain size phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
increased brain size Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the increased brain size phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
regulation of cell size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cell size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of peroxisome size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of peroxisome size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of endosome size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of endosome size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lysosome size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lysosome size biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of cell size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of cell size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of vesicle size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of vesicle size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of pronephros size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of pronephros size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of thalamus size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of thalamus size biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of cell size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of cell size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of metanephros size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of metanephros size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of kidney size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of kidney size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of nucleus size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of nucleus size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of autophagosome size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of autophagosome size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cellular component size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cellular component size biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cell projection size Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cell projection size biological process from the curated GO Biological Process Annotations 2025 dataset. |
Antitragus size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Antitragus size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lobe size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lobe size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Breast size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Breast size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Nose size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nose size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Aortic root size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aortic root size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Optic disc size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Optic disc size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Spine bone size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spine bone size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Adult body size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Adult body size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Uterine fibroid size (maximum dimension) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Uterine fibroid size (maximum dimension) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Uterine fibroid size (maximum volume) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Uterine fibroid size (maximum volume) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Body size at age 10 Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body size at age 10 phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hip bone size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip bone size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Itch intensity from mosquito bite adjusted by bite size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Itch intensity from mosquito bite adjusted by bite size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Intertrochanteric region size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Intertrochanteric region size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Trochanter size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Trochanter size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Mosquito bite size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mosquito bite size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Non-muscle-invasive bladder cancer tumour size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Non-muscle-invasive bladder cancer tumour size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Thyroid hormone metabolism, abnormal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Reflex, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Reflex, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Neutrophil Chemotactic Response, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutrophil Chemotactic Response, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Thyroid Hormone Metabolism, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset. |
abnormal retinal correspondence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormal splicing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal splicing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal; brugada syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal; brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal urogenital development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal urogenital development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal fibrin polymerization and thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal fibrin polymerization and thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormal cannabidiol Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the abnormal cannabidiol ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
abnormal eye physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal intraocular pressure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eating behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eating behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal thrombosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal thrombosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal leukocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal leukocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal iris pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal iris pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bone structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bone structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal serum iron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal serum iron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal emotion/affect behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bleeding Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bleeding phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair quantity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair quantity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal ekg Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal ekg phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal axial skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal immunoglobulin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal immunoglobulin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal monocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal monocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neutrophil cell number Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neutrophil cell number phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal facial shape Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal facial shape phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
acquired abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glomerular filtration rate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal testosterone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal testosterone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal joint morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal joint morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal motor neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal biliary tract morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal biliary tract morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal genital system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal genital system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal appendicular skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal cortical bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal respiratory system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal respiratory system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal number of teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal circulating creatinine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal circulating creatinine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal autonomic nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal muscle tone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal muscle tone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal diaphysis morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal diaphysis morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal spermatogenesis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal spermatogenesis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hemoglobin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hemoglobin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glucose homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of hand bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone structure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone structure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal branching pattern of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal maternal serum screening Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal maternal serum screening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rod and cone electroretinograms Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rod and cone electroretinograms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal albumin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal albumin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enchondral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enchondral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet membrane protein expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet membrane protein expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondria in muscle tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondria in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal central microtubular pair morphology of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet granules Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet granules phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal subcutaneous fat tissue distribution Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal subcutaneous fat tissue distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lung lobation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lung lobation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal flash visual evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine phosphate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine phosphate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal drinking behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal drinking behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal fear/anxiety-related behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal fear/anxiety-related behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal corticomedullary differentiation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal humeral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal humeral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delayed hypersensitivity skin test Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein n-linked glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein n-linked glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal echocardiogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal echocardiogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum ferritin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axial skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal calcification of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal calcification of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal testosterone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal testosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal speech discrimination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal speech discrimination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal genital system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal genital system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal liver function tests during pregnancy Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal liver function tests during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal trabecular bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal trabecular bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metacarpal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metacarpal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal t3/t4 ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal t3/t4 ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal posturing Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal posturing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal natural killer cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal natural killer cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal immunoglobulin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal immunoglobulin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal monocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal monocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrial arrangement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrial arrangement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating renin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating renin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal retinal folds Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal retinal folds phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine sodium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine sodium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vestibulo-ocular reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vestibulo-ocular reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral pedicle morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral pedicle morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal tendon morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal tendon morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glucose homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal leukocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal leukocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal tarsal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal spermatogenesis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal spermatogenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine potassium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine potassium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal synaptic transmission at the neuromuscular junction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal synaptic transmission at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary light reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary light reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pyramidal signs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pyramidal signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pigmentation of the oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pigmentation of the oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of incisors Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal localization of kidney Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal localization of kidney phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal elasticity of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal elasticity of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet volume Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vas deferens morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vas deferens morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal muscle tone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal muscle tone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lower motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lower motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ciliary motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ciliary motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrioventricular conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metatarsal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metatarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal st segment Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal st segment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sweat homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sweat homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nasal base Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nasal base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pelvis bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pelvis bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of the pubic bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal isoelectric focusing of serum transferrin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal isoelectric focusing of serum transferrin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hemoglobin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hemoglobin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nasal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nasal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal concentration of calcium in blood Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal concentration of calcium in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal emotion/affect behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal epiphyseal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine cytology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine cytology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal palmar dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal palmar dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal csf lactate level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal csf lactate level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facial shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal joint morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal joint morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral segmentation and fusion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral segmentation and fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal oral glucose tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal oral glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone collagen fibril morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone collagen fibril morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delivery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delivery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal middle ear reflexes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal middle ear reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondrial morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondrial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cervical curvature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cervical curvature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bleeding Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondrial shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondrial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal auditory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal activity of mitochondrial respiratory chain Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal location of ears Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal location of ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cns myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cns myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eating behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eating behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrioventricular connection Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrioventricular connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ventriculo-arterial connection Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ventriculo-arterial connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal anterior horn cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal anterior horn cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper to lower segment ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal form of the vertebral bodies Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine output Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine output phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal blistering of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal blistering of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal diaphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal diaphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cholesterol homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cholesterol homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine citrate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine citrate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hand morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hand morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair quantity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair quantity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal anatomic location of the heart Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal anatomic location of the heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iron deposition in mitochondria Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iron deposition in mitochondria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating aldosterone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating aldosterone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating creatinine level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating creatinine level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal large intestine physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal large intestine physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facial expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine chloride concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine chloride concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vascular physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vascular physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal heart morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal heart morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair laboratory examination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair laboratory examination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal retinal pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal retinal pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the palpebral fissure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lymphocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lymphocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal conjugate eye movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal conjugate eye movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pulmonary lymphatics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pulmonary lymphatics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pattern of respiration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pattern of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair whorl Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair whorl phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal connection of the cardiac segments Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal connection of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cartilage collagen Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cartilage collagen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal umbilical stump bleeding Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal umbilical stump bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal social behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal social behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical gyration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical gyration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum iron Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum iron phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of permanent teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sex determination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sex determination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal prolactin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal prolactin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory epithelium morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory epithelium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axonemal organization of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axonemal organization of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal foot bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal foot bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal neutrophil cell number Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal neutrophil cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cone-mediated electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cone-mediated electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal basal ganglia mri signal intensity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal basal ganglia mri signal intensity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sensory nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal muscle glycogen content Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal muscle glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal appendicular skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hand bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of erythroid precursors Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of erythroid precursors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine magnesium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine magnesium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rapid eye movement (rem) sleep Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glucose tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ekg Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ekg phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal levels of creatine kinase in blood Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal levels of creatine kinase in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ejaculation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ejaculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urinary electrolyte concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urinary electrolyte concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal finger flexion creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metaphyseal trabeculation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metaphyseal trabeculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal umbilical cord blood vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal umbilical cord blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal head movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal head movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
acquired abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facility in opposing the shoulders Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facility in opposing the shoulders phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal migration of corneal endothelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal migration of corneal endothelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal intraocular pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal intraocular pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the frontal region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the frontal region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urinary sulfate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urinary sulfate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal spatial orientation of the cardiac segments Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal spatial orientation of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rib ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glomerular filtration rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sternal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sternal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the occiput Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the occiput phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal involuntary eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metaphyseal vascular invasion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metaphyseal vascular invasion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enzyme/coenzyme activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enzyme/coenzyme activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cartilage morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cartilage morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral action potential amplitude Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral action potential amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Reflex, Abnormal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Reflex, Abnormal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Spindle assembly abnormal protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spindle assembly abnormal protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DMRT/protein doublesex/protein male abnormal 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein male abnormal 21-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein male abnormal 21-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Abnormal spindle-like microcephaly-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Abnormal spindle-like microcephaly-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal clitoris morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal clitoris morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lung volume Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lung volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basilar membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basilar membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural fold elevation formation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensory capabilities/reflexes/nociception Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensory capabilities/reflexes/nociception phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to anesthetic Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to anesthetic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal trigeminal ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal trigeminal ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory brainstem response waveform shape Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response waveform shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal photoreceptor layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal photoreceptor layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bradykinin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bradykinin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fetal derived definitive erythrocyte cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paravertebral ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paravertebral ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasal cavity morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasal cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary sex determination Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary sex determination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus stratum lacunosum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus stratum lacunosum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gallbladder morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gallbladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ectomesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ectomesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male urethra morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone marrow cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zona glomerulosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zona glomerulosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal surfactant secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal surfactant secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum fastigial nucleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum fastigial nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal social/conspecific interaction Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal social/conspecific interaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tooth morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neutrophil differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neutrophil differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vomer bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vomer bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endplate potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endplate potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sagittal suture morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sagittal suture morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal semicircular canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal semicircular canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal estrous cycle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal estrous cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive t cell differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive t cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuron differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuron differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone metaphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vascular endothelial cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular endothelial cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sympathetic neuron innervation pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sympathetic neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal melanosome transport Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal melanosome transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inferior colliculus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inferior colliculus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tongue muscle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tongue muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal inner nuclear layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal keratinocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to methamphetamine Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to methamphetamine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory brainstem response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal macrophage derived foam cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal macrophage derived foam cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart left atrium weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart left atrium weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal malleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal malleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala vestibuli morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala vestibuli morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pupillary reflex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pupillary reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal interdigital cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal schwann cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal schwann cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior definitive endoderm morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior definitive endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal keratinocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal protein reabsorption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal protein reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal habenula morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal habenula morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine antidiuretic hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine antidiuretic hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryonic tissue morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal laryngeal mucosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal laryngeal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasma membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasma membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating angiotensinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating angiotensinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal corneocyte envelope morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corneocyte envelope morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primordial ovarian follicle number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostate gland dorsolateral lobe morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland dorsolateral lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular nerve morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal melanocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parametrial fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parametrial fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal effector t cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal effector t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine aldosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal roof plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal roof plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone healing Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone healing phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rhombomere 4 morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rhombomere 4 morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal snout morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal snout morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal optic disc morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic disc morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parasympathetic ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parasympathetic ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blinking Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blinking phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellar molecular layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-1 alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-1 alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thyroid gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroid gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal efferent ductules of testis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal efferent ductules of testis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal periocular mesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal periocular mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purkinje cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pancreatic peptide level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pancreatic peptide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal frontonasal prominence morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal frontonasal prominence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gas homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gas homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestinal mucosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestinal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dermis papillary layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dermis papillary layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair shaft morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair shaft morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cellular replicative senescence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cellular replicative senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal throat morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal throat morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasolacrimal duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasolacrimal duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal first pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal first pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal loop of henle descending limb morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal loop of henle descending limb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal triiodothyronine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal visual acuity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating sulfate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating sulfate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parturition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parturition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala tympani morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala tympani morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external urethral orifice morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external urethral orifice morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal chorioallantoic fusion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal chorioallantoic fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purkinje cell dendrite morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell dendrite morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lens development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lens development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pituitary diverticulum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary diverticulum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal arteriole morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal arteriole morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal outer hair cell stereociliary bundle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal outer hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic endocrine progenitor cell proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic endocrine progenitor cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rosenthal canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rosenthal canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pr interval Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal enterocyte apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enterocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal glomerulus basement membrane thickness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal superior vagus ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal superior vagus ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal melanoblast morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal melanoblast morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal single cell response threshold Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal single cell response threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dermis reticular layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dermis reticular layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal body height Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body height phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelial cell primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal optic stalk morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic stalk morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural tube mantle layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural tube mantle layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior cardinal vein morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior cardinal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal tubule epithelial cell primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal tubule epithelial cell primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intramembranous bone ossification Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear distance/ position Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal maxillary sinus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal maxillary sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal otic vesicle development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal otic vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymph node b cell domain morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node b cell domain morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lactate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lactate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasmacytoid dendritic cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasmacytoid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal rod cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal digestive system development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal digestive system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory summating potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory summating potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paired-pulse inhibition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paired-pulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic arch and aortic arch branch attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch and aortic arch branch attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal ganglion cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal ganglion cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal postnatal growth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal postnatal growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal memory t cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal miniature inhibitory postsynaptic currents Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal miniature inhibitory postsynaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal axillary lymph node morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal axillary lymph node morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal costal cartilage morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal costal cartilage morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal splenocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal splenocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating chemokine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating chemokine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum posterior vermis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum posterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thalamus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thalamus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair medulla air spaces Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair medulla air spaces phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zigzag hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zigzag hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal xenobiotic induced morbidity/mortality Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pons morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pons morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell anergy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rr interval Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic acinar cell zymogen granule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic acinar cell zymogen granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal meibomian gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal meibomian gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum vermis lobule ii morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule ii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tubuloglomerular feedback response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tubuloglomerular feedback response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b wave amplitude Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b wave amplitude phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine organic cation level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine organic cation level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryo attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal myogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal myogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory bulb granule cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory bulb granule cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |