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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 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 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 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. |
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. |
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. |
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. |
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. |
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 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 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. |
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. |
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. |
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. |
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. |
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 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 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. |
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. |
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. |
abnormality of muscle morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pectoral muscle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pectoral muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of muscle morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of muscle fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of Masticatory Muscle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Masticatory Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Masseter Muscle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Masseter Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Muscle Fibers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Muscle Fibers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Abnormality Related To Mitochondrial Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Abnormality Related To Mitochondrial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Tongue Muscle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Tongue Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Inferior Oblique Extraocular Muscle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Inferior Oblique Extraocular Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
response to muscle activity involved in regulation of muscle adaptation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to muscle activity involved in regulation of muscle adaptation biological process from the curated GO Biological Process Annotations 2015 dataset. |
cardiac muscle cell-cardiac muscle cell adhesion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cardiac muscle cell-cardiac muscle cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset. |
skeletal muscle satellite cell maintenance involved in skeletal muscle regeneration Gene SetFrom GO Biological Process Annotations 2015 genes participating in the skeletal muscle satellite cell maintenance involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to muscle inactivity involved in regulation of muscle adaptation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to muscle inactivity involved in regulation of muscle adaptation biological process from the curated GO Biological Process Annotations 2015 dataset. |
Muscle-fast muscle cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Muscle-fast muscle cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Muscle-skeletal muscle satellite stem cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Muscle-skeletal muscle satellite stem cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Muscle-slow muscle cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Muscle-slow muscle cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
Muscle-smooth muscle cell Gene SetFrom Tabula Sapiens Gene-Cell Associations genes with high or low expression in Muscle-smooth muscle cell relative to other cell types from the Tabula Sapiens Gene-Cell Associations dataset. |
cardiac muscle cell-cardiac muscle cell adhesion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cardiac muscle cell-cardiac muscle cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset. |
Human - Fetal Development - L2 - Muscle-Skeletal muscle cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Skeletal muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Fetal Development - L2 - Muscle-Smooth muscle cells Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Fetal Development - L2 - Muscle-Smooth muscle cells cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
cardiac muscle cell-cardiac muscle cell adhesion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cardiac muscle cell-cardiac muscle cell adhesion biological process from the curated GO Biological Process Annotations 2025 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Hypertelorism with esophageal abnormality and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormality of glucagon secretion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormality of glucagon secretion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrin secretion abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrin secretion abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadasil; chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
torsion abnormality; vascular malformations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease torsion abnormality; vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; lymphocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
smooth pursuit eye movement abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormality Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormality in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormality of vitamin metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endometrium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endometrium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forearm bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forearm bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the integument Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the integument phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin d metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of myeloid leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral subcortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral subcortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of divalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stomach Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stomach phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycolipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of connective tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of connective tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aortic valve Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cellular immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cellular immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hearing abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hearing abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune serum protein physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of oral mucosa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of oral mucosa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urethra Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urethra phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of brain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of brain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endocrine system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endocrine system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cerebral artery Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cerebral artery phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the breast Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the breast phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the autonomic nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the autonomic nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
eeg abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the eeg abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femur Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femur phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin a metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the calf Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the calf phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of potassium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the carotid arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the carotid arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of retinal arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the kidney Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the kidney phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circle of willis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circle of willis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hand Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hand phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pituitary gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pituitary gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the myocardium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the myocardium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the biliary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the biliary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cell cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cell cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of von willebrand factor Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of long bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thrombocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thrombocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of neutrophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of neutrophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hip bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the iris Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the iris phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of hair pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
mesangial abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the mesangial abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin b metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating fibrinogen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating fibrinogen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the adrenal glands Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the adrenal glands phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the respiratory system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of phalanx of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the musculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the musculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral white matter Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the duodenum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the duodenum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull base Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the astrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the astrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of basophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of basophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the face Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the face phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the male genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the male genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of facial skeleton Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of facial skeleton phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gingiva Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gingiva phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the large intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lung Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lung phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating hormone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating hormone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the placenta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the placenta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ankles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ankles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the heart valves Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the heart valves phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of aromatic amino acid family metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eye movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ovary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ovary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the prostate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the prostate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of digit Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of digit phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limbs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the testis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the testis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental eruption Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental eruption phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the clavicle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the clavicle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of homocysteine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the knees Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the knees phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coronary arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coronary arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cardiovascular system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cardiovascular system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin adnexa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pleura Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pleura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of interleukin secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of interleukin secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood and blood-forming tissues Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of transition element cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of tryptophan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of tryptophan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of head or neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of head or neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mandible Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mandible phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional respiratory abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone mineral density Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of humoral immunity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of humoral immunity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
neurodevelopmental abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neurodevelopmental abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of taste sensation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of taste sensation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of renin-angiotensin system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of renin-angiotensin system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pancreas physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skeletal system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of primary teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thorax Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thorax phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thyroid gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thyroid gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdomen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdomen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrospinal fluid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrospinal fluid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the menstrual cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the menstrual cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
behavioral abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the behavioral abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the oral cavity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the oral cavity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cholesterol metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cholesterol metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of granulocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of granulocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of monovalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the fundus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the fundus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forebrain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forebrain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the tongue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the tongue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of acid-base homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebrae Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebrae phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the spinal cord Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
vascular skin abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of iron homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of iron homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of refraction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of refraction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood volume homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dna repair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dna repair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nose Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nose phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nitrogen compound homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nitrogen compound homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of erythrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of erythrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of liposaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of liposaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glomerulus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of unsaturated fatty acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating protein level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating protein level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of copper homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
prenatal maternal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humeral diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humeral diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
phenotypic abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the phenotypic abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uterus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uterus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of female internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the metaphyses Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the metaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the common coagulation pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fatty-acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genitourinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genitourinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cytokine secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cytokine secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
growth abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the growth abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the choroid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the choroid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the globe Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the globe phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of radial diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of radial diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sodium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sodium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear ossicles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the monocyte/macrophage lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb joint Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uvea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uvea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary tract abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary tract abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdominal organs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdominal organs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the esophagus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the esophagus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retina Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retina phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the penis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the penis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood circulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the radius Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the radius phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of urine homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of urine homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the costochondral junction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the costochondral junction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral cortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
venous abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the venous abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of extrapyramidal motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone marrow cell morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the liver Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the liver phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of proteoglycan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of proteoglycan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fluid regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fluid regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pylorus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pylorus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of adipose tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of adipose tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior pituitary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nasopharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nasopharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intervertebral disk Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intervertebral disk phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stapes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stapes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gallbladder Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gallbladder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coagulation cascade Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coagulation cascade phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of zinc homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of zinc homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pelvic girdle bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
generalized abnormality of skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricular outflow tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carbohydrate metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glial cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glial cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper arm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ulna Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ulna phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal endothelium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal endothelium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lymphocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lymphocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal thickness Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mouth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mouth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vitamin b12 metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of magnesium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of magnesium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the small intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genital system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genital system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aorta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aorta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the female genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the female genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humerus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humerus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiovascular system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of complement system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of complement system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the erythroid lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
chorioretinal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the chorioretinal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sulfur amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sulfur amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating cortisol level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating cortisol level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prothrombin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prothrombin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of coagulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of coagulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cervical spine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cervical spine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carboxylic acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pancreas Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pancreas phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skeletal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skeletal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lens Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lens phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body weight Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of temperature regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of temperature regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the systemic arterial tree Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the systemic arterial tree phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the rib cage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the rib cage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycoprotein metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin e metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retinal vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of ion homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of ion homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of macrophages Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of macrophages phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of calcium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of calcium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body height Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body height phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of polysaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of polysaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intrinsic pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intrinsic pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eosinophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eosinophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the macula Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the macula phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of epidermal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of epidermal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of higher mental function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of higher mental function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ribs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ribs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nucleobase metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nucleobase metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the forearm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the forearm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of purine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of purine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of serum cytokine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of serum cytokine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating leptin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating leptin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nephron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nephron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating glucocorticoid level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating glucocorticoid level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the level of lipoprotein cholesterol Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the level of lipoprotein cholesterol phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the falx cerebri Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the falx cerebri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of myeloid leukocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of gastrointestinal vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of gastrointestinal vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the extraocular muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choanae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choanae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycolipid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal cavity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal cavity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the immune system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the immune system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of reticulocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of reticulocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cochlea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of von willebrand factor Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cerebellar peduncle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the gingiva Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the gingiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lung Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lung phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the basal ganglia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vena cava Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vena cava phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of sharpey fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of sharpey fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cornea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metacarpophalangeal joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metacarpophalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intrahepatic bile duct Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intrahepatic bile duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of fluid regulation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of fluid regulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the philtrum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dentate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fallopian tube Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of secondary sexual hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pineal gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pineal gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the crus of the helix Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the crus of the helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acetabulum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acetabulum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sense of smell Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sense of smell phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of permanent molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of permanent molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the parathyroid physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the parathyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the achilles tendon Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the achilles tendon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the myocardium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the myocardium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of complement system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of complement system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the medullary cavity of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycoprotein metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of blood glucose concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of blood glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal tubule Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal tubule phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the shoulder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the shoulder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 3rd toe Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of chromosome condensation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prostaglandin metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prostaglandin metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neurodevelopmental abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the neurodevelopmental abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of connective tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of connective tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thumb phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the odontoid process Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alanine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alanine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atlantoaxial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the atlantoaxial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lower limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lower limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thrombocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thrombocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the posterior pituitary Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior chamber Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vestibulocochlear nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vestibulocochlear nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prenatal development or birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of binocular vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of binocular vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal septum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cation homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thyroid gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thyroid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forebrain morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forebrain morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cerebral artery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cerebral artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choroid plexus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choroid plexus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating protein level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating protein level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pancreas morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the seventh cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the seventh cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the labia minora Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the palmar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary tract abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary tract abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the lymphoid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the lymphoid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized abnormality of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the glial cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the glial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aryepiglottic fold Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aryepiglottic fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the erythroid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prothrombin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prothrombin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the subungual region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the subungual region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thyroid morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thyroid morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the scalp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the retinal pigment epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal collecting system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal collecting system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the middle phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nerves Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acoustic reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acoustic reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of potassium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tubulointerstitial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the tubulointerstitial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dental pulp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dental pulp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cysteine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cysteine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thenar eminence Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of ganglioside metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of ganglioside metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of humoral immunity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of humoral immunity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sixth cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sixth cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of calvarial morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of calvarial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hip joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hip joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the humeral metaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the humeral metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of urine bicarbonate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of urine bicarbonate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the genitourinary system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the genitourinary system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lymphatic vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fascia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fascia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ear Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the liver Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the liver phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of dental color Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of dental color phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alkaline phosphatase activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alkaline phosphatase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the larynx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the larynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chorioretinal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the chorioretinal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating hormone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating hormone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the salivary glands Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the salivary glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of primary molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of primary molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of copper homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of copper homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sacroiliac joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sacroiliac joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the diaphragm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |