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abnormality of the posterior hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
low posterior hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the low posterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Low Posterior Hairline Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Posterior Hairline in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype 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 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 Hairline Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Hairline in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Frontal Hairline Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Frontal Hairline in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality of the hairline Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of the hairline phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
low anterior hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the low anterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
high anterior hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the high anterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Low Anterior Hairline Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Anterior Hairline in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
High Anterior Hairline Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Anterior Hairline in GWAS and other genetic association datasets from the DisGeNET Gene-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 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 posterior cranial fossa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior cranial fossa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of The Posterior Cranial Fossa Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Posterior Cranial Fossa in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
paracentral lobule, posterior part, left, bank of cingulate sulcus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in paracentral lobule, posterior part, left, bank of cingulate sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
posterior orbital gyrus, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior orbital gyrus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
postcentral gyrus, left, bank of the posterior central sulcus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in postcentral gyrus, left, bank of the posterior central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
paracentral lobule, posterior part, right, bank of cingulate sulcus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in paracentral lobule, posterior part, right, bank of cingulate sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
posterior group of nuclei, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
paracentral lobule, posterior part, left, lateral bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in paracentral lobule, posterior part, left, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
posterior hypothalamic area, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior hypothalamic area, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
posterior hypothalamic area, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior hypothalamic area, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
posterior group of nuclei, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
paracentral lobule, posterior part, right, lateral bank of gyrus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in paracentral lobule, posterior part, right, lateral bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
postcentral gyrus, right, bank of the posterior central sulcus Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in postcentral gyrus, right, bank of the posterior central sulcus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
posterior orbital gyrus, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior orbital gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
Posterior amygdalar nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior amygdalar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Ventral posterior complex of the thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Ventral posterior complex of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Bed nuclei of the stria terminalis, posterior division, interfascicular nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, posterior division, interfascicular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
basolateral amygdaloid nucleus, posterior part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in basolateral amygdaloid nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posterior (ventral) nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posterior (ventral) nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
interstitial nucleus of the posterior limb of the anterior commissure Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in interstitial nucleus of the posterior limb of the anterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior pretectal nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior pretectal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, medial zone, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, medial zone, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, medial zone, layer 2 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, medial zone, layer 2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, medial zone, layer 3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, medial zone, layer 3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior parietal association areas, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior parietal association areas, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior parietal association areas, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior parietal association areas, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Basomedial amygdalar nucleus, posterior part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basomedial amygdalar nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior hypothalamic nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
magnocellular interstitial nucleus of the posterior commissure Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in magnocellular interstitial nucleus of the posterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posterior triangular nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posterior triangular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Periventricular hypothalamic nucleus, posterior part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Periventricular hypothalamic nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posterior part of Int Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posterior part of Int relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, lateral zone Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, lateral zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
basomedial amygdaloid nucleus, posterior part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in basomedial amygdaloid nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Paraventricular hypothalamic nucleus, magnocellular division, posterior magnocellular part, lateral zone Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, magnocellular division, posterior magnocellular part, lateral zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Nucleus of the posterior commissure Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the posterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Basolateral amygdalar nucleus, posterior part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Basolateral amygdalar nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
lateral posterior nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lateral posterior nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior complex of the thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior complex of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior limiting nucleus of the thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior limiting nucleus of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Bed nuclei of the stria terminalis, posterior division, transverse nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, posterior division, transverse nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Dorsomedial nucleus of the hypothalamus, posterior part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Dorsomedial nucleus of the hypothalamus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Bed nuclei of the stria terminalis, posterior division, strial extension Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, posterior division, strial extension relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Lateral posterior nucleus of the thalamus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral posterior nucleus of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, lateral zone, layer 2 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, lateral zone, layer 2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, lateral zone, layer 3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, lateral zone, layer 3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, lateral zone, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, lateral zone, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Paraventricular hypothalamic nucleus, magnocellular division, posterior magnocellular part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Paraventricular hypothalamic nucleus, magnocellular division, posterior magnocellular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posterior paraventricular nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posterior paraventricular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part, medial zone Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part, medial zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior parietal association areas, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior parietal association areas, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior parietal association areas, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior parietal association areas, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Bed nuclei of the stria terminalis, posterior division Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, posterior division relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Cortical amygdalar area, posterior part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cortical amygdalar area, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Anterior hypothalamic nucleus, posterior part Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Anterior hypothalamic nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
parvicellular interstitial nucleus of the posterior commissure Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in parvicellular interstitial nucleus of the posterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posterior intralaminar nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posterior intralaminar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Bed nuclei of the stria terminalis, posterior division, principal nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Bed nuclei of the stria terminalis, posterior division, principal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior parietal association areas Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior parietal association areas relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posterior tegmental nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posterior tegmental nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior parietal association areas, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior parietal association areas, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Posterior parietal association areas, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Posterior parietal association areas, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posterior part of anterior hypothalamic nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in posterior part of anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
ventral posterior parvicellular nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in ventral posterior parvicellular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_25 pcw_F_12948 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_25 pcw_F_12948 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_21 pcw_F_12365 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_10 mos_M_12977 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_37 pcw_M_263195015 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_11 yrs_F_12289 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12890 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_19 yrs_F_12832 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12889 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12889 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12981 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
posterior (caudal) superior temporal cortex (area 22c)_10 mos_M_12977 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
inner SZ in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SZ in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SZ in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in posterior frontal cortex (motor cortex) Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in posterior frontal cortex (motor cortex) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
VZ in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
caudal (posterior) extramural migratory stream Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal (posterior) extramural migratory stream relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
ventral posterior inferior nucleus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in ventral posterior inferior nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
lateral posterior nucleus of thalamus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in lateral posterior nucleus of thalamus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer SZ in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in posterior parahippocampal cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in posterior parahippocampal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
posterior cortical nucleus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior cortical nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
ventral posterior medial nucleus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in ventral posterior medial nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
ventral posterior lateral nucleus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in ventral posterior lateral nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
posterior hypothalamic nucleus Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in posterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Cataract, posterior polar, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cataract, posterior polar, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness, congenital heart defects, and posterior embryotoxon Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Posterior polar cataract type 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Posterior polar cataract type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cataract, posterior polar, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, posterior polar, 4 from the curated CTD Gene-Disease Associations dataset. |
Cataract, posterior polar, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cataract, posterior polar, 3 from the curated CTD Gene-Disease Associations dataset. |
Ossification of the posterior longitudinal ligament of the spine Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ossification of the posterior longitudinal ligament of the spine from the curated CTD Gene-Disease Associations dataset. |
Posterior column ataxia with retinitis pigmentosa Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Posterior column ataxia with retinitis pigmentosa from the curated CTD Gene-Disease Associations dataset. |
Posterior Leukoencephalopathy Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Posterior Leukoencephalopathy Syndrome from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Posterior Polymorphous, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 2 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Posterior Polymorphous, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 1 from the curated CTD Gene-Disease Associations dataset. |
Corneal Dystrophy, Posterior Polymorphous, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Corneal Dystrophy, Posterior Polymorphous, 3 from the curated CTD Gene-Disease Associations dataset. |
degeneration of macula and posterior pole Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease degeneration of macula and posterior pole from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
posterior uveal melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease posterior uveal melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
posterior scleritis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease posterior scleritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
degeneration of macula and posterior pole Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease degeneration of macula and posterior pole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
posterior cranial fossa meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease posterior cranial fossa meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
posterior polar cataract Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease posterior polar cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
posterior myocardial infarction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease posterior myocardial infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
posterior uveitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease posterior uveitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ossification of the posterior longitudinal ligament of the spine Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ossification of the posterior longitudinal ligament of the spine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
posterior cortical atrophy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease posterior cortical atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ossification of the posterior longitudinal ligament Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ossification of the posterior longitudinal ligament in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ossification of the posterior longitudinal ligament of the spine (opll) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ossification of the posterior longitudinal ligament of the spine (opll) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ossification of posterior longitudinal ligament; ossification, heterotopic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ossification of posterior longitudinal ligament; ossification, heterotopic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; ossification of posterior longitudinal ligament Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; ossification of posterior longitudinal ligament in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperostosis; ossification of posterior longitudinal ligament; spondylitis, ankylosing; uveitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperostosis; ossification of posterior longitudinal ligament; spondylitis, ankylosing; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
posterior urethral valves Gene SetFrom GAD Gene-Disease Associations genes associated with the disease posterior urethral valves in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ossification of posterior longitudinal ligament Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ossification of posterior longitudinal ligament in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
posterior Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term posterior in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
RALDH2_KO_GSE43578_6_mouse_head (rostral or posterior) Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the RALDH2_KO_GSE43578_6_mouse_head (rostral or posterior) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
embryonic heart tube anterior/posterior pattern specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
anterior/posterior axis specification, embryo Gene SetFrom GO Biological Process Annotations 2015 genes participating in the anterior/posterior axis specification, embryo biological process from the curated GO Biological Process Annotations 2015 dataset. |
specification of ureteric bud anterior/posterior symmetry Gene SetFrom GO Biological Process Annotations 2015 genes participating in the specification of ureteric bud anterior/posterior symmetry biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
posterior compartment specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the posterior compartment specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
anterior/posterior pattern specification involved in kidney development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations 2015 dataset. |
canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
specification of posterior mesonephric tubule identity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the specification of posterior mesonephric tubule identity biological process from the curated GO Biological Process Annotations 2015 dataset. |
anterior/posterior pattern specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
polarity specification of anterior/posterior axis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the polarity specification of anterior/posterior axis biological process from the curated GO Biological Process Annotations 2015 dataset. |
epiblast cell-extraembryonic ectoderm cell signaling involved in anterior/posterior axis specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the epiblast cell-extraembryonic ectoderm cell signaling involved in anterior/posterior axis specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
zygotic determination of anterior/posterior axis, embryo Gene SetFrom GO Biological Process Annotations 2015 genes participating in the zygotic determination of anterior/posterior axis, embryo biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
posterior mesonephric tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the posterior mesonephric tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
anterior/posterior axis specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the anterior/posterior axis specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
neural plate anterior/posterior regionalization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the neural plate anterior/posterior regionalization biological process from the curated GO Biological Process Annotations 2015 dataset. |
spinal cord anterior/posterior patterning Gene SetFrom GO Biological Process Annotations 2015 genes participating in the spinal cord anterior/posterior patterning biological process from the curated GO Biological Process Annotations 2015 dataset. |
posterior midgut development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the posterior midgut development biological process from the curated GO Biological Process Annotations 2015 dataset. |
anterior/posterior axon guidance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the anterior/posterior axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset. |
anterior/posterior pattern specification involved in ureteric bud development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the anterior/posterior pattern specification involved in ureteric bud development biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
forebrain anterior/posterior pattern specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the forebrain anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
specification of ureteric bud anterior/posterior symmetry by bmp signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the specification of ureteric bud anterior/posterior symmetry by bmp signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of transcription involved in anterior/posterior axis specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of transcription involved in anterior/posterior axis specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
degeneration of macula and posterior pole Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease degeneration of macula and posterior pole in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
polymorphous posterior corneal dystrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the polymorphous posterior corneal dystrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior lenticonus Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior lenticonus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased cervical spine flexion due to contractures of posterior cervical muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior subcapsular cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior vertebral hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior vertebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
iridescent posterior subcapsular cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the iridescent posterior subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior cortical cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia cutis congenita over posterior parietal area Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia cutis congenita over posterior parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior rib fusion Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior rib fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior polar cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
polymicrogyria, anterior to posterior gradient Gene SetFrom HPO Gene-Disease Associations genes associated with the polymicrogyria, anterior to posterior gradient phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior y-sutural cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior y-sutural cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
widened posterior fossa Gene SetFrom HPO Gene-Disease Associations genes associated with the widened posterior fossa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large posterior fontanelle Gene SetFrom HPO Gene-Disease Associations genes associated with the large posterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior choanal atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior choanal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
juvenile posterior subcapsular lenticular opacities Gene SetFrom HPO Gene-Disease Associations genes associated with the juvenile posterior subcapsular lenticular opacities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
midline skin dimples over anterior/posterior fontanelles Gene SetFrom HPO Gene-Disease Associations genes associated with the midline skin dimples over anterior/posterior fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior pituitary dysgenesis Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior pituitary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior plagiocephaly Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior plagiocephaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior scalloping of vertebral bodies Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior scalloping of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior wedging of vertebral bodies Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior wedging of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital posterior urethral valve Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital posterior urethral valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dense posterior cortical cataract Gene SetFrom HPO Gene-Disease Associations genes associated with the dense posterior cortical cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior embryotoxon Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior embryotoxon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior pharyngeal cleft Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior pharyngeal cleft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
spinal cord posterior columns myelin loss Gene SetFrom HPO Gene-Disease Associations genes associated with the spinal cord posterior columns myelin loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior leukoencephalopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior leukoencephalopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior fossa cyst Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior fossa cyst phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hump-shaped mound of bone in central and posterior portions of vertebral endplate Gene SetFrom HPO Gene-Disease Associations genes associated with the hump-shaped mound of bone in central and posterior portions of vertebral endplate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ectopic posterior pituitary Gene SetFrom HPO Gene-Disease Associations genes associated with the ectopic posterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior rib cupping Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior rib cupping phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neovascularization of peripheral and posterior retina Gene SetFrom HPO Gene-Disease Associations genes associated with the neovascularization of peripheral and posterior retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
white mater abnormalities in the posterior periventricular region Gene SetFrom HPO Gene-Disease Associations genes associated with the white mater abnormalities in the posterior periventricular region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Posterior Tibial Tendon Dysfunction Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Posterior Tibial Tendon Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Uveitis, Posterior Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Uveitis, Posterior phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Ossification of Posterior Longitudinal Ligament Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Ossification of Posterior Longitudinal Ligament phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
abnormal posterior definitive endoderm morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior definitive endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior cardinal vein morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior cardinal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum posterior vermis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum posterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior primitive streak morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior primitive streak morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior stroma morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior stroma morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye posterior chamber morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye posterior chamber morphology 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. |
abnormal left posterior bundle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal left posterior bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
posterior subcapsular cataracts Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the posterior subcapsular cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent posterior semicircular canal Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent posterior semicircular canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum posterior lobe morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum posterior lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated posterior semicircular canal Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated posterior semicircular canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal anterior commissure pars posterior morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal anterior commissure pars posterior morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior semicircular canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior semicircular canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior eye segment morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
posterior microphthalmia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the posterior microphthalmia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
microcornea, rod-cone dystrophy, cataract, and posterior staphyloma Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcornea, rod-cone dystrophy, cataract, and posterior staphyloma phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, posterior polymorphous, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, posterior polymorphous, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ataxia, posterior column, with retinitis pigmentosa Gene SetFrom OMIM Gene-Disease Associations genes associated with the ataxia, posterior column, with retinitis pigmentosa phenotype from the curated OMIM Gene-Disease Associations dataset. |
deafness, congenital heart defects, and posterior embryotoxon Gene SetFrom OMIM Gene-Disease Associations genes associated with the deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated OMIM Gene-Disease Associations dataset. |
corneal dystrophy, posterior polymorphous 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the corneal dystrophy, posterior polymorphous 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
posterior nuclear complex of thalamus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior nuclear complex of thalamus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ventral posterior nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ventral posterior nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior silk gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior silk gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior lobe Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
tibialis posterior Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue tibialis posterior in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior hypothalamic nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior cardinal vein Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior cardinal vein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior cingulate cortex Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior cingulate cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior adductor muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior adductor muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
ventral posterior inferior nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ventral posterior inferior nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
lateral posterior nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue lateral posterior nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior periventricular nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior periventricular nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior pharynx Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior pharynx in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior midgut Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior midgut in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior amygdala Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior amygdala in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior spinal root Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior paraventricular nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior paraventricular nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
posterior olfactory lobule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue posterior olfactory lobule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Posterior Subcapsular Cataract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Posterior Urethral Valves Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Posterior Urethral Valves in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Uveitis, Posterior Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uveitis, Posterior in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Capsule Opacification Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Capsule Opacification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Circulation Transient Ischemic Attack Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Circulation Transient Ischemic Attack in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Fossa Meningioma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Fossa Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Reversible Encephalopathy Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Reversible Encephalopathy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Synostotic Posterior Plagiocephaly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Synostotic Posterior Plagiocephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Cutis Congenita Over Posterior Parietal Area Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita Over Posterior Parietal Area in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, And Posterior Staphyloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Microcornea, Rod-Cone Dystrophy, Cataract, Posterior Staphyloma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Embryotoxon Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Embryotoxon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Synechiae Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Synechiae in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ossification Of The Posterior Longitudinal Ligament Of Spine Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ossification Of The Posterior Longitudinal Ligament Of Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Crossbite Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Crossbite in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Retinal Neovascularization Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Retinal Neovascularization in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Rib Gap Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Rib Gap in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Vitreous Detachment Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Vitreous Detachment in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Posterior Polar Cataract Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Posterior Polar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Cortical Atrophy Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Cortical Atrophy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Fossa Compression Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Fossa Compression Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Plagiocephaly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Plagiocephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Tibial Tendon Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Tibial Tendon Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Column Ataxia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Column Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Column Ataxia With Retinitis Pigmentosa Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Column Ataxia With Retinitis Pigmentosa in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Ischemic Optic Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Ischemic Optic Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Lenticonus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Lenticonus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Left Posterior Fascicular Block Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Left Posterior Fascicular Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Malignant Tumor Of Posterior Wall Of Nasopharynx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Malignant Tumor Of Posterior Wall Of Nasopharynx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neoplasm Of The Posterior Pituitary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neoplasm Of The Posterior Pituitary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acute Posterior Multifocal Placoid Pigment Epitheliopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Posterior Multifocal Placoid Pigment Epitheliopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ectopic Posterior Pituitary Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ectopic Posterior Pituitary Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Leukoencephalopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Leukoencephalopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Leukoencephalopathy Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Leukoencephalopathy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Fossa Cyst Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Fossa Cyst in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Widened Posterior Fossa Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widened Posterior Fossa in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Choroidal Artery Infarction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Choroidal Artery Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Polar Cataract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Polar Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ectopic Posterior Pituitary Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ectopic Posterior Pituitary in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Spinal Cord Posterior Columns Myelin Loss Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Spinal Cord Posterior Columns Myelin Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Rib Cupping Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Rib Cupping in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Pharyngeal Cleft Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Pharyngeal Cleft in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Helix Pit Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Helix Pit in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Iridescent Posterior Subcapsular Cataract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Iridescent Posterior Subcapsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Vertebral Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Vertebral Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Capsular Cataract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Capsular Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Y-Sutural Cataract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Y-Sutural Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Brain Infarction, Posterior Circulation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Brain Infarction, Posterior Circulation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Small Posterior Fossa Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Posterior Fossa in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Myocardial Infarction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Myocardial Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Cervical Spine Flexion Due To Contractures Of Posterior Cervical Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Fossa Hemorrhage Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Fossa Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Posterior Fontanelle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Posterior Fontanelle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Open Bite Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Open Bite in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Scalloping Of Vertebral Bodies Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Scalloping Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Cerebral Artery Occlusion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Cerebral Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
White Mater Abnormalities In The Posterior Periventricular Region Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Mater Abnormalities In The Posterior Periventricular Region in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Juvenile Posterior Subcapsular Lenticular Opacities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Juvenile Posterior Subcapsular Lenticular Opacities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dense Posterior Cortical Cataract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dense Posterior Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Cortical Cataract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Cortical Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Low Back Pain, Posterior Compartment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Low Back Pain, Posterior Compartment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Electrocardiogram Left Posterior Hemiblock (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Electrocardiogram Left Posterior Hemiblock (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Wedging Of Vertebral Bodies Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Wedging Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Premature Posterior Fontanelle Closure Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Posterior Fontanelle Closure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Posterior Rib Fusion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Posterior Rib Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hump-Shaped Mound Of Bone In Central And Posterior Portions Of Vertebral Endplate Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hump-Shaped Mound Of Bone In Central And Posterior Portions Of Vertebral Endplate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Midline Skin Dimples Over Anterior/Posterior Fontanelles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Midline Skin Dimples Over Anterior/Posterior Fontanelles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
anterior/posterior axis specification, embryo Gene SetFrom GO Biological Process Annotations 2023 genes participating in the anterior/posterior axis specification, embryo biological process from the curated GO Biological Process Annotations 2023 dataset. |
anterior/posterior pattern specification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2023 dataset. |
anterior/posterior axis specification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the anterior/posterior axis specification biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of canonical Wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of canonical Wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
embryonic heart tube anterior/posterior pattern specification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2023 dataset. |
specification of ureteric bud anterior/posterior symmetry by BMP signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the specification of ureteric bud anterior/posterior symmetry by BMP signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
posterior mesonephric tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the posterior mesonephric tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
posterior compartment specification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the posterior compartment specification biological process from the curated GO Biological Process Annotations 2023 dataset. |
dorsal spinal cord interneuron posterior axon guidance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the dorsal spinal cord interneuron posterior axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset. |
fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
polarity specification of anterior/posterior axis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the polarity specification of anterior/posterior axis biological process from the curated GO Biological Process Annotations 2023 dataset. |
posterior lateral line neuromast hair cell development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the posterior lateral line neuromast hair cell development biological process from the curated GO Biological Process Annotations 2023 dataset. |
specification of posterior mesonephric tubule identity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the specification of posterior mesonephric tubule identity biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
neural plate anterior/posterior regionalization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the neural plate anterior/posterior regionalization biological process from the curated GO Biological Process Annotations 2023 dataset. |
anterior/posterior axon guidance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the anterior/posterior axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of canonical Wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of canonical Wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
specification of ureteric bud anterior/posterior symmetry Gene SetFrom GO Biological Process Annotations 2023 genes participating in the specification of ureteric bud anterior/posterior symmetry biological process from the curated GO Biological Process Annotations 2023 dataset. |
zygotic determination of anterior/posterior axis, embryo Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zygotic determination of anterior/posterior axis, embryo biological process from the curated GO Biological Process Annotations 2023 dataset. |
posterior lateral line neuromast hair cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the posterior lateral line neuromast hair cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
anterior/posterior pattern specification involved in kidney development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal posterior primitive streak morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal posterior primitive streak morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent posterior semicircular canal Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent posterior semicircular canal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal posterior semicircular canal morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal posterior semicircular canal morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal anterior commissure pars posterior morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal anterior commissure pars posterior morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cerebellum posterior vermis morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellum posterior vermis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal left posterior bundle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal left posterior bundle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
posterior subcapsular cataract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the posterior subcapsular cataract 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. |
abnormal cornea posterior stroma morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cornea posterior stroma morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye posterior chamber morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye posterior chamber morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal digastric posterior belly morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal digastric posterior belly morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal posterior eye segment morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal posterior eye segment morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal posterior cardinal vein morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal posterior cardinal vein morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated posterior semicircular canal Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated posterior semicircular canal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal stapes posterior crus morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal stapes posterior crus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal posterior longitudinal ligament morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal posterior longitudinal ligament morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
large posterior fontanelle Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the large posterior fontanelle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
posterior cortical cataract Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the posterior cortical cataract phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal posterior definitive endoderm morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal posterior definitive endoderm morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal posterior cranial fossa morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal posterior cranial fossa morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
posterior microphthalmia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the posterior microphthalmia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent segment of posterior cerebral artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent segment of posterior cerebral artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent posterior communicating artery Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent posterior communicating artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent posterior commissure Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent posterior commissure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye posterior chamber depth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal eye posterior chamber depth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
posterior iris synechia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the posterior iris synechia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased heart left ventricle posterior wall thickness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased heart left ventricle posterior wall thickness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal eye posterior chamber depth Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal eye posterior chamber depth phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Oligodendrocyte_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Oligodendrocyte_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Ependymal cell_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Ependymal cell_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Neuron_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Neuron_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Vascular smooth muscle cell(VSMC)_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Vascular smooth muscle cell(VSMC)_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Pericyte_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Pericyte_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Histaminergic neuron_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Histaminergic neuron_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Astrocyte_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Astrocyte_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Vascular endothelial cell_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Vascular endothelial cell_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
GABAergic neuron_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the GABAergic neuron_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Macrophage_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Macrophage_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Vascular leptomeningeal cell_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Vascular leptomeningeal cell_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Tanycyte_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Tanycyte_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Microglial cell_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Microglial cell_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Glutamatergic neuron_Ventral posterior hypothalamus (VPH)_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Glutamatergic neuron_Ventral posterior hypothalamus (VPH)_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Posterior presomitic mesoderm(pPSM) cell_Posterior presomitic mesoderm_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Posterior presomitic mesoderm(pPSM) cell_Posterior presomitic mesoderm_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Posterior hindbrain cell_Embryo_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Posterior hindbrain cell_Embryo_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Posterior second heart field(pSHF) cell_Posterior second heart field_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Posterior second heart field(pSHF) cell_Posterior second heart field_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Posterior foregut cell_Intestine_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Posterior foregut cell_Intestine_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Posterior placode cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Posterior placode cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Posterior cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Posterior cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Epidermal posterior cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Epidermal posterior cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Formation of the posterior neural plate Gene Setproteins participating in the Formation of the posterior neural plate pathway from the Reactome Pathways 2024 dataset. |
anterior/posterior axis specification, embryo Gene SetFrom GO Biological Process Annotations 2025 genes participating in the anterior/posterior axis specification, embryo biological process from the curated GO Biological Process Annotations 2025 dataset. |
anterior/posterior pattern specification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2025 dataset. |
anterior/posterior axis specification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the anterior/posterior axis specification biological process from the curated GO Biological Process Annotations 2025 dataset. |
neural plate anterior/posterior regionalization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the neural plate anterior/posterior regionalization biological process from the curated GO Biological Process Annotations 2025 dataset. |
embryonic heart tube anterior/posterior pattern specification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations 2025 dataset. |
posterior mesonephric tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the posterior mesonephric tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
posterior compartment specification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the posterior compartment specification biological process from the curated GO Biological Process Annotations 2025 dataset. |
dorsal spinal cord interneuron posterior axon guidance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the dorsal spinal cord interneuron posterior axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset. |
polarity specification of anterior/posterior axis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the polarity specification of anterior/posterior axis biological process from the curated GO Biological Process Annotations 2025 dataset. |
posterior lateral line neuromast hair cell development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the posterior lateral line neuromast hair cell development biological process from the curated GO Biological Process Annotations 2025 dataset. |
specification of posterior mesonephric tubule identity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the specification of posterior mesonephric tubule identity biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
anterior/posterior axon guidance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the anterior/posterior axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset. |
zygotic determination of anterior/posterior axis, embryo Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zygotic determination of anterior/posterior axis, embryo biological process from the curated GO Biological Process Annotations 2025 dataset. |
posterior lateral line neuromast hair cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the posterior lateral line neuromast hair cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
anterior/posterior pattern specification involved in kidney development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Degeneration of macula and posterior pole Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Degeneration of macula and posterior pole from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Degeneration of macula and posterior pole Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Degeneration of macula and posterior pole in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ossification of the posterior longitudinal ligament of spine Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Ossification of the posterior longitudinal ligament of spine in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ossification of the posterior longitudinal ligament of spine Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ossification of the posterior longitudinal ligament of spine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Degeneration of macula and posterior pole Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Degeneration of macula and posterior pole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polar cataract Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polar cataract in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior fossa meningioma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior fossa meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior scleritis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior scleritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior uveitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior uveitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior fossa ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior fossa ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polymorphous corneal dystrophy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polymorphous corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior amorphous corneal dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior amorphous corneal dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polymorphous corneal dystrophy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior myocardial infarction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior myocardial infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior uveal melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior uveal melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior pituitary gland neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior pituitary gland neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior fossa group B ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior fossa group B ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior fossa group A ependymoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior fossa group A ependymoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior cerebral artery infarction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior cerebral artery infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polymorphous corneal dystrophy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior dislocation of lens Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior dislocation of lens in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior polymorphous corneal dystrophy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Posterior polymorphous corneal dystrophy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Posterior midgut Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior midgut in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior cingulate cortex Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior cingulate cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior silk gland Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior silk gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior lobe Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior cardinal vein Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior cardinal vein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior nuclear complex of thalamus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior nuclear complex of thalamus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior hypothalamic nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Lateral posterior nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Lateral posterior nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ventral posterior nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ventral posterior nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior paraventricular nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior paraventricular nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior adductor muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior adductor muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Tibialis posterior Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Tibialis posterior in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Ventral posterior inferior nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ventral posterior inferior nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior amygdala Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior amygdala in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior olfactory lobule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior olfactory lobule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior periventricular nucleus Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior periventricular nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior pharynx Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior pharynx in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior chamber of the eye Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior spinal root Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Posterior spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Posterior cell cortex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Posterior cell cortex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Posterior column ataxia-retinitis pigmentosa syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Posterior column ataxia-retinitis pigmentosa syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Posterior polymorphous corneal dystrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Posterior polymorphous corneal dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lymphedema-posterior choanal atresia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lymphedema-posterior choanal atresia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Posterior cortical atrophy and Alzheimer's disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Posterior cortical atrophy and Alzheimer's disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
White matter microstructure in first episode schizophrenia (right posterior cingulate cortex) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter microstructure in first episode schizophrenia (right posterior cingulate cortex) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
White matter microstructure in first episode schizophrenia (left posterior cingulate cortex) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the White matter microstructure in first episode schizophrenia (left posterior cingulate cortex) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Ossification of the posterior longitudinal ligament of the spine Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ossification of the posterior longitudinal ligament of the spine phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Posterior-cingulate cortex volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Posterior-cingulate cortex volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corpus callosum posterior volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corpus callosum posterior volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Corpus callosum Mid-posterior volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corpus callosum Mid-posterior volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Decline in glucose metabolism in posterior cingulate cortex Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Decline in glucose metabolism in posterior cingulate cortex phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Posterior thalamic nuclei volume Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Posterior thalamic nuclei volume 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 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 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 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 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. |
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. |
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 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 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 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 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 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 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. |