Name

posterior vertebral hypoplasia Gene Set

From 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.

posterior scalloping of vertebral bodies Gene Set

From 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 Set

From 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.

hump-shaped mound of bone in central and posterior portions of vertebral endplate Gene Set

From 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.

aplasia/hypoplasia involving the vertebral column Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral body hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vertebral body hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Sacral agenesis with vertebral anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sacral agenesis with vertebral anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

vertebral artery insufficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease vertebral artery insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

vertebral artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease vertebral artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bone density; fractures, vertebral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fractures, vertebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vertebral artery dissection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vertebral artery dissection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vertebral fracture Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vertebral fracture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

prevalent vertebral fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease prevalent vertebral fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vertebral Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term vertebral in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

abnormality of the vertebral column Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

vertebral body sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the vertebral body sclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the curvature of the vertebral column Gene Set

From 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.

butterfly vertebral arch Gene Set

From HPO Gene-Disease Associations

genes associated with the butterfly vertebral arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sclerotic vertebral endplates Gene Set

From HPO Gene-Disease Associations

genes associated with the sclerotic vertebral endplates phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cervical vertebral fusion (c2/c3) Gene Set

From HPO Gene-Disease Associations

genes associated with the cervical vertebral fusion (c2/c3) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent or minimally ossified vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the absent or minimally ossified vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral hyperostosis Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral hyperostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

narrow vertebral interpedicular distance Gene Set

From HPO Gene-Disease Associations

genes associated with the narrow vertebral interpedicular distance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral arch anomaly Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral arch anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cleft vertebral arch Gene Set

From HPO Gene-Disease Associations

genes associated with the cleft vertebral arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

c1-c2 vertebral abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the c1-c2 vertebral abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vertebral pedicle morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vertebral pedicle morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cuboid-shaped vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the cuboid-shaped vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior clefting of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior clefting of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

biconcave vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the biconcave vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple small vertebral fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple small vertebral fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

small cervical vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the small cervical vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral compression fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral compression fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

irregular vertebral endplates Gene Set

From HPO Gene-Disease Associations

genes associated with the irregular vertebral endplates phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral body sclerosis Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral body sclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

beaking of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the beaking of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tall lumbar vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the tall lumbar vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vertebral segmentation and fusion Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vertebral segmentation and fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

beaking of vertebral bodies t12-l3 Gene Set

From HPO Gene-Disease Associations

genes associated with the beaking of vertebral bodies t12-l3 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral clefting Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral clefting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the curvature of the vertebral column Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the curvature of the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sandwich appearance of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the sandwich appearance of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal form of the vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

enlarged vertebral pedicles Gene Set

From HPO Gene-Disease Associations

genes associated with the enlarged vertebral pedicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplastic vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplastic vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral fusion Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vertebral ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vertebral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the vertebral spinous processes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vertebral spinous processes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent in utero ossification of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the absent in utero ossification of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disc-like vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the disc-like vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent vertebral body mineralization Gene Set

From HPO Gene-Disease Associations

genes associated with the absent vertebral body mineralization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

unossified vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the unossified vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior rounding of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior rounding of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

supernumerary vertebral ossification centers Gene Set

From HPO Gene-Disease Associations

genes associated with the supernumerary vertebral ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the vertebral endplates Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vertebral endplates phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased vertebral height Gene Set

From HPO Gene-Disease Associations

genes associated with the increased vertebral height phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ovoid vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the ovoid vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral wedging Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral wedging phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive cervical vertebral spine fusion Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive cervical vertebral spine fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of vertebral epiphysis morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of vertebral epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

scheuermann-like vertebral changes Gene Set

From HPO Gene-Disease Associations

genes associated with the scheuermann-like vertebral changes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

punctate vertebral calcifications Gene Set

From HPO Gene-Disease Associations

genes associated with the punctate vertebral calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the vertebral column Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Vertebral Artery Dissection Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Vertebral Artery Dissection phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

asymmetric rib-vertebral column attachment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the asymmetric rib-vertebral column attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral lamina morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral lamina morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral arch morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

caudal vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the caudal vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fusion of vertebral arches Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fusion of vertebral arches phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cervical vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cervical vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral spinous process Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral spinous process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short vertebral body Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lumbar vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lumbar vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral pedicle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral pedicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral arch Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral artery morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral articular process morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral articular process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thoracic vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thoracic vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sacral vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sacral vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral column morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral body Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral epiphyseal plate morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral epiphyseal plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged vertebral body Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral spinous process morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral spinous process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral pedicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral pedicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cervical vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cervical vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vertebral compression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vertebral compression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fusion of vertebral bodies Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fusion of vertebral bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

elongated vertebral body Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the elongated vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal rib-vertebral column attachment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal rib-vertebral column attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral arch development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small vertebral body Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral transverse processes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral transverse processes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sacral vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sacral vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lumbar vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lumbar vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

caudal vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the caudal vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short vertebral column Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short vertebral column phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thoracic vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thoracic vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral body morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

elongated vertebral column Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the elongated vertebral column phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral body development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral body development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral transverse process morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral transverse process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sacral agenesis with vertebral anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the sacral agenesis with vertebral anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

vertebral ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue vertebral ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

paracentral lobule, posterior part, left, bank of cingulate sulcus Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From DISEASES Curated Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From DISEASES Text-mining Gene-Disease Assocation 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior axis specification, embryo Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior axis specification, embryo biological process from the curated GO Biological Process Annotations dataset.

specification of ureteric bud anterior/posterior symmetry Gene Set

From GO Biological Process Annotations

genes participating in the specification of ureteric bud anterior/posterior symmetry biological process from the curated GO Biological Process Annotations dataset.

negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

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 dataset.

posterior compartment specification Gene Set

From GO Biological Process Annotations

genes participating in the posterior compartment specification biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

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 dataset.

specification of posterior mesonephric tubule identity Gene Set

From GO Biological Process Annotations

genes participating in the specification of posterior mesonephric tubule identity biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

polarity specification of anterior/posterior axis Gene Set

From GO Biological Process Annotations

genes participating in the polarity specification of anterior/posterior axis biological process from the curated GO Biological Process Annotations dataset.

epiblast cell-extraembryonic ectoderm cell signaling involved in anterior/posterior axis specification Gene Set

From GO Biological Process Annotations

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 dataset.

zygotic determination of anterior/posterior axis, embryo Gene Set

From GO Biological Process Annotations

genes participating in the zygotic determination of anterior/posterior axis, embryo biological process from the curated GO Biological Process Annotations dataset.

regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

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 dataset.

posterior mesonephric tubule development Gene Set

From GO Biological Process Annotations

genes participating in the posterior mesonephric tubule development biological process from the curated GO Biological Process Annotations dataset.

negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

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 dataset.

anterior/posterior axis specification Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior axis specification biological process from the curated GO Biological Process Annotations dataset.

fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

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 dataset.

neural plate anterior/posterior regionalization Gene Set

From GO Biological Process Annotations

genes participating in the neural plate anterior/posterior regionalization biological process from the curated GO Biological Process Annotations dataset.

spinal cord anterior/posterior patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord anterior/posterior patterning biological process from the curated GO Biological Process Annotations dataset.

posterior midgut development Gene Set

From GO Biological Process Annotations

genes participating in the posterior midgut development biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior axon guidance biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification involved in ureteric bud development Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification involved in ureteric bud development biological process from the curated GO Biological Process Annotations dataset.

regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

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 dataset.

forebrain anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the forebrain anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

specification of ureteric bud anterior/posterior symmetry by bmp signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the specification of ureteric bud anterior/posterior symmetry by bmp signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription involved in anterior/posterior axis specification Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription involved in anterior/posterior axis specification biological process from the curated GO Biological Process Annotations dataset.

degeneration of macula and posterior pole Gene Set

From 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.

abnormality of the posterior segment of the eye Gene Set

From 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.

polymorphous posterior corneal dystrophy Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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.

abnormality of the posterior pituitary Gene Set

From 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.

iridescent posterior subcapsular cataract Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

abnormality of the posterior hairline Gene Set

From 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.

polymicrogyria, anterior to posterior gradient Gene Set

From 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 Set

From 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 Set

From 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.

low posterior hairline Gene Set

From 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.

large posterior fontanelle Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

congenital posterior urethral valve Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

abnormality of the posterior cranial fossa Gene Set

From 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.

posterior fossa cyst Gene Set

From 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.

ectopic posterior pituitary Gene Set

From 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 Set

From 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.

abnormality of the posterior segment of the eye Gene Set

From 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.

neovascularization of peripheral and posterior retina Gene Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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 Set

From 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.

Focal dermal hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Focal dermal hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and presenile cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tibia, hypoplasia of, with polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tibia, hypoplasia of, with polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hypoplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and anterior segment dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia, type 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 2D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic nerve hypoplasia, bilateral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic nerve hypoplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Splenic hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Splenic hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Olivopontocerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Olivopontocerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia, type 1b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia, type 1b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia, type 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia type 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pontocerebellar hypoplasia, type 2e Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pontocerebellar hypoplasia, type 2e phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Focal Dermal Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Focal Dermal Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Fibular hypoplasia and complex brachydactyly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset.

Cartilage-hair hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cartilage-hair hypoplasia from the curated CTD Gene-Disease Associations dataset.

Leydig Cell Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leydig Cell Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Optic Nerve Hypoplasia, Bilateral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic Nerve Hypoplasia, Bilateral from the curated CTD Gene-Disease Associations dataset.

Polymicrogyria With Optic Nerve Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polymicrogyria With Optic Nerve Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2C from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2B from the curated CTD Gene-Disease Associations dataset.

ADRENAL HYPOPLASIA, CONGENITAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ADRENAL HYPOPLASIA, CONGENITAL from the curated CTD Gene-Disease Associations dataset.

Anophthalmia with pulmonary hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anophthalmia with pulmonary hypoplasia from the curated CTD Gene-Disease Associations dataset.

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 6 from the curated CTD Gene-Disease Associations dataset.

PONTOCEREBELLAR HYPOPLASIA, TYPE 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PONTOCEREBELLAR HYPOPLASIA, TYPE 4 from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 1 from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 3 from the curated CTD Gene-Disease Associations dataset.

Iris hypoplasia and glaucoma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset.

Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset.

Pontocerebellar Hypoplasia Type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2A from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset.

Foveal Hypoplasia and Anterior Segment Dysgenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Foveal Hypoplasia and Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset.

focal dermal hypoplasia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease focal dermal hypoplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

dental enamel hypoplasia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease dental enamel hypoplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

focal dermal hypoplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease focal dermal hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cartilage-hair hypoplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cartilage-hair hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pituitary hypoplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease pituitary hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

dental enamel hypoplasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease dental enamel hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypoplasia Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term hypoplasia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Primary pulmonary hypoplasia_Lung Tissue_GSE1363 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Primary pulmonary hypoplasia_Lung Tissue_GSE1363 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

aplasia/hypoplasia involving the central nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

aplasia/hypoplasia of the cerebrum Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the aplasia/hypoplasia of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

retinal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the retinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of choroid Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the fallopian tube Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of lymphatic vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the uvula Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the uvula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tragus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the tragus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the nose Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the frontal sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

parathyroid hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the parathyroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the lungs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the lungs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pancreatic hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the pancreatic hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the quadriceps Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the quadriceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the musculature of the upper arm Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the scapulae Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the scapulae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the ventral pons Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the ventral pons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

glenoid fossa hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the glenoid fossa hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lymph node hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the lymph node hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of toe Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the iris Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the lacrimal puncta Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the lacrimal puncta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the pyramidal tract Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving forearm bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving forearm bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the nasal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the sternum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the optic nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the ovary Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the corticospinal tracts Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of penis Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of penis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic disc hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the optic disc hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tarsal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the thymus Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thyroid hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the thyroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the ulna Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the feet Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the primary teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the biceps Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the biceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the fundus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the fundus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the retina Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the odontoid process Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

calf muscle hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the calf muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the gallbladder Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the gallbladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the pelvis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the mandible Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the epiglottis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of metatarsal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of metatarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the uterus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

erythroid hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the erythroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the eyebrow Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the pons Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the pons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the spleen Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

breast hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the breast hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the choroid Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the ciliary body Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the ciliary body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the corpus callosum Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulmonary hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the pulmonary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the lower limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the brainstem Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the bladder Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the triceps Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the triceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the pharynx Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the pharynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

macular hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the macular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pectoralis hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the pectoralis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midclavicular hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the midclavicular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal hypoplasia/aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the renal hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the femoral head Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mandibular condyle hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the mandibular condyle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting bones of the axial skeleton Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting bones of the axial skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

corticospinal tract hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the corticospinal tract hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 1st metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

carpal bone hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the carpal bone hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal ulnar hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the distal ulnar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the earlobes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the earlobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the calcaneus Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the calcaneus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 4th metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of fingers Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the radius Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of proximal fibula Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of proximal fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of deltoid muscle Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of deltoid muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the thymus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 2nd metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 2nd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the skeleton Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the renal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the ulna Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the uterus Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the humerus Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the palmar creases Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the maxilla Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the maxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the ribs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 1st metatarsal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 1st metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

laryngeal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the laryngeal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lacrimal gland hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the lacrimal gland hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

frontal bone hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the frontal bone hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the metacarpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nipples Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nipples phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 5th metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the capital femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the proximal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the proximal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the diaphragm Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the premaxilla Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cerebrum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 3rd toe Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the bladder Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the uvea Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the uvea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the sweat glands Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

unilateral breast hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the unilateral breast hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thoracic hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the thoracic hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the femur Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pectoralis major hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the pectoralis major hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adrenal medullary hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the adrenal medullary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nasal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the testes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the testes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

labial hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the labial hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the thorax Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the maxilla Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the maxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the optic tract Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nails Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the corpus callosum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inferior vermis hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the inferior vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the brainstem Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the abdominal wall musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the fovea Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the fovea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cochlea Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the semicircular canal Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the semicircular canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the femoral head and neck Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the ear cartilage Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the ear cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

external genital hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the external genital hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the vagina Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of first ribs Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of first ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar hemisphere hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar hemisphere hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gonadal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the gonadal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the iris Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the extremities Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the nasal septum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

2nd-5th toe middle phalangeal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the 2nd-5th toe middle phalangeal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the clavicles Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the clavicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar vermis hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the sacrum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the sacrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adrenocortical hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the adrenocortical hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving bones of the skull Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the ovary Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the musculature of the pelvis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the musculature of the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized cerebral atrophy/hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tibia Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the tibia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the prostate Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the prostate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of proximal radius Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of proximal radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the patella Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the patella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the lesser trochanter Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the lesser trochanter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the skeletal musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the skeletal musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the central nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the eyelid Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the eyelid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the vagina Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

unilateral chest hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the unilateral chest hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the breasts Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the breasts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the musculature of the extremities Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the musculature of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

shoulder muscle hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the shoulder muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the pubic bone Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the pyramidal tract Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the pancreas Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebral hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the cochlea Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the fovea Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the fovea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

optic nerve hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the optic nerve hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cervical spine Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cervical spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cerebellum Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cerebellum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the carpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adrenal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the adrenal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hemifacial hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the hemifacial hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of dental enamel Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of dental enamel phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the lens Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the lens phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior pituitary hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior pituitary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the external ear Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the external ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the shoulder musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the shoulder musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the frontal lobes Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the frontal lobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

scrotal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the scrotal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the radius Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the capital femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the musculature of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the fallopian tube Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the tongue Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the tongue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

upper limb muscle hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the upper limb muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patellar hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the patellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the epiglottis Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the colon Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the colon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fibular hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the fibular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the 3rd metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pectoral muscle hypoplasia/aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the pectoral muscle hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pulmonary artery hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the pulmonary artery hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the macula Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the macula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplasia of the abdominal wall musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paranasal sinus hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the paranasal sinus hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

clitoral hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the clitoral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the musculature of the thigh Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the musculature of the thigh phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the phalanges of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the fibula Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

olivopontocerebellar hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the olivopontocerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

axillary apocrine gland hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the axillary apocrine gland hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Dental Enamel Hypoplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Dental Enamel Hypoplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

testis hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the testis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

tongue hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the tongue hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

genital tubercle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the genital tubercle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lymphoid hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lymphoid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

palatine bone horizontal plate hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the palatine bone horizontal plate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thyroid hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thyroid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hindbrain hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hindbrain hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

midface hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the midface hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intervertebral disk hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the intervertebral disk hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lymph node hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lymph node hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aortic arch hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aortic arch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pituitary intermediate lobe hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pituitary intermediate lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

temporal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the temporal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

iris stroma hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the iris stroma hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ischium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ischium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

oviduct hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the oviduct hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

spleen hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the spleen hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

radius hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the radius hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

otic vesicle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the otic vesicle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

malleus hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the malleus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

maxilla hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the maxilla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

uterine cervix hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the uterine cervix hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

adrenal gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the adrenal gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

palatal shelf hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the palatal shelf hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricle myocardium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricle myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

leydig cell hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the leydig cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

mammary gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the mammary gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

scrotum hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the scrotum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

diencephalon hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the diencephalon hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cochlear ganglion hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cochlear ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

frontal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the frontal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

head mesenchyme hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the head mesenchyme hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

myometrium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the myometrium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

papillary muscle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the papillary muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cerebellum vermis hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cerebellum vermis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sebaceous gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sebaceous gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premaxilla hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premaxilla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrium myocardium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrium myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pulmonary hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pulmonary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

female preputial gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the female preputial gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pharyngeal arch artery hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

epididymis hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the epididymis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

parathyroid hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the parathyroid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

olfactory bulb hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the olfactory bulb hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aorta hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aorta hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

heart hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ethmoturbinate hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ethmoturbinate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hyoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hyoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pituitary gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pituitary gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

parietal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the parietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

axial mesoderm hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the axial mesoderm hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

mesangial cell hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the mesangial cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

liver hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the liver hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

palatine bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the palatine bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pancreas hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pancreas hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

gonial bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the gonial bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ear lobe hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ear lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

conotruncal ridge hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the conotruncal ridge hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

adenohypophysis hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the adenohypophysis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

renal hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the renal hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

alisphenoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the alisphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vascular smooth muscle cell hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vascular smooth muscle cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hypaxial muscle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hypaxial muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

basisphenoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the basisphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pterygoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pterygoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

endometrium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the endometrium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vagina hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vagina hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

dorsal root ganglion hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the dorsal root ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aorta tubular hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aorta tubular hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

metacarpal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the metacarpal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

axial skeleton hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the axial skeleton hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

submandibular gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the submandibular gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

myocardial trabeculae hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the myocardial trabeculae hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vas deferens hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vas deferens hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cerebellum hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cerebellum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sinus venosus hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sinus venosus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

kidney medulla hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the kidney medulla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pubis hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pubis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ascending aorta hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ascending aorta hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

mandible hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the mandible hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

midbrain hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the midbrain hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

nasal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the nasal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

kidney cortex hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the kidney cortex hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

maxillary shelf hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the maxillary shelf hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

rathke's pouch hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the rathke's pouch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

clavicle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the clavicle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sertoli cell hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sertoli cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

eyelid hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the eyelid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

turbinate hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the turbinate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pulmonary trunk hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pulmonary trunk hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pancreatic acinar hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pancreatic acinar hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vestibular ganglion hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vestibular ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

clitoris hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the clitoris hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

placental labyrinth hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the placental labyrinth hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pharyngeal arch hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pharyngeal arch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ovary hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ovary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

exocrine pancreas hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the exocrine pancreas hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ureter hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ureter hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

glossopharyngeal nerve hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the glossopharyngeal nerve hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

telencephalon hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the telencephalon hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

forebrain hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the forebrain hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

scapular bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the scapular bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pancreatic islet hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pancreatic islet hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

seminal vesicle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the seminal vesicle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pharynx hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pharynx hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

myocardium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

trachea hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the trachea hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thymus cortex hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thymus cortex hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

palate bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the palate bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular myocardium compact layer hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular myocardium compact layer hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

inner ear hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the inner ear hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vomer bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vomer bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

optic nerve hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the optic nerve hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

meibomian gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the meibomian gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

interparietal bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the interparietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

uterus hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the uterus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

esophagus hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the esophagus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

stomach hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the stomach hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lateral prostate gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lateral prostate gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrium hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

bulbourethral gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the bulbourethral gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

philtrum hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the philtrum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

presphenoid bone hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the presphenoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

skeletal muscle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the skeletal muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

heart right ventricle hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the heart right ventricle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

urinary bladder hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the urinary bladder hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

trabecula carnea hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the trabecula carnea hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

kidney papillary hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the kidney papillary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

gonadal ridge hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the gonadal ridge hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pulmonary artery hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the pulmonary artery hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sternum hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sternum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

otic capsule hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the otic capsule hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

retina hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the retina hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

prostate gland hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the prostate gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thymus hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thymus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

iris hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the iris hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 2e Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 2e phenotype from the curated OMIM Gene-Disease Associations dataset.

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

leydig cell hypoplasia with hypergonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the leydig cell hypoplasia with hypergonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

leydig cell hypoplasia with pseudohermaphroditism Gene Set

From OMIM Gene-Disease Associations

genes associated with the leydig cell hypoplasia with pseudohermaphroditism phenotype from the curated OMIM Gene-Disease Associations dataset.

hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

iris hypoplasia and glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the iris hypoplasia and glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated OMIM Gene-Disease Associations dataset.

mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

focal dermal hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the focal dermal hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 2c Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 2c phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 2b Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 2a Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 2d Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 2d phenotype from the curated OMIM Gene-Disease Associations dataset.

foveal hypoplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the foveal hypoplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic nerve hypoplasia and abnormalities of the central nervous system Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic nerve hypoplasia and abnormalities of the central nervous system phenotype from the curated OMIM Gene-Disease Associations dataset.

patella aplasia or hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the patella aplasia or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 1c Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 1c phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

renal hypoplasia, isolated Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal hypoplasia, isolated phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia, type 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

polymicrogyria with optic nerve hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the polymicrogyria with optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

?breasts and/or nipples, aplasia or hypoplasia of, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?breasts and/or nipples, aplasia or hypoplasia of, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

optic nerve hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the optic nerve hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

pontocerebellar hypoplasia type 1a Gene Set

From OMIM Gene-Disease Associations

genes associated with the pontocerebellar hypoplasia type 1a phenotype from the curated OMIM Gene-Disease Associations dataset.

cartilage-hair hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cartilage-hair hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis phenotype from the curated OMIM Gene-Disease Associations dataset.