Name

abnormality of the subungual region Gene Set

From HPO Gene-Disease Associations

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

subungual Gene Set

From GeneRIF Biological Term Annotations

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

subungual fibromas Gene Set

From HPO Gene-Disease Associations

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

subungual hyperkeratosis Gene Set

From HPO Gene-Disease Associations

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

subungual hyperkeratotic fragments Gene Set

From HPO Gene-Disease Associations

genes associated with the subungual hyperkeratotic fragments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the femoral neck or head region Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the femoral neck or head region Gene Set

From HPO Gene-Disease Associations

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

abnormality of the periorbital region Gene Set

From HPO Gene-Disease Associations

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

abnormality of the nasolabial region Gene Set

From HPO Gene-Disease Associations

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

abnormality of the periungual region Gene Set

From HPO Gene-Disease Associations

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

abnormality of the orbital region Gene Set

From HPO Gene-Disease Associations

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

abnormality of the ocular region Gene Set

From HPO Gene-Disease Associations

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

abnormality of periauricular region Gene Set

From HPO Gene-Disease Associations

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

regional abnormality of skin Gene Set

From HPO Gene-Disease Associations

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

lateral hypothalamic area, anterior region, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, anterior region, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, mammillary region, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, mammillary region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

preoptic region, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in preoptic region, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, anterior region, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, anterior region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, tuberal region, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, tuberal region, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

preoptic region, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in preoptic region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, mammillary region, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, mammillary region, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

pretectal region Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in pretectal region relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Periventricular region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Periventricular region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Basic cell groups and regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Retrohippocampal region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Retrohippocampal region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Hippocampal region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Hippocampal region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Vermal regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Vermal regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Hemispheric regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Hemispheric regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Pallidum, medial region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Pallidum, medial region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Pallidum, dorsal region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Pallidum, dorsal region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Pretectal region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Pretectal region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Striatum dorsal region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Striatum dorsal region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Pallidum, caudal region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Pallidum, caudal region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior olivary complex, periolivary region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior olivary complex, periolivary region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Pallidum, ventral region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Pallidum, ventral region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Striatum ventral region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Striatum ventral region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Cochlear nucleus, subpedunclular granular region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Cochlear nucleus, subpedunclular granular region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

LGE-VZ border region Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in LGE-VZ border region relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

VZ in septal region Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VZ in septal region relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

upper limb region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in upper limb region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

VZ in postamygdaloid region Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VZ in postamygdaloid region relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

head and face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

MGE-Lateral region Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in MGE-Lateral region relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

lower limb region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lower limb region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

VZ in subcallosal region Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VZ in subcallosal region relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

VZ in thalamic region Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in VZ in thalamic region relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

myelin sheath adaxonal region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the myelin sheath adaxonal region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chromosomal region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the chromosomal region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

nucleolus organizer region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the nucleolus organizer region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed chromosome, centromeric region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extracellular region part Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extracellular region part cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

internode region of axon Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the internode region of axon cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intracellular region of host Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intracellular region of host cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chromosome, centromeric region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

extracellular region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the extracellular region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

plasma membrane region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the plasma membrane region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

membrane region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the membrane region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

myelin sheath abaxonal region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the myelin sheath abaxonal region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

juxtaparanode region of axon Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the juxtaparanode region of axon cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

nuclear chromosome, telomeric region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the nuclear chromosome, telomeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

perinuclear region of cytoplasm Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the perinuclear region of cytoplasm cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

paranode region of axon Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the paranode region of axon cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chromosome, telomeric region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the chromosome, telomeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

condensed nuclear chromosome, centromeric region Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the condensed nuclear chromosome, centromeric region cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chromosomal region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chromosomal region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

nucleolus organizer region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nucleolus organizer region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed chromosome, centromeric region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

extracellular region part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the extracellular region part cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

chromosome, centromeric region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

extracellular region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the extracellular region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

plasma membrane region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the plasma membrane region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

dna replication termination region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the dna replication termination region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

membrane region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the membrane region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

juxtaparanode region of axon Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the juxtaparanode region of axon cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

nuclear chromosome, telomeric region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nuclear chromosome, telomeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

perinuclear region of cytoplasm Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the perinuclear region of cytoplasm cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

paranode region of axon Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the paranode region of axon cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

chromosome, telomeric region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chromosome, telomeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

condensed nuclear chromosome, centromeric region Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the condensed nuclear chromosome, centromeric region cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Williams-Beuren Region Duplication Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Williams-Beuren Region Duplication Syndrome from the curated CTD Gene-Disease Associations dataset.

pineal region teratoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pineal region choriocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

pineal region meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

complex regional pain syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease complex regional pain syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

complex regional pain syndromes; dystonia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complex regional pain syndromes; dystonia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

verbal learning, verbal memory, and regional cortical gray matter density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease verbal learning, verbal memory, and regional cortical gray matter density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

regional fat distribution Gene Set

From GAD Gene-Disease Associations

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

regional Gene Set

From GeneRIF Biological Term Annotations

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

regions Gene Set

From GeneRIF Biological Term Annotations

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

region1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term region1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

regionalization Gene Set

From GeneRIF Biological Term Annotations

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

regioncabl Gene Set

From GeneRIF Biological Term Annotations

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

regionspecific Gene Set

From GeneRIF Biological Term Annotations

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

regionally Gene Set

From GeneRIF Biological Term Annotations

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

regiondeficient Gene Set

From GeneRIF Biological Term Annotations

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

regiondependent Gene Set

From GeneRIF Biological Term Annotations

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

region Gene Set

From GeneRIF Biological Term Annotations

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

regionalized Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of transcription regulatory region dna binding Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of transcription regulatory region dna binding biological process from the curated GO Biological Process Annotations dataset.

regulation of rna polymerase ii regulatory region sequence-specific dna binding Gene Set

From GO Biological Process Annotations

genes participating in the regulation of rna polymerase ii regulatory region sequence-specific dna binding biological process from the curated GO Biological Process Annotations dataset.

protein localization to myelin sheath abaxonal region Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to myelin sheath abaxonal region biological process from the curated GO Biological Process Annotations dataset.

negative regulation of rna polymerase ii regulatory region sequence-specific dna binding Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of rna polymerase ii regulatory region sequence-specific dna binding biological process from the curated GO Biological Process Annotations dataset.

cerebral cortex regionalization Gene Set

From GO Biological Process Annotations

genes participating in the cerebral cortex regionalization biological process from the curated GO Biological Process Annotations dataset.

protein localization to chromosome, centromeric region Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to chromosome, centromeric region biological process from the curated GO Biological Process Annotations dataset.

neural plate mediolateral regionalization Gene Set

From GO Biological Process Annotations

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

positive regulation of transcription regulatory region dna binding Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of transcription regulatory region dna binding biological process from the curated GO Biological Process Annotations dataset.

regionalization Gene Set

From GO Biological Process Annotations

genes participating in the regionalization biological process from the curated GO Biological Process Annotations dataset.

telencephalon regionalization Gene Set

From GO Biological Process Annotations

genes participating in the telencephalon regionalization biological process from the curated GO Biological Process Annotations dataset.

establishment of protein localization to juxtaparanode region of axon Gene Set

From GO Biological Process Annotations

genes participating in the establishment of protein localization to juxtaparanode region of axon biological process from the curated GO Biological Process Annotations dataset.

forebrain regionalization Gene Set

From GO Biological Process Annotations

genes participating in the forebrain regionalization 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.

regulation of transcription regulatory region dna binding Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription regulatory region dna binding biological process from the curated GO Biological Process Annotations dataset.

maintenance of protein location in extracellular region Gene Set

From GO Biological Process Annotations

genes participating in the maintenance of protein location in extracellular region biological process from the curated GO Biological Process Annotations dataset.

protein localization to paranode region of axon Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to paranode region of axon biological process from the curated GO Biological Process Annotations dataset.

neural plate regionalization Gene Set

From GO Biological Process Annotations

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

protein localization to chromosome, telomeric region Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to chromosome, telomeric region biological process from the curated GO Biological Process Annotations dataset.

protein localization to juxtaparanode region of axon Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to juxtaparanode region of axon biological process from the curated GO Biological Process Annotations dataset.

myelin sheath adaxonal region Gene Set

From GO Cellular Component Annotations

proteins localized to the myelin sheath adaxonal region cellular component from the curated GO Cellular Component Annotations dataset.

chromosomal region Gene Set

From GO Cellular Component Annotations

proteins localized to the chromosomal region cellular component from the curated GO Cellular Component Annotations dataset.

nucleolus organizer region Gene Set

From GO Cellular Component Annotations

proteins localized to the nucleolus organizer region cellular component from the curated GO Cellular Component Annotations dataset.

condensed chromosome, centromeric region Gene Set

From GO Cellular Component Annotations

proteins localized to the condensed chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations dataset.

extracellular region part Gene Set

From GO Cellular Component Annotations

proteins localized to the extracellular region part cellular component from the curated GO Cellular Component Annotations dataset.

chromosome, centromeric region Gene Set

From GO Cellular Component Annotations

proteins localized to the chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations dataset.

internode region of axon Gene Set

From GO Cellular Component Annotations

proteins localized to the internode region of axon cellular component from the curated GO Cellular Component Annotations dataset.

extracellular region Gene Set

From GO Cellular Component Annotations

proteins localized to the extracellular region cellular component from the curated GO Cellular Component Annotations dataset.

plasma membrane region Gene Set

From GO Cellular Component Annotations

proteins localized to the plasma membrane region cellular component from the curated GO Cellular Component Annotations dataset.

host cell perinuclear region of cytoplasm Gene Set

From GO Cellular Component Annotations

proteins localized to the host cell perinuclear region of cytoplasm cellular component from the curated GO Cellular Component Annotations dataset.

membrane region Gene Set

From GO Cellular Component Annotations

proteins localized to the membrane region cellular component from the curated GO Cellular Component Annotations dataset.

myelin sheath abaxonal region Gene Set

From GO Cellular Component Annotations

proteins localized to the myelin sheath abaxonal region cellular component from the curated GO Cellular Component Annotations dataset.

juxtaparanode region of axon Gene Set

From GO Cellular Component Annotations

proteins localized to the juxtaparanode region of axon cellular component from the curated GO Cellular Component Annotations dataset.

nuclear chromosome, telomeric region Gene Set

From GO Cellular Component Annotations

proteins localized to the nuclear chromosome, telomeric region cellular component from the curated GO Cellular Component Annotations dataset.

perinuclear region of cytoplasm Gene Set

From GO Cellular Component Annotations

proteins localized to the perinuclear region of cytoplasm cellular component from the curated GO Cellular Component Annotations dataset.

paranode region of axon Gene Set

From GO Cellular Component Annotations

proteins localized to the paranode region of axon cellular component from the curated GO Cellular Component Annotations dataset.

chromosome, telomeric region Gene Set

From GO Cellular Component Annotations

proteins localized to the chromosome, telomeric region cellular component from the curated GO Cellular Component Annotations dataset.

condensed nuclear chromosome, centromeric region Gene Set

From GO Cellular Component Annotations

proteins localized to the condensed nuclear chromosome, centromeric region cellular component from the curated GO Cellular Component Annotations dataset.

rna polymerase iii regulatory region dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase iii regulatory region dna binding molecular function from the curated GO Molecular Function Annotations dataset.

proline-rich region binding Gene Set

From GO Molecular Function Annotations

genes performing the proline-rich region binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase i regulatory region dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase i regulatory region dna binding molecular function from the curated GO Molecular Function Annotations dataset.

core promoter proximal region dna binding Gene Set

From GO Molecular Function Annotations

genes performing the core promoter proximal region dna binding molecular function from the curated GO Molecular Function Annotations dataset.

transcription regulatory region sequence-specific dna binding Gene Set

From GO Molecular Function Annotations

genes performing the transcription regulatory region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii regulatory region sequence-specific dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii regulatory region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii transcription regulatory region sequence-specific dna binding transcription factor activity involved in negative regulation of transcription Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii transcription regulatory region sequence-specific dna binding transcription factor activity involved in negative regulation of transcription molecular function from the curated GO Molecular Function Annotations dataset.

intronic transcription regulatory region sequence-specific dna binding Gene Set

From GO Molecular Function Annotations

genes performing the intronic transcription regulatory region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii transcription regulatory region sequence-specific dna binding transcription factor activity involved in positive regulation of transcription Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii transcription regulatory region sequence-specific dna binding transcription factor activity involved in positive regulation of transcription molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase i regulatory region sequence-specific dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase i regulatory region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity involved in positive regulation of transcription Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity involved in positive regulation of transcription molecular function from the curated GO Molecular Function Annotations dataset.

sequence-specific transcription regulatory region dna binding rna polymerase ii transcription factor recruiting transcription factor activity Gene Set

From GO Molecular Function Annotations

genes performing the sequence-specific transcription regulatory region dna binding rna polymerase ii transcription factor recruiting transcription factor activity molecular function from the curated GO Molecular Function Annotations dataset.

regulatory region nucleic acid binding Gene Set

From GO Molecular Function Annotations

genes performing the regulatory region nucleic acid binding molecular function from the curated GO Molecular Function Annotations dataset.

mrna 3'-utr au-rich region binding Gene Set

From GO Molecular Function Annotations

genes performing the mrna 3'-utr au-rich region binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii regulatory region dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii regulatory region dna binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii core promoter proximal region sequence-specific dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii core promoter proximal region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity involved in negative regulation of transcription Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity involved in negative regulation of transcription molecular function from the curated GO Molecular Function Annotations dataset.

rna polymerase ii intronic transcription regulatory region sequence-specific dna binding Gene Set

From GO Molecular Function Annotations

genes performing the rna polymerase ii intronic transcription regulatory region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations dataset.

core promoter proximal region sequence-specific dna binding Gene Set

From GO Molecular Function Annotations

genes performing the core promoter proximal region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations dataset.

regulatory region dna binding Gene Set

From GO Molecular Function Annotations

genes performing the regulatory region dna binding molecular function from the curated GO Molecular Function Annotations dataset.

transcription regulatory region dna binding Gene Set

From GO Molecular Function Annotations

genes performing the transcription regulatory region dna binding molecular function from the curated GO Molecular Function Annotations dataset.

intronic transcription regulatory region dna binding Gene Set

From GO Molecular Function Annotations

genes performing the intronic transcription regulatory region dna binding molecular function from the curated GO Molecular Function Annotations dataset.

type 1 and type 2 muscle fiber minicore regions Gene Set

From HPO Gene-Disease Associations

genes associated with the type 1 and type 2 muscle fiber minicore regions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal shape of the frontal region Gene Set

From HPO Gene-Disease Associations

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

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.

Complex Regional Pain Syndromes Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Complex Regional Pain Syndromes phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

DNA topoisomerase, type IA, central region, subdomain 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA, central region, subdomain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA topoisomerase, type IA, central region, subdomain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA topoisomerase, type IA, central region, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal protein S4e, central region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal protein S4e, central region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Strictosidine synthase, conserved region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Strictosidine synthase, conserved region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RFX1 transcription activation region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RFX1 transcription activation region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pro-opiomelanocortin/corticotropin, ACTH, central region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pro-opiomelanocortin/corticotropin, ACTH, central region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

INO80 complex subunit B-like conserved region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the INO80 complex subunit B-like conserved region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Hermansky-Pudlak syndrome 3, central region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Hermansky-Pudlak syndrome 3, central region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TNFR/NGFR cysteine-rich region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TNFR/NGFR cysteine-rich region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

KASH5-like coiled-coil region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the KASH5-like coiled-coil region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cysteine-rich flanking region, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cysteine-rich flanking region, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transcription factor, T-box, region of unknown function Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transcription factor, T-box, region of unknown function protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ciliary BBSome complex subunit 2, middle region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ciliary BBSome complex subunit 2, middle region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

T cell CD4 receptor C-terminal region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the T cell CD4 receptor C-terminal region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sodium/calcium exchanger membrane region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sodium/calcium exchanger membrane region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tyrosine aminotransferase ubiquitination region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tyrosine aminotransferase ubiquitination region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TFIID subunit, WD40-associated region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TFIID subunit, WD40-associated region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Diffuse panbronchiolitis critical region protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Diffuse panbronchiolitis critical region protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Homogeneously-staining region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Homogeneously-staining region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Williams-Beuren syndrome chromosomal region 28 protein homologue Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Williams-Beuren syndrome chromosomal region 28 protein homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 12 protein, mammalian Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 12 protein, mammalian protein domain from the InterPro Predicted Protein Domain Annotations dataset.

SMP-30/Gluconolactonase/LRE-like region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the SMP-30/Gluconolactonase/LRE-like region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tandem-repeating region of mucin, epiglycanin-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tandem-repeating region of mucin, epiglycanin-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Rapsyn, myristoylation/linker region, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Rapsyn, myristoylation/linker region, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cat eye syndrome critical region protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cat eye syndrome critical region protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cat eye syndrome critical region protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cat eye syndrome critical region protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, alpha-2/delta subunit, conserved region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, alpha-2/delta subunit, conserved region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cat eye syndrome critical region protein 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cat eye syndrome critical region protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Elongation factor 1 beta central acidic region, eukaryote Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Elongation factor 1 beta central acidic region, eukaryote protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 12 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Amyotrophic lateral sclerosis 2 chromosomal region candidate gene 12 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Coatomer, WD associated region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Coatomer, WD associated region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Dynamin, GTPase region, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Dynamin, GTPase region, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TAFII55 protein, conserved region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TAFII55 protein, conserved region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

CMT1A duplicated region transcript 4 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CMT1A duplicated region transcript 4 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridoxal phosphate-dependent transferase, major region, subdomain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridoxal phosphate-dependent transferase, major region, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridoxal phosphate-dependent transferase, major region, subdomain 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridoxal phosphate-dependent transferase, major region, subdomain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Integrin alpha chain, C-terminal cytoplasmic region, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Integrin alpha chain, C-terminal cytoplasmic region, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mad3/BUB1 homology region 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mad3/BUB1 homology region 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cell morphogenesis central region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cell morphogenesis central region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

membrane region Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the membrane region cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

extracellular region Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the extracellular region cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

plasma membrane region Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the plasma membrane region cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

increased organ/body region tumor incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart atrium auricular region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart atrium auricular region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hippocampus ca2 region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hippocampus ca2 region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased organ/body region tumor incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hippocampus region morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hippocampus ca3 region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hippocampus ca3 region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal organ/body region tumor incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hair follicle matrix region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair follicle matrix region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hippocampus ca1 region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hippocampus ca1 region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent hippocampus ca3 region Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent hippocampus ca3 region phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal nuchal region morphology Gene Set

From MPO Gene-Phenotype Associations

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

calcified intraocular region Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the calcified intraocular region phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retrosplenial region morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal stomach cardiac region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal stomach cardiac region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

regional gastric metaplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the regional gastric metaplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal stomach pyloric region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal stomach pyloric region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hippocampus ca4 region morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hippocampus ca4 region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pretectal region morphology Gene Set

From MPO Gene-Phenotype Associations

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

Cleavage of Growing Transcript in the Termination Region Gene Set

From Reactome Pathways

proteins participating in the Cleavage of Growing Transcript in the Termination Region pathway from the Reactome Pathways dataset.

craniofacial region Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue craniofacial region from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

parahippocampal region Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

pyloric region Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

craniofacial region Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

retrosplenial region Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

extracellular region Gene Set

From LOCATE Predicted Protein Localization Annotations

proteins predicted to localize to the extracellular region cellular component from the LOCATE Predicted Protein Localization Annotations dataset.

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Hypertelorism with esophageal abnormality and hypospadias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset.

congenital nervous system abnormality Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital nervous system abnormality Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

abnormality of glucagon secretion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

gastrin secretion abnormality Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; dna damage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadasil; chromosome aberrations; chromosome abnormality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

torsion abnormality; vascular malformations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease torsion abnormality; vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; lymphocytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

smooth pursuit eye movement abnormality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormality Gene Set

From GeneRIF Biological Term Annotations

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

abnormality of vitamin metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of movement Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the endometrium Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of thyroid morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of forearm bone Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the integument Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of vitamin d metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of myeloid leukocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral subcortex Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of divalent inorganic cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

inflammatory abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the stomach Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of central motor function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vasculature Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of glycolipid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of connective tissue Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of upper limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the aortic valve Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cellular immune system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cellular immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

hearing abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of immune serum protein physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of leukocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of oral mucosa Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the urethra Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of brain morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the endocrine system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cerebral artery Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the breast Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the autonomic nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the autonomic nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pharynx Gene Set

From GWASdb SNP-Phenotype Associations

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

eeg abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the femur Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the immune system Gene Set

From GWASdb SNP-Phenotype Associations

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

morphological abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of vitamin a metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the calf Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of potassium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the carotid arteries Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of retinal arteries Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the kidney Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of circle of willis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the hand Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the pituitary gland Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the myocardium Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the biliary system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cell cycle Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of von willebrand factor Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of finger Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the lower limb Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of long bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of thrombocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of neutrophils Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the hip bone Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the upper urinary tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the iris Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the lower urinary tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiac ventricle Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of thyroid physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of hair pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

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

mesangial abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of vitamin b metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating fibrinogen Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the adrenal glands Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the intestine Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the respiratory system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of phalanx of finger Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the musculature Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral white matter Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the duodenum Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the skull base Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the astrocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the urinary system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of basophils Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of nervous system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

functional abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the face Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the male genitalia Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of facial skeleton Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the posterior segment of the eye Gene 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.

abnormality of the gingiva Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the large intestine Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the lung Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of circulating hormone level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating hormone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the placenta Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the ankles Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the femoral neck Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the heart valves Gene Set

From GWASdb SNP-Phenotype Associations

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

morphological abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of aromatic amino acid family metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of prenatal development or birth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of eye movement Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the upper limb Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral vasculature Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the ovary Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the prostate Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of amino acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of digit Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of limbs Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the testis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the anterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of dental eruption Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the clavicle Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of homocysteine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the knees Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the coronary arteries Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cardiovascular system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin adnexa Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the pleura Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the hair Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of interleukin secretion Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of blood and blood-forming tissues Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of transition element cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of tryptophan metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the head Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of head or neck Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of head or neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the mandible Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the vertebral column Gene 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.

functional respiratory abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of humoral immunity Gene Set

From GWASdb SNP-Phenotype Associations

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

neurodevelopmental abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of taste sensation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of renin-angiotensin system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of renin-angiotensin system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of pancreas physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the skeletal system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of primary teeth Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the thorax Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the thyroid gland Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the abdomen Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebrum Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebrospinal fluid Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the menstrual cycle Gene Set

From GWASdb SNP-Phenotype Associations

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

behavioral abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the oral cavity Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cholesterol metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of granulocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of monovalent inorganic cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the fundus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of forebrain morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the tongue Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of acid-base homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vertebrae Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the spinal cord Gene Set

From GWASdb SNP-Phenotype Associations

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

vascular skin abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of iron homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cornea Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of refraction Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of blood volume homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of dna repair Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the nose Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of nitrogen compound homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nitrogen compound homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of central nervous system electrophysiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of nervous system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of erythrocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of liposaccharide metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the urinary system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the vasculature of the eye Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the glomerulus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of unsaturated fatty acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiac morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of circulating protein level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating protein level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of copper homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

prenatal maternal abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the humeral diaphysis Gene Set

From GWASdb SNP-Phenotype Associations

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

phenotypic abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of reproductive system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the uterus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of female internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the curvature of the cornea Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the metaphyses Gene Set

From GWASdb SNP-Phenotype Associations

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

functional abnormality of male internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the common coagulation pathway Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of male internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hypothalamus-pituitary axis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hypothalamus-pituitary axis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of fatty-acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the genitourinary system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cytokine secretion Gene Set

From GWASdb SNP-Phenotype Associations

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

growth abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the choroid Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the globe Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of radial diaphysis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of sodium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of muscle morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the ear Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the middle ear ossicles Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cells of the monocyte/macrophage lineage Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lower limb joint Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the uvea Gene Set

From GWASdb SNP-Phenotype Associations

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

biliary tract abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the biliary tract abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the abdominal organs Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the esophagus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the retina Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the penis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of blood circulation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the radius Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of urine homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the costochondral junction Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cerebral cortex Gene Set

From GWASdb SNP-Phenotype Associations

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

venous abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of extrapyramidal motor function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of bone marrow cell morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the liver Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of proteoglycan metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of fluid regulation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of upper limb metaphysis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of metabolism/homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pylorus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of adipose tissue Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the anterior pituitary Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the nasopharynx Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the intervertebral disk Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the stapes Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the gallbladder Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the coagulation cascade Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the teeth Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the left ventricle Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of zinc homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of pelvic girdle bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

generalized abnormality of skin Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of lower limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lipid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of b cells Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the left ventricular outflow tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of carbohydrate metabolism/homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of muscle physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the glial cells Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of dental structure Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the upper arm Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the ulna Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the femoral head Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of corneal endothelium Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of lymphocytes Gene Set

From GWASdb SNP-Phenotype Associations

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

muscle abnormality related to mitochondrial dysfunction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of corneal thickness Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the mouth Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the vitamin b12 metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limb bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of magnesium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the small intestine Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the genital system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the aorta Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the female genitalia Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the humerus Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cardiovascular system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

morphological abnormality of the central nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of complement system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of cells of the erythroid lineage Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cells of the erythroid lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

chorioretinal abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of sulfur amino acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of sulfur amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating cortisol level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating cortisol level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of prothrombin Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the curvature of the vertebral column Gene 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.

abnormality of coagulation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the cervical spine Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the skull Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of carboxylic acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the pancreas Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skeletal morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the lens Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of b cell physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of body weight Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of temperature regulation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the systemic arterial tree Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the systemic arterial tree phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the rib cage Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of glycoprotein metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of vitamin e metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cell physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the eye Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the retinal vasculature Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of skin pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of ion homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the nervous system Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of macrophages Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of calcium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of male external genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of male external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of body height Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of polysaccharide metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the intrinsic pathway Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of eosinophils Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the macula Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of epidermal morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of higher mental function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of higher mental function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limb bone Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the ribs Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of nucleobase metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of the forearm Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of purine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of serum cytokine level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of serum cytokine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of immune system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of immune system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating leptin level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating leptin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the nephron Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormality of circulating glucocorticoid level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating glucocorticoid level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the level of lipoprotein cholesterol Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the level of lipoprotein cholesterol phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the neck Gene Set

From HPO Gene-Disease Associations

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

abnormality of the falx cerebri Gene Set

From HPO Gene-Disease Associations

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

abnormality of myeloid leukocytes Gene Set

From HPO Gene-Disease Associations

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

abnormality of gastrointestinal vasculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of the extraocular muscles Gene Set

From HPO Gene-Disease Associations

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

abnormality of the choanae Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycolipid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of the nasal cavity Gene Set

From HPO Gene-Disease Associations

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

abnormality of the immune system Gene Set

From HPO Gene-Disease Associations

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

abnormality of reticulocytes Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper lip Gene Set

From HPO Gene-Disease Associations

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

abnormality of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of cochlea Gene Set

From HPO Gene-Disease Associations

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

abnormality of von willebrand factor Gene Set

From HPO Gene-Disease Associations

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

abnormality of cardiac ventricle Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebellar peduncle Gene Set

From HPO Gene-Disease Associations

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

abnormality of the intestine Gene Set

From HPO Gene-Disease Associations

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

abnormality of the gingiva Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lung Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the gastrointestinal tract Gene Set

From HPO Gene-Disease Associations

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

abnormality of the basal ganglia Gene Set

From HPO Gene-Disease Associations

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

abnormality of the vena cava Gene Set

From HPO Gene-Disease Associations

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

abnormality of sharpey fibers Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thorax Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hypothalamus-pituitary axis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the head Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hairline Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cornea Gene Set

From HPO Gene-Disease Associations

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

abnormality of the frontal sinuses Gene Set

From HPO Gene-Disease Associations

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

abnormality of metacarpophalangeal joint Gene Set

From HPO Gene-Disease Associations

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

abnormality of the intrahepatic bile duct Gene Set

From HPO Gene-Disease Associations

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

abnormality of fluid regulation Gene Set

From HPO Gene-Disease Associations

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

abnormality of the philtrum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the dentate nucleus Gene Set

From HPO Gene-Disease Associations

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

abnormality of the fallopian tube Gene Set

From HPO Gene-Disease Associations

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

abnormality of secondary sexual hair Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pineal gland Gene Set

From HPO Gene-Disease Associations

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

abnormality of the crus of the helix Gene Set

From HPO Gene-Disease Associations

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

abnormality of the acetabulum Gene Set

From HPO Gene-Disease Associations

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

abnormality of vision Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sense of smell Gene Set

From HPO Gene-Disease Associations

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

abnormality of central somatosensory evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of permanent molar morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of lower limb bone Gene Set

From HPO Gene-Disease Associations

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

abnormality of muscle physiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the parathyroid physiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the corpus callosum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the achilles tendon Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thumb Gene Set

From HPO Gene-Disease Associations

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

abnormality of the myocardium Gene Set

From HPO Gene-Disease Associations

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

abnormality of complement system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the medullary cavity of the long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the phalanges of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycoprotein metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of blood glucose concentration Gene Set

From HPO Gene-Disease Associations

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

abnormality of the renal tubule Gene Set

From HPO Gene-Disease Associations

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

abnormality of the shoulder Gene Set

From HPO Gene-Disease Associations

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

abnormality of the 3rd toe Gene Set

From HPO Gene-Disease Associations

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

abnormality of forearm bone Gene Set

From HPO Gene-Disease Associations

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

abnormality of chromosome condensation Gene Set

From HPO Gene-Disease Associations

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

abnormality of prostaglandin metabolism Gene Set

From HPO Gene-Disease Associations

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

neurodevelopmental abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of connective tissue Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb bone Gene Set

From HPO Gene-Disease Associations

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

abnormality of thumb phalanx Gene Set

From HPO Gene-Disease Associations

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

abnormality of the odontoid process Gene Set

From HPO Gene-Disease Associations

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

abnormality of alanine metabolism Gene Set

From HPO Gene-Disease Associations

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

atlantoaxial abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lower limb Gene Set

From HPO Gene-Disease Associations

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

abnormality of thrombocytes Gene Set

From HPO Gene-Disease Associations

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

abnormality of the posterior pituitary Gene 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.

abnormality of the thymus Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the upper limbs Gene Set

From HPO Gene-Disease Associations

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

abnormality of the anterior chamber Gene Set

From HPO Gene-Disease Associations

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

abnormality of the vestibulocochlear nerve Gene Set

From HPO Gene-Disease Associations

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

abnormality of prenatal development or birth Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of prenatal development or birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the upper limb Gene Set

From HPO Gene-Disease Associations

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

abnormality of binocular vision Gene Set

From HPO Gene-Disease Associations

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

abnormality of the nasal septum Gene Set

From HPO Gene-Disease Associations

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

abnormality of cation homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thyroid gland Gene Set

From HPO Gene-Disease Associations

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

abnormality of the bladder Gene Set

From HPO Gene-Disease Associations

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

abnormality of the alveolar ridges Gene Set

From HPO Gene-Disease Associations

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

abnormality of forebrain morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of cerebral artery Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the choroid plexus Gene Set

From HPO Gene-Disease Associations

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

abnormality of circulating protein level Gene Set

From HPO Gene-Disease Associations

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

abnormality of pancreas morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the seventh cranial nerve Gene Set

From HPO Gene-Disease Associations

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

abnormality of the labia minora Gene Set

From HPO Gene-Disease Associations

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

abnormality of the palmar creases Gene Set

From HPO Gene-Disease Associations

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

biliary tract abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of cells of the lymphoid lineage Gene Set

From HPO Gene-Disease Associations

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

abnormality of the aortic arch Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb epiphysis morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the carpal bones Gene Set

From HPO Gene-Disease Associations

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

generalized abnormality of skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of b cells Gene Set

From HPO Gene-Disease Associations

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

abnormality of cardiac morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the glial cells Gene Set

From HPO Gene-Disease Associations

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

abnormality of the upper arm Gene Set

From HPO Gene-Disease Associations

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

abnormality of peripheral nervous system electrophysiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the aryepiglottic fold Gene Set

From HPO Gene-Disease Associations

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

abnormality of the 4th finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of cells of the erythroid lineage Gene Set

From HPO Gene-Disease Associations

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

abnormality of prothrombin Gene Set

From HPO Gene-Disease Associations

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

abnormality of the phalanges of the 4th finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of b cell physiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the nervous system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the limbs Gene Set

From HPO Gene-Disease Associations

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

abnormality of thyroid morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the scalp Gene Set

From HPO Gene-Disease Associations

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

inflammatory abnormality of the skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of the frontal hairline Gene Set

From HPO Gene-Disease Associations

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

abnormality of the retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

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

abnormality of the renal collecting system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pulmonary vasculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the femoral metaphysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of oral mucosa Gene Set

From HPO Gene-Disease Associations

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

abnormality of peripheral nerves Gene Set

From HPO Gene-Disease Associations

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

abnormality of the acoustic reflex Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the middle ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of potassium homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lip Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pituitary gland Gene Set

From HPO Gene-Disease Associations

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

tubulointerstitial abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of the dental pulp Gene Set

From HPO Gene-Disease Associations

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

abnormality of cysteine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of metabolism/homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the thenar eminence Gene Set

From HPO Gene-Disease Associations

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

abnormality of ganglioside metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of the middle phalanges of the toes Gene Set

From HPO Gene-Disease Associations

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

abnormality of humoral immunity Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sixth cranial nerve Gene Set

From HPO Gene-Disease Associations

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

abnormality of calvarial morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hip joint Gene Set

From HPO Gene-Disease Associations

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

abnormality of the humeral metaphyses Gene Set

From HPO Gene-Disease Associations

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

abnormality of urine bicarbonate concentration Gene Set

From HPO Gene-Disease Associations

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

abnormality of the genitourinary system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lymphatic vessels Gene Set

From HPO Gene-Disease Associations

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

abnormality of the fascia Gene Set

From HPO Gene-Disease Associations

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

abnormality of the ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of femoral epiphysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the radius Gene Set

From HPO Gene-Disease Associations

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

abnormality of the liver Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb metaphysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of dental color Gene Set

From HPO Gene-Disease Associations

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

abnormality of alkaline phosphatase activity Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphyses of the distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the larynx Gene Set

From HPO Gene-Disease Associations

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

chorioretinal abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of circulating hormone level Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the central nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the salivary glands Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cell physiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of primary molar morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of copper homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sacroiliac joint Gene Set

From HPO Gene-Disease Associations

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

abnormality of the diaphragm Gene Set

From HPO Gene-Disease Associations

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

abnormality of movement Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lacrimal duct Gene Set

From HPO Gene-Disease Associations

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

abnormality of the proximal tibial epiphysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the aortic valve Gene Set

From HPO Gene-Disease Associations

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

abnormality of the corticospinal tract Gene Set

From HPO Gene-Disease Associations

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

abnormality of the endocrine system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the tarsal bones Gene Set

From HPO Gene-Disease Associations

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

abnormality of the soft palate Gene Set

From HPO Gene-Disease Associations

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

abnormality of the adrenal glands Gene Set

From HPO Gene-Disease Associations

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

abnormality of the respiratory system Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of fontanelles Gene Set

From HPO Gene-Disease Associations

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

abnormality of the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

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

abnormality of the septum pellucidum Gene Set

From HPO Gene-Disease Associations

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

abnormality of renal excretion Gene Set

From HPO Gene-Disease Associations

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

abnormality of the premaxilla Gene Set

From HPO Gene-Disease Associations

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

eeg abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of renin-angiotensin system Gene Set

From HPO Gene-Disease Associations

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

abnormality of pancreas physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of pancreas physiology 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.

abnormality of the skin Gene Set

From HPO Gene-Disease Associations

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

abnormality of lower lip Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pectoral muscle Gene Set

From HPO Gene-Disease Associations

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

abnormality of descemet's membrane Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of descemet's membrane phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the sclera Gene Set

From HPO Gene-Disease Associations

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

phenotypic abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of circulating adrenocorticotropin level Gene Set

From HPO Gene-Disease Associations

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

abnormality of the radial head Gene Set

From HPO Gene-Disease Associations

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

abnormality of saccadic eye movements Gene Set

From HPO Gene-Disease Associations

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

abnormality of somatosensory evoked potentials Gene Set

From HPO Gene-Disease Associations

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

abnormality of the uvea Gene Set

From HPO Gene-Disease Associations

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

abnormality of female external genitalia Gene Set

From HPO Gene-Disease Associations

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

abnormality of tyrosine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of extrapyramidal motor function Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the thorax Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cardiovascular system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the proximal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of the rectum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphysis of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of carbohydrate metabolism/homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the ulna Gene Set

From HPO Gene-Disease Associations

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

abnormality of the supraorbital ridges Gene Set

From HPO Gene-Disease Associations

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

abnormality of the coagulation cascade Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycosaminoglycan metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of the extrinsic pathway Gene Set

From HPO Gene-Disease Associations

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

abnormality of skeletal morphology Gene Set

From HPO Gene-Disease Associations

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

morphological abnormality of the vestibule of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skin adnexa Gene Set

From HPO Gene-Disease Associations

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

abnormality of limb bone Gene Set

From HPO Gene-Disease Associations

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

abnormality of the mitral valve Gene Set

From HPO Gene-Disease Associations

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

abnormality of orotic acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of neutrophil physiology Gene Set

From HPO Gene-Disease Associations

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

abnormality of glycine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of globe location Gene Set

From HPO Gene-Disease Associations

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

abnormality of the scapula Gene Set

From HPO Gene-Disease Associations

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

abnormality of t cells Gene Set

From HPO Gene-Disease Associations

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

abnormality of dicarboxylic acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of cells of the granulocytic lineage Gene Set

From HPO Gene-Disease Associations

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

abnormality of the femur Gene Set

From HPO Gene-Disease Associations

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

abnormality of upper limb joint Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pancreatic islet cells Gene Set

From HPO Gene-Disease Associations

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

abnormality of long bone morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of the lymphatic system Gene Set

From HPO Gene-Disease Associations

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

mesangial abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphyses of the 3rd finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of the patella Gene Set

From HPO Gene-Disease Associations

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

blood group antigen abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the blood group antigen abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of glycolysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the optic disc Gene Set

From HPO Gene-Disease Associations

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

abnormality of dermal melanosomes Gene Set

From HPO Gene-Disease Associations

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

abnormality of leucine metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of b cell number Gene Set

From HPO Gene-Disease Associations

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

abnormality of the renal cortex Gene Set

From HPO Gene-Disease Associations

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

abnormality of the ventricular septum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the pelvis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the fetal cardiovascular system Gene Set

From HPO Gene-Disease Associations

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

abnormality of nitrogen compound homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the 3rd metacarpal Gene Set

From HPO Gene-Disease Associations

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

abnormality of the palate Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the palate 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.

abnormality of the mandible Gene Set

From HPO Gene-Disease Associations

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

abnormality of the sinuses Gene Set

From HPO Gene-Disease Associations

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

abnormality of the pubic hair Gene Set

From HPO Gene-Disease Associations

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

abnormality of proteoglycan metabolism Gene Set

From HPO Gene-Disease Associations

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

muscle abnormality related to mitochondrial dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the macula Gene Set

From HPO Gene-Disease Associations

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

abnormality of the styloid process of ulna Gene Set

From HPO Gene-Disease Associations

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

abnormality of skull ossification Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the upper arm Gene Set

From HPO Gene-Disease Associations

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

abnormality of vision evoked potentials Gene Set

From HPO Gene-Disease Associations

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

abnormality of the labia majora Gene Set

From HPO Gene-Disease Associations

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

abnormality of the genital system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the humerus Gene Set

From HPO Gene-Disease Associations

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

abnormality of lens shape Gene Set

From HPO Gene-Disease Associations

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

abnormality of the eye Gene Set

From HPO Gene-Disease Associations

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

abnormality of the uvula Gene Set

From HPO Gene-Disease Associations

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

abnormality of lateral ventricle Gene Set

From HPO Gene-Disease Associations

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

abnormality of chromosome segregation Gene Set

From HPO Gene-Disease Associations

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

abnormality of higher mental function Gene Set

From HPO Gene-Disease Associations

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

inflammatory abnormality of the eye Gene Set

From HPO Gene-Disease Associations

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

abnormality of vitamin k metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of the nasal bone Gene Set

From HPO Gene-Disease Associations

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

abnormality of the conjunctiva Gene Set

From HPO Gene-Disease Associations

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

abnormality of amino acid metabolism Gene Set

From HPO Gene-Disease Associations

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

abnormality of the chin Gene Set

From HPO Gene-Disease Associations

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

abnormality of cardiac atrium Gene Set

From HPO Gene-Disease Associations

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

abnormality of pain sensation Gene Set

From HPO Gene-Disease Associations

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

abnormality of the distal femoral epiphysis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the menstrual cycle Gene Set

From HPO Gene-Disease Associations

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

abnormality of the anterior fontanelle Gene Set

From HPO Gene-Disease Associations

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

abnormality of the plantar skin of foot Gene Set

From HPO Gene-Disease Associations

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

abnormality of pyruvate family amino acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of pyruvate family amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sacrococcygeal pilonidal abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of adrenal morphology Gene Set

From HPO Gene-Disease Associations

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

abnormality of carpal bone ossification Gene Set

From HPO Gene-Disease Associations

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

abnormality of male internal genitalia Gene Set

From HPO Gene-Disease Associations

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

abnormality of the eyelashes Gene Set

From HPO Gene-Disease Associations

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

abnormality of the cerebral vasculature Gene Set

From HPO Gene-Disease Associations

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

abnormality of urine hormone level Gene Set

From HPO Gene-Disease Associations

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

abnormality of mast cells Gene Set

From HPO Gene-Disease Associations

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

abnormality of globe size Gene Set

From HPO Gene-Disease Associations

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

abnormality of the eyebrow Gene Set

From HPO Gene-Disease Associations

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

vascular skin abnormality Gene Set

From HPO Gene-Disease Associations

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

abnormality of central nervous system electrophysiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of central nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the foramen magnum Gene Set

From HPO Gene-Disease Associations

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

abnormality of the phalanges of the 3rd finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

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

abnormality of hand joint mobility Gene Set

From HPO Gene-Disease Associations

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

abnormality of the urinary system Gene Set

From HPO Gene-Disease Associations

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

abnormality of the dorsal column of the spinal cord Gene Set

From HPO Gene-Disease Associations

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

abnormality of the costochondral junction Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiglottis Gene Set

From HPO Gene-Disease Associations

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

abnormality of hair growth rate Gene Set

From HPO Gene-Disease Associations

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

abnormality of fatty-acid anion metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of fatty-acid anion metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphysis of the 1st metacarpal Gene Set

From HPO Gene-Disease Associations

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

abnormality of magnesium homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormality of the ureter Gene Set

From HPO Gene-Disease Associations

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

abnormality of color vision Gene Set

From HPO Gene-Disease Associations

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