| Name |
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AOC2 Geneamine oxidase, copper containing 2 (retina-specific) Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes and ammonia in the presence of copper and quinone cofactor. This gene shows high sequence similarity to copper amine oxidases from various species ranging from bacteria to mammals. The protein contains several conserved motifs including the active site of amine oxidases and the histidine residues that likely bind copper. It may be a critical modulator of signal transmission in retina, possibly by degrading the biogenic amines dopamine, histamine, and putrescine. This gene may be a candidate gene for hereditary ocular diseases. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008] |
SLC31A1 Genesolute carrier family 31 (copper transporter), member 1 The protein encoded by this gene is a high-affinity copper transporter found in the cell membrane. The encoded protein functions as a homotrimer to effect the uptake of dietary copper. [provided by RefSeq, Aug 2011] |
SLC31A2 Genesolute carrier family 31 (copper transporter), member 2 Enables copper ion transmembrane transporter activity. Involved in copper ion import. Located in late endosome membrane; lysosomal membrane; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SLC31A1P1 Genesolute carrier family 31 (copper transporter), member 1 pseudogene 1 |
COX17P1 GeneCOX17 cytochrome c oxidase copper chaperone pseudogene 1 |
AOC3 Geneamine oxidase, copper containing 3 This gene encodes a member of the semicarbazide-sensitive amine oxidase family. Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes in the presence of copper and quinone cofactor. The encoded protein is localized to the cell surface, has adhesive properties as well as monoamine oxidase activity, and may be involved in leukocyte trafficking. Alterations in levels of the encoded protein may be associated with many diseases, including diabetes mellitus. A pseudogene of this gene has been described and is located approximately 9-kb downstream on the same chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013] |
AOC4P Geneamine oxidase, copper containing 4, pseudogene |
AOC1 Geneamine oxidase, copper containing 1 This gene encodes a metal-binding membrane glycoprotein that oxidatively deaminates putrescine, histamine, and related compounds. The encoded protein is inhibited by amiloride, a diuretic that acts by closing epithelial sodium ion channels. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2013] |
ATOX1 Geneantioxidant 1 copper chaperone This gene encodes a copper chaperone that plays a role in copper homeostasis by binding and transporting cytosolic copper to ATPase proteins in the trans-Golgi network for later incorporation to the ceruloplasmin. This protein also functions as an antioxidant against superoxide and hydrogen peroxide, and therefore, may play a significant role in cancer carcinogenesis. Because of its cytogenetic location, this gene represents a candidate gene for 5q-syndrome. [provided by RefSeq, Jul 2008] |
COX11 GeneCOX11 cytochrome c oxidase copper chaperone Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be a heme A biosynthetic enzyme involved in COX formation, according to the yeast mutant studies. However, the studies in Rhodobacter sphaeroides suggest that this gene is not required for heme A biosynthesis, but required for stable formation of the Cu(B) and magnesium centers of COX. This human protein is predicted to contain a transmembrane domain localized in the mitochondrial inner membrane. Multiple transcript variants encoding different isoforms have been found for this gene. A related pseudogene has been found on chromosome 6. [provided by RefSeq, Jun 2009] |
COX17 GeneCOX17 cytochrome c oxidase copper chaperone Cytochrome c oxidase (COX), the terminal component of the mitochondrial respiratory chain, catalyzes the electron transfer from reduced cytochrome c to oxygen. This component is a heteromeric complex consisting of 3 catalytic subunits encoded by mitochondrial genes and multiple structural subunits encoded by nuclear genes. The mitochondrially-encoded subunits function in electron transfer, and the nuclear-encoded subunits may function in the regulation and assembly of the complex. This nuclear gene encodes a protein which is not a structural subunit, but may be involved in the recruitment of copper to mitochondria for incorporation into the COX apoenzyme. This protein shares 92% amino acid sequence identity with mouse and rat Cox17 proteins. This gene is no longer considered to be a candidate gene for COX deficiency. A pseudogene COX17P has been found on chromosome 13. [provided by RefSeq, Jul 2008] |
CUTC GenecutC copper transporter Members of the CUT family of copper transporters are associated with copper homeostasis and are involved in the uptake, storage, delivery, and efflux of copper (Gupta et al., 1995 [PubMed 7635807]; Li et al., 2005 [PubMed 16182249]).[supplied by OMIM, Mar 2008] |
COX11P1 GeneCOX11 cytochrome c oxidase copper chaperone pseudogene 1 |
CCS Genecopper chaperone for superoxide dismutase Copper chaperone for superoxide dismutase specifically delivers Cu to copper/zinc superoxide dismutase and may activate copper/zinc superoxide dismutase through direct insertion of the Cu cofactor. [provided by RefSeq, Jul 2008] |
COMMD1 Genecopper metabolism (Murr1) domain containing 1 Enables several functions, including phosphatidylinositol-3,4-bisphosphate binding activity; phospholipid binding activity; and protein homodimerization activity. Involved in several processes, including Golgi to plasma membrane transport; negative regulation of protein localization to cell surface; and regulation of protein metabolic process. Acts upstream of or within negative regulation of NF-kappaB transcription factor activity. Located in cytosol; endosome; and nucleoplasm. Part of Cul2-RING ubiquitin ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
abnormality of copper homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of copper homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of copper homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of Copper Homeostasis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Copper Homeostasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
cellular copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular copper ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
Copper homeostasis protein CutC Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper homeostasis protein CutC protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper homeostasis CutC domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper homeostasis CutC domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal copper homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal copper homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
intracellular copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular copper ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the copper ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal copper homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal copper homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Copper homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Copper homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
intracellular copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular copper ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
copper ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the copper ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
abnormality of divalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of potassium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of transition element cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of monovalent inorganic cation homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of acid-base homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of iron homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of iron homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood volume homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nitrogen compound homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nitrogen compound homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sodium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sodium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of urine homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of urine homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of zinc homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of zinc homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carbohydrate metabolism/homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of magnesium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of magnesium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of ion homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of ion homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of calcium homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of calcium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cation homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of potassium homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of potassium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metabolism/homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of carbohydrate metabolism/homeostasis Gene SetFrom 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 nitrogen compound homeostasis Gene SetFrom 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 magnesium homeostasis Gene SetFrom 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 urine homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of urine homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of iron homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of iron homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of phosphate homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of phosphate homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of transition element cation homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of transition element cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of divalent inorganic cation homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of divalent inorganic cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of ion homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of ion homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of sodium homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of sodium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of chloride homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of chloride homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of calcium homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of calcium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of acid-base homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of acid-base homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of monovalent inorganic cation homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of zinc homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of zinc homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormality Of Metabolism/Homeostasis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Metabolism/Homeostasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Iron Homeostasis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Iron Homeostasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Carbohydrate Metabolism/Homeostasis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Carbohydrate Metabolism/Homeostasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Urine Homeostasis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Urine Homeostasis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality of metabolism/homeostasis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormality of metabolism/homeostasis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
copper sulfate-500 Gene SetFrom CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-500 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset. |
copper sulfate-438 Gene SetFrom CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-438 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset. |
copper sulfate-459 Gene SetFrom CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-459 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset. |
copper sulfate-575 Gene SetFrom CMAP Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the copper sulfate-575 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset. |
copper bis(3,5-diisopropylsalicylate) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper bis(3,5-diisopropylsalicylate) from the curated CTD Gene-Chemical Interactions dataset. |
copper protoporphyrin IX Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper protoporphyrin IX from the curated CTD Gene-Chemical Interactions dataset. |
Copper Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Copper from the curated CTD Gene-Chemical Interactions dataset. |
bis((2-oxindol-3-ylimino)-2-(2-aminoethyl)pyridine-N,N')copper(II) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical bis((2-oxindol-3-ylimino)-2-(2-aminoethyl)pyridine-N,N')copper(II) from the curated CTD Gene-Chemical Interactions dataset. |
copper pyruvaldehyde bis(N(4)-methylthiosemicarbazone) complex Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper pyruvaldehyde bis(N(4)-methylthiosemicarbazone) complex from the curated CTD Gene-Chemical Interactions dataset. |
(4,4-dimethyl-2,2-bipyridine)(acetylacetonate)copper(II) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical (4,4-dimethyl-2,2-bipyridine)(acetylacetonate)copper(II) from the curated CTD Gene-Chemical Interactions dataset. |
(4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical (4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II) from the curated CTD Gene-Chemical Interactions dataset. |
Copper Sulfate Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Copper Sulfate from the curated CTD Gene-Chemical Interactions dataset. |
copper (N-2-hydroxyacetophenone)glycinate Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper (N-2-hydroxyacetophenone)glycinate from the curated CTD Gene-Chemical Interactions dataset. |
copper histidine Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper histidine from the curated CTD Gene-Chemical Interactions dataset. |
copper (II) diacetyl-di(N(4)-methylthiosemicarbazone) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical copper (II) diacetyl-di(N(4)-methylthiosemicarbazone) from the curated CTD Gene-Chemical Interactions dataset. |
copper Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term copper in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
regulation of copper ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion import biological process from the curated GO Biological Process Annotations 2015 dataset. |
detoxification of copper ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the detoxification of copper ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion export Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion export biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to copper ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to copper ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion import into cell Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion import into cell biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to copper ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to copper ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to copper ion starvation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to copper ion starvation biological process from the curated GO Biological Process Annotations 2015 dataset. |
intracellular copper ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intracellular copper ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
plasma membrane copper ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the plasma membrane copper ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
copper ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper ion binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper ion binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper uptake transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper uptake transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
heme-copper terminal oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the heme-copper terminal oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper chaperone activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper-transporting atpase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper-transporting atpase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper-dependent protein binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper-dependent protein binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
superoxide dismutase copper chaperone activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the superoxide dismutase copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
copper-exporting atpase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the copper-exporting atpase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Copper Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Copper metabolite from the curated HMDB Metabolites of Enzymes dataset. |
high nonceruloplasmin-bound serum copper Gene SetFrom HPO Gene-Disease Associations genes associated with the high nonceruloplasmin-bound serum copper phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Copper amine oxidase, N2/N3-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N2/N3-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome c oxidase copper chaperone Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase copper chaperone protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper centre Cu(A) Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper centre Cu(A) protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-2 conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-2 conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aromatic amino acid hydroxylase, iron/copper binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aromatic amino acid hydroxylase, iron/copper binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised domain, di-copper centre Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised domain, di-copper centre protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper chaperone SCO1/SenC Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper chaperone SCO1/SenC protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper type II, ascorbate-dependent monooxygenase-like, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper amine oxidase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-1 conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase, histidine-cluster-1 conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tyrosinase copper-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tyrosinase copper-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ctr copper transporter Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ctr copper transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Superoxide dismutase, copper/zinc, binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Superoxide dismutase, copper/zinc, binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Superoxide dismutase, copper/zinc binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Superoxide dismutase, copper/zinc binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Heavy metal-associated domain, copper ion-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Heavy metal-associated domain, copper ion-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Amyloidogenic glycoprotein, copper-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Amyloidogenic glycoprotein, copper-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper amine oxidase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Periplasmic copper-binding protein NosD, beta helix domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Periplasmic copper-binding protein NosD, beta helix domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper amine oxidase, N2-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N2-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper type II, ascorbate-dependent monooxygenase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper type II, ascorbate-dependent monooxygenase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper amine oxidase, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Copper amine oxidase, N3-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Copper amine oxidase, N3-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Multicopper oxidase, copper-binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Multicopper oxidase, copper-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Multi-copper polyphenol oxidoreductase, laccase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Multi-copper polyphenol oxidoreductase, laccase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome c oxidase, subunit I, copper-binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit I, copper-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
decreased circulating copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal liver copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased liver copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased intestine copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased intestine copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestine copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestine copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased liver copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased brain copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brain copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased kidney copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased kidney copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased circulating copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brain copper level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brain copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Copper-Overload Cirrhosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Copper-Overload Cirrhosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Copper Toxicosis, Idiopathic Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Copper Toxicosis, Idiopathic in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
High Nonceruloplasmin-Bound Serum Copper Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype High Nonceruloplasmin-Bound Serum Copper in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Copper Accumulation In Liver Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Copper Accumulation In Liver in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Urinary Copper Concentration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Urinary Copper Concentration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
copper ion transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the copper ion transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein maturation by copper ion transfer Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein maturation by copper ion transfer biological process from the curated GO Biological Process Annotations 2023 dataset. |
copper ion import Gene SetFrom GO Biological Process Annotations 2023 genes participating in the copper ion import biological process from the curated GO Biological Process Annotations 2023 dataset. |
plasma membrane copper ion transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the plasma membrane copper ion transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to copper ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to copper ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to copper ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to copper ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to copper ion starvation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to copper ion starvation biological process from the curated GO Biological Process Annotations 2023 dataset. |
copper ion export Gene SetFrom GO Biological Process Annotations 2023 genes participating in the copper ion export biological process from the curated GO Biological Process Annotations 2023 dataset. |
copper ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to copper ion starvation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to copper ion starvation biological process from the curated GO Biological Process Annotations 2023 dataset. |
copper ion binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the copper ion binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
copper ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the copper ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
P-type divalent copper transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the P-type divalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
superoxide dismutase copper chaperone activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the superoxide dismutase copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
P-type monovalent copper transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the P-type monovalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
decreased brain copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased liver copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased liver copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal liver copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brain copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brain copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased liver copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased liver copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased circulating copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased circulating copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased kidney copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased kidney copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased intestine copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased intestine copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brainstem copper level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brainstem copper level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Copper metabolism Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Copper metabolism pathway from the WikiPathways Pathways 2024 dataset. |
copper ion transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the copper ion transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
copper ion import Gene SetFrom GO Biological Process Annotations 2025 genes participating in the copper ion import biological process from the curated GO Biological Process Annotations 2025 dataset. |
plasma membrane copper ion transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the plasma membrane copper ion transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to copper ion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to copper ion biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to copper ion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to copper ion biological process from the curated GO Biological Process Annotations 2025 dataset. |
copper ion export Gene SetFrom GO Biological Process Annotations 2025 genes participating in the copper ion export biological process from the curated GO Biological Process Annotations 2025 dataset. |
copper ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the copper ion transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
copper ion binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the copper ion binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
copper ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the copper ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
P-type divalent copper transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the P-type divalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
superoxide dismutase copper chaperone activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the superoxide dismutase copper chaperone activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
P-type monovalent copper transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the P-type monovalent copper transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Copper deficiency myelopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Copper deficiency myelopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Copper ion transmembrane transporter complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Copper ion transmembrane transporter complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Superoxide dismutase copper chaperone complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Superoxide dismutase copper chaperone complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Copper levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Copper levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
COPPER CHLORIDE Gene Setinteracting proteins for the COPPER CHLORIDE drug from theDGIdb Drug Targets 2026 dataset. |
apoptotic dna-fragmentation and tissue homeostasis Gene SetFrom Biocarta Pathways proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset. |
calcium homeostasis and peripheral bone density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease calcium homeostasis and peripheral bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
type 2 diabetes related glucose homeostasis trait Gene SetFrom GAD Gene-Disease Associations genes associated with the disease type 2 diabetes related glucose homeostasis trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
type 2 diabetes related glucose homeostasis traits Gene SetFrom GAD Gene-Disease Associations genes associated with the disease type 2 diabetes related glucose homeostasis traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
more degree of homeostasis model assessment ir Gene SetFrom GAD Gene-Disease Associations genes associated with the disease more degree of homeostasis model assessment ir in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity and glucose homeostasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity and glucose homeostasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose homeostasis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose homeostasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
homeostasis Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term homeostasis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
sodium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the sodium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular trivalent inorganic anion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular trivalent inorganic anion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
urate homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the urate homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
energy homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the energy homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
metal ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metal ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
chemical homeostasis within a tissue Gene SetFrom GO Biological Process Annotations 2015 genes participating in the chemical homeostasis within a tissue biological process from the curated GO Biological Process Annotations 2015 dataset. |
nitric oxide homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nitric oxide homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
renal water homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the renal water homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
water homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the water homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
acylglycerol homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the acylglycerol homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
transition metal ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the transition metal ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular chemical homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular chemical homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular metal ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular metal ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
divalent inorganic anion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the divalent inorganic anion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
b-1 b cell homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the b-1 b cell homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular triglyceride homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular triglyceride homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
muscle cell cellular homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the muscle cell cellular homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cell volume homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cell volume homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular divalent inorganic anion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular divalent inorganic anion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular monovalent inorganic anion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular monovalent inorganic anion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular water homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular water homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
temperature homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the temperature homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
myeloid cell homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the myeloid cell homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular potassium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular potassium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of energy homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of energy homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular magnesium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular magnesium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
urea homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the urea homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular iron ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular monovalent inorganic cation homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular monovalent inorganic cation homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
amino acid homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the amino acid homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
monovalent inorganic cation homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the monovalent inorganic cation homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
phosphate ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phosphate ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
multicellular organismal water homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the multicellular organismal water homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
magnesium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the magnesium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
epidermal stem cell homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the epidermal stem cell homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cell redox homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cell redox homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular zinc ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular zinc ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cation homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cation homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the iron ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
gas homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the gas homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
endoplasmic reticulum calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the endoplasmic reticulum calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular ammonia homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular ammonia homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
anatomical structure homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the anatomical structure homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
mitochondrial calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the mitochondrial calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
t cell homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the t cell homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
tissue homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the tissue homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cell proliferation involved in tissue homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cell proliferation involved in tissue homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
homeostasis of number of cells Gene SetFrom GO Biological Process Annotations 2015 genes participating in the homeostasis of number of cells biological process from the curated GO Biological Process Annotations 2015 dataset. |
carbohydrate homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the carbohydrate homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
smooth endoplasmic reticulum calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the smooth endoplasmic reticulum calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cadmium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cadmium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular chloride ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular chloride ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
creatinine homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the creatinine homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of energy homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of energy homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
phospholipid homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phospholipid homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular transition metal ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular transition metal ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
anion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the anion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
hematopoietic stem cell homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hematopoietic stem cell homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
trivalent inorganic anion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the trivalent inorganic anion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
b cell homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the b cell homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
potassium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the potassium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
ammonia homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ammonia homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
sterol homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the sterol homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular anion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular anion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of cholesterol homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of cholesterol homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
ubiquitin homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ubiquitin homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
oxygen homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the oxygen homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of cholesterol homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of cholesterol homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular urea homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular urea homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular cation homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular cation homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cholesterol homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cholesterol homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular sodium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular sodium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
homeostasis of number of cells in a free-living population Gene SetFrom GO Biological Process Annotations 2015 genes participating in the homeostasis of number of cells in a free-living population biological process from the curated GO Biological Process Annotations 2015 dataset. |
calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular creatinine homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular creatinine homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
circadian temperature homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the circadian temperature homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular sphingolipid homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular sphingolipid homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
retina homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the retina homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
fatty acid homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fatty acid homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
leukocyte homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the leukocyte homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular glucose homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular glucose homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
chloride ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the chloride ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
homeostasis of number of cells within a tissue Gene SetFrom GO Biological Process Annotations 2015 genes participating in the homeostasis of number of cells within a tissue biological process from the curated GO Biological Process Annotations 2015 dataset. |
divalent inorganic cation homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the divalent inorganic cation homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cytosolic calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cytosolic calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
erythrocyte homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the erythrocyte homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular phosphate ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular phosphate ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
multicellular organismal iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the multicellular organismal iron ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
neuron cellular homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the neuron cellular homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
polyamine homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the polyamine homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
multicellular organismal homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the multicellular organismal homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of energy homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of energy homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cartilage homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cartilage homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
zinc ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the zinc ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
lymphocyte homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lymphocyte homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
triglyceride homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the triglyceride homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular cadmium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular cadmium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
neutrophil homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the neutrophil homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
golgi calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the golgi calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular divalent inorganic cation homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular divalent inorganic cation homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
monovalent inorganic anion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the monovalent inorganic anion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
inorganic ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inorganic ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
surfactant homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the surfactant homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
chemical homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the chemical homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of gluconeogenesis involved in cellular glucose homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of gluconeogenesis involved in cellular glucose homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
glucose homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the glucose homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
Homeostasis model assessment of beta-cell function (interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Homeostasis model assessment of beta-cell function (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Homeostasis model assessment of insulin resistance (interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Homeostasis model assessment of insulin resistance (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormal glucose homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glucose homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sweat homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sweat homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cholesterol homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cholesterol homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Calcium homeostasis modulator protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Calcium homeostasis modulator protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Calcium homeostasis modulator protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Calcium homeostasis modulator protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Calcium homeostasis modulator protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Calcium homeostasis modulator protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal gas homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gas homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glycogen homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glycogen homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear endolymph ionic homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear endolymph ionic homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal galactose homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal galactose homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bile salt homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bile salt homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ion homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ion homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
homeostasis/metabolism phenotype Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the homeostasis/metabolism phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal magnesium ion homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal magnesium ion homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glucose homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glucose homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal calcium ion homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal calcium ion homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mineral homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mineral homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sodium ion homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sodium ion homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nitric oxide homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nitric oxide homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal potassium ion homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal potassium ion homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circadian temperature homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circadian temperature homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cholesterol homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cholesterol homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular endolymph ionic homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular endolymph ionic homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal energy homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal energy homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blood homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blood homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal iron homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal iron homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal body temperature homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body temperature homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal water homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal water homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zinc homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zinc homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lipid homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lipid homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vitamin homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vitamin homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
homeostasis Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term homeostasis in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Hypoxic and oxygen homeostasis regulation of HIF-1-alpha Gene SetFrom PID Pathways proteins participating in the Hypoxic and oxygen homeostasis regulation of HIF-1-alpha pathway from the PID Pathways dataset. |
Cell redox homeostasis Gene Setproteins participating in the Cell redox homeostasis pathway from the Reactome Pathways dataset. |
Platelet homeostasis Gene Setproteins participating in the Platelet homeostasis pathway from the Reactome Pathways dataset. |
Platelet calcium homeostasis Gene Setproteins participating in the Platelet calcium homeostasis pathway from the Reactome Pathways dataset. |
ABCA transporters in lipid homeostasis Gene Setproteins participating in the ABCA transporters in lipid homeostasis pathway from the Reactome Pathways dataset. |
Vasopressin regulates renal water homeostasis via Aquaporins Gene Setproteins participating in the Vasopressin regulates renal water homeostasis via Aquaporins pathway from the Reactome Pathways dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
Iron Homeostasis(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Iron Homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
endoplasmic reticulum calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the endoplasmic reticulum calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
retina homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the retina homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
phospholipid homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phospholipid homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular glucose homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular glucose homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
T cell homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the T cell homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
cholesterol homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cholesterol homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
glucose homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the glucose homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
hematopoietic stem cell homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the hematopoietic stem cell homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intestinal stem cell homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intestinal stem cell homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
renal water homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the renal water homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
chloride ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the chloride ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular iron ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular phosphate ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular phosphate ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular glutamate homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular glutamate homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
mitochondrial calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mitochondrial calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
phosphate ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the phosphate ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
surfactant homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the surfactant homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
ammonium homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the ammonium homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
maintenance of blood vessel diameter homeostasis by renin-angiotensin Gene SetFrom GO Biological Process Annotations 2023 genes participating in the maintenance of blood vessel diameter homeostasis by renin-angiotensin biological process from the curated GO Biological Process Annotations 2023 dataset. |
fatty acid homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the fatty acid homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
triglyceride homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the triglyceride homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular monoatomic ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular monoatomic ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular oxygen homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular oxygen homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular sodium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular sodium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular potassium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular potassium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular zinc ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular zinc ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
B cell homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the B cell homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
multicellular organismal-level iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the multicellular organismal-level iron ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular water homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular water homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
multicellular organismal-level water homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the multicellular organismal-level water homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular triglyceride homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular triglyceride homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
sterol homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the sterol homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
potassium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the potassium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
sodium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the sodium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
B-1 B cell homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the B-1 B cell homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
homeostasis of number of cells within a tissue Gene SetFrom GO Biological Process Annotations 2023 genes participating in the homeostasis of number of cells within a tissue biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular monoatomic cation homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular monoatomic cation homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular amino acid homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular amino acid homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of cell proliferation involved in tissue homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of cell proliferation involved in tissue homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
cartilage homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cartilage homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular chloride ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular chloride ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
Golgi calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the Golgi calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular nitric oxide homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular nitric oxide homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
magnesium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the magnesium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
manganese ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the manganese ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
acylglycerol homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the acylglycerol homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular manganese ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular manganese ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular magnesium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular magnesium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular sphingolipid homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular sphingolipid homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
monoatomic cation homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the monoatomic cation homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
smooth endoplasmic reticulum calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the smooth endoplasmic reticulum calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
monoatomic anion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the monoatomic anion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular monoatomic anion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular monoatomic anion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal urine homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal urine homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cholesterol homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cholesterol homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lipid homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lipid homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal iron homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal iron homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal blood homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal blood homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal glucose homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal glucose homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bile salt homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bile salt homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal glycogen homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal glycogen homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ion homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ion homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal nitric oxide homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal nitric oxide homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal calcium ion homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal calcium ion homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal energy homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal energy homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal gas homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal gas homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal body temperature homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal body temperature homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circadian temperature homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circadian temperature homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal zinc homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal zinc homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear endolymph ionic homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear endolymph ionic homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal mineral homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal mineral homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal potassium ion homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal potassium ion homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal galactose homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal galactose homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sodium ion homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sodium ion homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular endolymph ionic homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular endolymph ionic homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ammonia homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ammonia homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vitamin homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vitamin homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal magnesium ion homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal magnesium ion homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal renal water homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal renal water homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
homeostasis/metabolism phenotype Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the homeostasis/metabolism phenotype phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal bicarbonate homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bicarbonate homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cholesterol homeostasis Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal cholesterol homeostasis phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Zinc homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Zinc homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
GLP 1 from intestine and pancreas and role in glucose homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the GLP 1 from intestine and pancreas and role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Glucose homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
ABC transporters in lipid homeostasis Gene Setproteins participating in the ABC transporters in lipid homeostasis pathway from the Reactome Pathways 2024 dataset. |
Ion homeostasis Gene Setproteins participating in the Ion homeostasis pathway from the Reactome Pathways 2024 dataset. |
NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis Gene Setproteins participating in the NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis pathway from the Reactome Pathways 2024 dataset. |
Platelet calcium homeostasis Gene Setproteins participating in the Platelet calcium homeostasis pathway from the Reactome Pathways 2024 dataset. |
Platelet homeostasis Gene Setproteins participating in the Platelet homeostasis pathway from the Reactome Pathways 2024 dataset. |
Vasopressin regulates renal water homeostasis via Aquaporins Gene Setproteins participating in the Vasopressin regulates renal water homeostasis via Aquaporins pathway from the Reactome Pathways 2024 dataset. |
endoplasmic reticulum calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the endoplasmic reticulum calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
retina homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the retina homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
phospholipid homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phospholipid homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular glucose homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular glucose homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
fatty acid homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the fatty acid homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
T cell homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the T cell homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
cholesterol homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cholesterol homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular iron ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
glucose homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the glucose homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
hematopoietic stem cell homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the hematopoietic stem cell homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intestinal stem cell homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intestinal stem cell homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
renal water homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the renal water homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
chloride ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the chloride ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular phosphate ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular phosphate ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular glutamate homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular glutamate homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
mitochondrial calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mitochondrial calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
phosphate ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the phosphate ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
surfactant homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the surfactant homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
ammonium homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the ammonium homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
maintenance of blood vessel diameter homeostasis by renin-angiotensin Gene SetFrom GO Biological Process Annotations 2025 genes participating in the maintenance of blood vessel diameter homeostasis by renin-angiotensin biological process from the curated GO Biological Process Annotations 2025 dataset. |
triglyceride homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the triglyceride homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular monoatomic ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular monoatomic ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
multicellular organismal-level iron ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the multicellular organismal-level iron ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular oxygen homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular oxygen homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular sodium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular sodium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular potassium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular potassium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular zinc ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular zinc ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
B cell homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the B cell homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular water homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular water homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
multicellular organismal-level water homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the multicellular organismal-level water homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular ammonium homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular ammonium homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular triglyceride homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular triglyceride homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
sterol homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the sterol homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
potassium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the potassium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
sodium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the sodium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
B-1 B cell homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the B-1 B cell homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
homeostasis of number of cells within a tissue Gene SetFrom GO Biological Process Annotations 2025 genes participating in the homeostasis of number of cells within a tissue biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular monoatomic cation homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular monoatomic cation homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular amino acid homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular amino acid homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of apoptosis involved in tissue homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of apoptosis involved in tissue homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of cell proliferation involved in tissue homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of cell proliferation involved in tissue homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
cartilage homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cartilage homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular chloride ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular chloride ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular manganese ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular manganese ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
Golgi calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the Golgi calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular nitric oxide homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular nitric oxide homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
smooth endoplasmic reticulum calcium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the smooth endoplasmic reticulum calcium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
magnesium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the magnesium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular magnesium ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular magnesium ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
manganese ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the manganese ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
acylglycerol homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the acylglycerol homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular sphingolipid homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular sphingolipid homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
monoatomic cation homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the monoatomic cation homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
monoatomic anion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the monoatomic anion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular monoatomic anion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular monoatomic anion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
Neurotransmitter Regulation and Iron Homeostasis Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Neurotransmitter Regulation and Iron Homeostasis assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Cellular Redox Homeostasis and Vesicular Trafficking Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Cellular Redox Homeostasis and Vesicular Trafficking assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Cellular Ion Homeostasis and Metal Ion Transport Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Cellular Ion Homeostasis and Metal Ion Transport assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Regulation of cellular stress responses and metal ion homeostasis Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Regulation of cellular stress responses and metal ion homeostasis assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Cellular redox homeostasis and nucleotide biosynthesis regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Cellular redox homeostasis and nucleotide biosynthesis regulation assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Homeostasis model assessment of insulin resistance Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of insulin resistance phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Glucose homeostasis traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Glucose homeostasis traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Homeostasis model assessment of beta-cell function (dietary factor interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of beta-cell function (dietary factor interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Homeostasis model assessment of insulin resistance (dietary factor interaction) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of insulin resistance (dietary factor interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Homeostasis model assessment of insulin resistance in less-fat diet Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of insulin resistance in less-fat diet phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Homeostasis model assessment of insulin resistance x saturated fatty acids interaction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of insulin resistance x saturated fatty acids interaction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Homeostasis model assessment of beta-cell function Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Homeostasis model assessment of beta-cell function phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
Hypertelorism with esophageal abnormality and hypospadias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
congenital nervous system abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormality of glucagon secretion Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormality of glucagon secretion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastrin secretion abnormality Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastrin secretion abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cadasil; chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
torsion abnormality; vascular malformations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease torsion abnormality; vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; lymphocytosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
smooth pursuit eye movement abnormality Gene SetFrom GAD Gene-Disease Associations genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormality Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormality in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormality of vitamin metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endometrium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endometrium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forearm bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forearm bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the integument Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the integument phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin d metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of myeloid leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral subcortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral subcortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stomach Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stomach phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycolipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of connective tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of connective tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aortic valve Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cellular immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cellular immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
hearing abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the hearing abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune serum protein physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of leukocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of oral mucosa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of oral mucosa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urethra Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urethra phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of brain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of brain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the endocrine system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the endocrine system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cerebral artery Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cerebral artery phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the breast Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the breast phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the autonomic nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the autonomic nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
eeg abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the eeg abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femur Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femur phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the immune system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin a metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the calf Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the calf phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the carotid arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the carotid arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of retinal arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the kidney Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the kidney phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circle of willis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circle of willis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hand Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hand phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pituitary gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pituitary gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the myocardium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the myocardium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the biliary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the biliary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cell cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cell cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of von willebrand factor Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of long bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thrombocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thrombocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of neutrophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of neutrophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hip bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the iris Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the iris phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lower urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of thyroid physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of hair pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
mesangial abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the mesangial abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin b metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating fibrinogen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating fibrinogen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the adrenal glands Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the adrenal glands phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the respiratory system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of phalanx of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the musculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the musculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral white matter Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the duodenum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the duodenum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull base Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the astrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the astrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of basophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of basophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the face Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the face phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the male genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the male genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of facial skeleton Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of facial skeleton phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the posterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gingiva Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gingiva phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the large intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lung Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lung phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating hormone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating hormone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the placenta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the placenta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ankles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ankles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the heart valves Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the heart valves phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of aromatic amino acid family metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eye movement Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ovary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ovary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the prostate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the prostate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of digit Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of digit phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limbs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the testis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the testis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior segment of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental eruption Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental eruption phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the clavicle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the clavicle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of homocysteine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the knees Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the knees phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coronary arteries Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coronary arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cardiovascular system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cardiovascular system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin adnexa Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pleura Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pleura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of interleukin secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of interleukin secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood and blood-forming tissues Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of tryptophan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of tryptophan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of head or neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of head or neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mandible Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mandible phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional respiratory abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone mineral density Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of humoral immunity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of humoral immunity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
neurodevelopmental abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the neurodevelopmental abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of taste sensation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of taste sensation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of renin-angiotensin system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of renin-angiotensin system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pancreas physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skeletal system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of primary teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thorax Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thorax phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the thyroid gland Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the thyroid gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdomen Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdomen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebrospinal fluid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebrospinal fluid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the menstrual cycle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the menstrual cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
behavioral abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the behavioral abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the oral cavity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the oral cavity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cholesterol metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cholesterol metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of granulocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of granulocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the fundus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the fundus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of forebrain morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of forebrain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the tongue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the tongue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vertebrae Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vertebrae phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the spinal cord Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
vascular skin abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of refraction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of refraction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dna repair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dna repair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nose Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nose phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of central nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of erythrocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of erythrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of liposaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of liposaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the urinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the urinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vasculature of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glomerulus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of unsaturated fatty acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiac morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiac morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating protein level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating protein level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
prenatal maternal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humeral diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humeral diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
phenotypic abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the phenotypic abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uterus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uterus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of female internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the cornea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the metaphyses Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the metaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
functional abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gastrointestinal tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the common coagulation pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fatty-acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genitourinary system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genitourinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cytokine secretion Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cytokine secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
growth abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the growth abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the choroid Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the choroid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the globe Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the globe phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of radial diaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of radial diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear ossicles Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the monocyte/macrophage lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb joint Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the uvea Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the uvea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
biliary tract abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the biliary tract abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the abdominal organs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the abdominal organs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the esophagus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the esophagus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retina Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retina phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the penis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the penis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of blood circulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the radius Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the radius phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the costochondral junction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the costochondral junction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cerebral cortex Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
venous abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the venous abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of extrapyramidal motor function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of bone marrow cell morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the liver Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the liver phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of proteoglycan metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of proteoglycan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of fluid regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of fluid regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pylorus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pylorus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of adipose tissue Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of adipose tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the anterior pituitary Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nasopharynx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nasopharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intervertebral disk Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intervertebral disk phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the stapes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the stapes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the gallbladder Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the gallbladder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the coagulation cascade Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the coagulation cascade phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricle Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of pelvic girdle bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
generalized abnormality of skin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lower limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the left ventricular outflow tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of muscle physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the glial cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the glial cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of dental structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of dental structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper arm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ulna Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ulna phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal endothelium Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal endothelium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lymphocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lymphocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of corneal thickness Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the mouth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the mouth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the vitamin b12 metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the small intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the genital system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the genital system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the aorta Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the aorta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the female genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the female genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the humerus Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the humerus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cardiovascular system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of complement system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of complement system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cells of the erythroid lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
chorioretinal abnormality Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the chorioretinal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of sulfur amino acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of sulfur amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating cortisol level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating cortisol level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of prothrombin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of prothrombin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the curvature of the vertebral column Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the curvature of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of coagulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of coagulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the cervical spine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the cervical spine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the skull Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of carboxylic acid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the middle ear Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the pancreas Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the pancreas phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skeletal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skeletal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the lens Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the lens phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of b cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body weight Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of temperature regulation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of temperature regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the systemic arterial tree Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the systemic arterial tree phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the rib cage Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the rib cage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of glycoprotein metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of vitamin e metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of cell physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the eye Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the retinal vasculature Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of skin pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of skin pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of macrophages Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of macrophages phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of male external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of male external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of body height Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of body height phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of polysaccharide metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of polysaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the intrinsic pathway Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the intrinsic pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of eosinophils Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of eosinophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the macula Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the macula phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of epidermal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of epidermal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of higher mental function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of higher mental function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the ribs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the ribs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of nucleobase metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of nucleobase metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the forearm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the forearm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of purine metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of purine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of serum cytokine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of serum cytokine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of immune system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of immune system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating leptin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating leptin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the nephron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the nephron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of circulating glucocorticoid level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of circulating glucocorticoid level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the level of lipoprotein cholesterol Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the level of lipoprotein cholesterol phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the falx cerebri Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the falx cerebri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of myeloid leukocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of myeloid leukocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of gastrointestinal vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of gastrointestinal vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the extraocular muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choanae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choanae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycolipid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycolipid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal cavity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal cavity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the immune system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the immune system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of reticulocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of reticulocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cochlea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of von willebrand factor Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac ventricle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cerebellar peduncle Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the gingiva Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the gingiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lung Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lung phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the gastrointestinal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the basal ganglia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vena cava Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vena cava phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of sharpey fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of sharpey fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hypothalamus-pituitary axis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hypothalamus-pituitary axis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the cornea Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of metacarpophalangeal joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of metacarpophalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the intrahepatic bile duct Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the intrahepatic bile duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of fluid regulation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of fluid regulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the philtrum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dentate nucleus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fallopian tube Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of secondary sexual hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pineal gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pineal gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the crus of the helix Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the crus of the helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acetabulum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acetabulum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sense of smell Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sense of smell phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of central somatosensory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of permanent molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of permanent molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of muscle physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of muscle physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the parathyroid physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the parathyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the achilles tendon Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the achilles tendon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the myocardium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the myocardium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of complement system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of complement system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the medullary cavity of the long bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of glycoprotein metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of glycoprotein metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of blood glucose concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of blood glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal tubule Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal tubule phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the shoulder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the shoulder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 3rd toe Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of chromosome condensation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prostaglandin metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prostaglandin metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neurodevelopmental abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the neurodevelopmental abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of connective tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of connective tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thumb phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the odontoid process Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alanine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alanine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
atlantoaxial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the atlantoaxial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lower limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lower limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thrombocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thrombocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the posterior pituitary Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the posterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the anterior chamber Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the vestibulocochlear nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the vestibulocochlear nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prenatal development or birth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prenatal development or birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of binocular vision Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of binocular vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nasal septum Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thyroid gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thyroid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the alveolar ridges Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of forebrain morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of forebrain morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cerebral artery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cerebral artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the choroid plexus Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the choroid plexus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating protein level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating protein level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of pancreas morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of pancreas morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the seventh cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the seventh cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the labia minora Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the palmar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
biliary tract abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the biliary tract abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the lymphoid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the lymphoid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized abnormality of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cardiac morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cardiac morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the glial cells Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the glial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the aryepiglottic fold Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the aryepiglottic fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cells of the erythroid lineage Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cells of the erythroid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of prothrombin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of prothrombin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of b cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the subungual region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the subungual region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thyroid morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thyroid morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the scalp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inflammatory abnormality of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the frontal hairline Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the frontal hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the retinal pigment epithelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the renal collecting system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the renal collecting system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pulmonary vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pulmonary vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the middle phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of peripheral nerves Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the acoustic reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the acoustic reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the middle ear Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tubulointerstitial abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the tubulointerstitial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the dental pulp Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the dental pulp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cysteine metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cysteine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the thenar eminence Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of ganglioside metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of ganglioside metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of humoral immunity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of humoral immunity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sixth cranial nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sixth cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of calvarial morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of calvarial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hip joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hip joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the humeral metaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the humeral metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of urine bicarbonate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of urine bicarbonate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the genitourinary system Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the genitourinary system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the lymphatic vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the fascia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the fascia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the ear Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the liver Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the liver phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of dental color Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of dental color phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of alkaline phosphatase activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of alkaline phosphatase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the larynx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the larynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chorioretinal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the chorioretinal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of circulating hormone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of circulating hormone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
morphological abnormality of the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the morphological abnormality of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the salivary glands Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the salivary glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of primary molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of primary molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the sacroiliac joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the sacroiliac joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the diaphragm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of movement Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |