Decreased cranial base ossification

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Results for "Decreased cranial base ossification": 1002 gene sets

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decreased cranial base ossification Gene Set From HPO Gene-Disease Associations genes associated with the decreased cranial base ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Decreased Cranial Base Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Cranial Base Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
base-excision repair, AP site formation via deaminated base removal Gene Set From GO Biological Process Annotations 2023 genes participating in the base-excision repair, AP site formation via deaminated base removal biological process from the curated GO Biological Process Annotations 2023 dataset.
base-excision repair, AP site formation via deaminated base removal Gene Set From GO Biological Process Annotations 2025 genes participating in the base-excision repair, AP site formation via deaminated base removal biological process from the curated GO Biological Process Annotations 2025 dataset.
ossification of posterior longitudinal ligament; ossification, heterotopic Gene Set From GAD Gene-Disease Associations genes associated with the disease ossification of posterior longitudinal ligament; ossification, heterotopic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased cranial neural crest cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cranial neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cranial neural crest cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cranial neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cranial neural crest cell proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cranial neural crest cell proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cranial neural crest cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cranial neural crest cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased calvarial ossification Gene Set From HPO Gene-Disease Associations genes associated with the decreased calvarial ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased skull ossification Gene Set From HPO Gene-Disease Associations genes associated with the decreased skull ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Decreased Calvarial Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Calvarial Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
decreased bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
proteasome regulatory particle, base subcomplex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the proteasome regulatory particle, base subcomplex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cytosolic trna wobble base thiouridylase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytosolic trna wobble base thiouridylase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Bandrowski's base Gene Set From CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Bandrowski's base from the curated CTD Gene-Chemical Interactions dataset.
skull base chordoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skull base chordoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skull base meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skull base meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
skull base neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease skull base neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
base Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term base in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
rrna base methylation Gene Set From GO Biological Process Annotations 2015 genes participating in the rrna base methylation biological process from the curated GO Biological Process Annotations 2015 dataset.
trna wobble base modification Gene Set From GO Biological Process Annotations 2015 genes participating in the trna wobble base modification biological process from the curated GO Biological Process Annotations 2015 dataset.
base conversion or substitution editing Gene Set From GO Biological Process Annotations 2015 genes participating in the base conversion or substitution editing biological process from the curated GO Biological Process Annotations 2015 dataset.
base-excision repair, ap site formation Gene Set From GO Biological Process Annotations 2015 genes participating in the base-excision repair, ap site formation biological process from the curated GO Biological Process Annotations 2015 dataset.
base-excision repair, gap-filling Gene Set From GO Biological Process Annotations 2015 genes participating in the base-excision repair, gap-filling biological process from the curated GO Biological Process Annotations 2015 dataset.
base-excision repair, dna ligation Gene Set From GO Biological Process Annotations 2015 genes participating in the base-excision repair, dna ligation biological process from the curated GO Biological Process Annotations 2015 dataset.
base-excision repair Gene Set From GO Biological Process Annotations 2015 genes participating in the base-excision repair biological process from the curated GO Biological Process Annotations 2015 dataset.
proteasome regulatory particle, base subcomplex Gene Set From GO Cellular Component Annotations 2015 proteins localized to the proteasome regulatory particle, base subcomplex cellular component from the curated GO Cellular Component Annotations 2015 dataset.
ciliary base Gene Set From GO Cellular Component Annotations 2015 proteins localized to the ciliary base cellular component from the curated GO Cellular Component Annotations 2015 dataset.
pyrimidine-specific mismatch base pair dna n-glycosylase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the pyrimidine-specific mismatch base pair dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
oxidized base lesion dna n-glycosylase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the oxidized base lesion dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
mismatch base pair dna n-glycosylase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the mismatch base pair dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
deaminated base dna n-glycosylase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the deaminated base dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
site-specific endodeoxyribonuclease activity, specific for altered base Gene Set From GO Molecular Function Annotations 2015 genes performing the site-specific endodeoxyribonuclease activity, specific for altered base molecular function from the curated GO Molecular Function Annotations 2015 dataset.
purine-specific mismatch base pair dna n-glycosylase activity Gene Set From GO Molecular Function Annotations 2015 genes performing the purine-specific mismatch base pair dna n-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
single base insertion or deletion binding Gene Set From GO Molecular Function Annotations 2015 genes performing the single base insertion or deletion binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
sclerosis of skull base Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sclerosis of skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the skull base Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of acid-base homeostasis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sclerosis of skull base Gene Set From HPO Gene-Disease Associations genes associated with the sclerosis of skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive sclerosis of skull base Gene Set From HPO Gene-Disease Associations genes associated with the progressive sclerosis of skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cleft in skull base Gene Set From HPO Gene-Disease Associations genes associated with the cleft in skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal nasal base Gene Set From HPO Gene-Disease Associations genes associated with the abnormal nasal base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pyramidal skinfold extending from the base to the top of the nails Gene Set From HPO Gene-Disease Associations genes associated with the pyramidal skinfold extending from the base to the top of the nails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the skull base Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
wide nasal base Gene Set From HPO Gene-Disease Associations genes associated with the wide nasal base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thick skull base Gene Set From HPO Gene-Disease Associations genes associated with the thick skull base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of acid-base homeostasis Gene Set From 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.
Skull Base Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Skull Base Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Helix-turn-helix, base-excision DNA repair, C-terminal Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Helix-turn-helix, base-excision DNA repair, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Schiff base-forming aldolase, active site Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Schiff base-forming aldolase, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.
abnormal base-excision repair Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal base-excision repair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Base-free sugar-phosphate removal via the single-nucleotide replacement pathway Gene Set From Reactome Pathways 2014 proteins participating in the Base-free sugar-phosphate removal via the single-nucleotide replacement pathway pathway from the Reactome Pathways dataset.
Base-Excision Repair, AP Site Formation Gene Set From Reactome Pathways 2014 proteins participating in the Base-Excision Repair, AP Site Formation pathway from the Reactome Pathways dataset.
Base Excision Repair Gene Set From Reactome Pathways 2014 proteins participating in the Base Excision Repair pathway from the Reactome Pathways dataset.
leaf base Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue leaf base in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
shoot base Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue shoot base in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Skull Base Chordoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Skull Base Chordoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pyramidal Skinfold Extending From The Base To The Top Of The Nails Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pyramidal Skinfold Extending From The Base To The Top Of The Nails in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Skull Base Meningioma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Skull Base Meningioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Skull Base Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Carcinoma Of Base Of Tongue Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Carcinoma Of Base Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Wide Nasal Base Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Nasal Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Narrow Nasal Base Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Narrow Nasal Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thick Skull Base Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cleft In Skull Base Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cleft In Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Sclerosis Of Skull Base Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Sclerosis Of Skull Base in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
rRNA base methylation Gene Set From GO Biological Process Annotations 2023 genes participating in the rRNA base methylation biological process from the curated GO Biological Process Annotations 2023 dataset.
base-excision repair Gene Set From GO Biological Process Annotations 2023 genes participating in the base-excision repair biological process from the curated GO Biological Process Annotations 2023 dataset.
base-excision repair, gap-filling Gene Set From GO Biological Process Annotations 2023 genes participating in the base-excision repair, gap-filling biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of base-excision repair Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of base-excision repair biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of base-excision repair Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of base-excision repair biological process from the curated GO Biological Process Annotations 2023 dataset.
telomere maintenance via base-excision repair Gene Set From GO Biological Process Annotations 2023 genes participating in the telomere maintenance via base-excision repair biological process from the curated GO Biological Process Annotations 2023 dataset.
base-excision repair, AP site formation Gene Set From GO Biological Process Annotations 2023 genes participating in the base-excision repair, AP site formation biological process from the curated GO Biological Process Annotations 2023 dataset.
base-excision repair, DNA ligation Gene Set From GO Biological Process Annotations 2023 genes participating in the base-excision repair, DNA ligation biological process from the curated GO Biological Process Annotations 2023 dataset.
base conversion or substitution editing Gene Set From GO Biological Process Annotations 2023 genes participating in the base conversion or substitution editing biological process from the curated GO Biological Process Annotations 2023 dataset.
tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation Gene Set From GO Biological Process Annotations 2023 genes participating in the tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation biological process from the curated GO Biological Process Annotations 2023 dataset.
tRNA wobble base cytosine methylation Gene Set From GO Biological Process Annotations 2023 genes participating in the tRNA wobble base cytosine methylation biological process from the curated GO Biological Process Annotations 2023 dataset.
tRNA wobble base modification Gene Set From GO Biological Process Annotations 2023 genes participating in the tRNA wobble base modification biological process from the curated GO Biological Process Annotations 2023 dataset.
pyrimidine-specific mismatch base pair DNA N-glycosylase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the pyrimidine-specific mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
purine-specific mismatch base pair DNA N-glycosylase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the purine-specific mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
site-specific endodeoxyribonuclease activity, specific for altered base Gene Set From GO Molecular Function Annotations 2023 genes performing the site-specific endodeoxyribonuclease activity, specific for altered base molecular function from the curated GO Molecular Function Annotations 2023 dataset.
single base insertion or deletion binding Gene Set From GO Molecular Function Annotations 2023 genes performing the single base insertion or deletion binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.
oxidized base lesion DNA N-glycosylase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the oxidized base lesion DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
mismatch base pair DNA N-glycosylase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
deaminated base DNA N-glycosylase activity Gene Set From GO Molecular Function Annotations 2023 genes performing the deaminated base DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.
abnormal base-excision repair Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal base-excision repair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Crypt-base columnar cell_Intestine_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Crypt-base columnar cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Crypt base columnar(CBC) cell_Intestine_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Crypt base columnar(CBC) cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Base excision repair Gene Set From WikiPathways Pathways 2024 proteins participating in the Base excision repair pathway from the WikiPathways Pathways 2024 dataset.
Base Excision Repair Gene Set From Reactome Pathways 2024 proteins participating in the Base Excision Repair pathway from the Reactome Pathways 2024 dataset.
Base-Excision Repair, AP Site Formation Gene Set From Reactome Pathways 2024 proteins participating in the Base-Excision Repair, AP Site Formation pathway from the Reactome Pathways 2024 dataset.
Defective Base Excision Repair Associated with MUTYH Gene Set From Reactome Pathways 2024 proteins participating in the Defective Base Excision Repair Associated with MUTYH pathway from the Reactome Pathways 2024 dataset.
Defective Base Excision Repair Associated with NEIL1 Gene Set From Reactome Pathways 2024 proteins participating in the Defective Base Excision Repair Associated with NEIL1 pathway from the Reactome Pathways 2024 dataset.
Defective Base Excision Repair Associated with NEIL3 Gene Set From Reactome Pathways 2024 proteins participating in the Defective Base Excision Repair Associated with NEIL3 pathway from the Reactome Pathways 2024 dataset.
Defective Base Excision Repair Associated with NTHL1 Gene Set From Reactome Pathways 2024 proteins participating in the Defective Base Excision Repair Associated with NTHL1 pathway from the Reactome Pathways 2024 dataset.
Defective Base Excision Repair Associated with OGG1 Gene Set From Reactome Pathways 2024 proteins participating in the Defective Base Excision Repair Associated with OGG1 pathway from the Reactome Pathways 2024 dataset.
Diseases of Base Excision Repair Gene Set From Reactome Pathways 2024 proteins participating in the Diseases of Base Excision Repair pathway from the Reactome Pathways 2024 dataset.
PCNA-Dependent Long Patch Base Excision Repair Gene Set From Reactome Pathways 2024 proteins participating in the PCNA-Dependent Long Patch Base Excision Repair pathway from the Reactome Pathways 2024 dataset.
POLB-Dependent Long Patch Base Excision Repair Gene Set From Reactome Pathways 2024 proteins participating in the POLB-Dependent Long Patch Base Excision Repair pathway from the Reactome Pathways 2024 dataset.
rRNA base methylation Gene Set From GO Biological Process Annotations 2025 genes participating in the rRNA base methylation biological process from the curated GO Biological Process Annotations 2025 dataset.
base-excision repair Gene Set From GO Biological Process Annotations 2025 genes participating in the base-excision repair biological process from the curated GO Biological Process Annotations 2025 dataset.
base-excision repair, gap-filling Gene Set From GO Biological Process Annotations 2025 genes participating in the base-excision repair, gap-filling biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of base-excision repair Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of base-excision repair biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of base-excision repair Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of base-excision repair biological process from the curated GO Biological Process Annotations 2025 dataset.
telomere maintenance via base-excision repair Gene Set From GO Biological Process Annotations 2025 genes participating in the telomere maintenance via base-excision repair biological process from the curated GO Biological Process Annotations 2025 dataset.
base-excision repair, AP site formation Gene Set From GO Biological Process Annotations 2025 genes participating in the base-excision repair, AP site formation biological process from the curated GO Biological Process Annotations 2025 dataset.
base conversion or substitution editing Gene Set From GO Biological Process Annotations 2025 genes participating in the base conversion or substitution editing biological process from the curated GO Biological Process Annotations 2025 dataset.
tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation Gene Set From GO Biological Process Annotations 2025 genes participating in the tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation biological process from the curated GO Biological Process Annotations 2025 dataset.
tRNA wobble base cytosine methylation Gene Set From GO Biological Process Annotations 2025 genes participating in the tRNA wobble base cytosine methylation biological process from the curated GO Biological Process Annotations 2025 dataset.
tRNA wobble base modification Gene Set From GO Biological Process Annotations 2025 genes participating in the tRNA wobble base modification biological process from the curated GO Biological Process Annotations 2025 dataset.
pyrimidine-specific mismatch base pair DNA N-glycosylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the pyrimidine-specific mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
purine-specific mismatch base pair DNA N-glycosylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the purine-specific mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
site-specific endodeoxyribonuclease activity, specific for altered base Gene Set From GO Molecular Function Annotations 2025 genes performing the site-specific endodeoxyribonuclease activity, specific for altered base molecular function from the curated GO Molecular Function Annotations 2025 dataset.
single base insertion or deletion binding Gene Set From GO Molecular Function Annotations 2025 genes performing the single base insertion or deletion binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.
oxidized base lesion DNA N-glycosylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the oxidized base lesion DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
mismatch base pair DNA N-glycosylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the mismatch base pair DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
deaminated base DNA N-glycosylase activity Gene Set From GO Molecular Function Annotations 2025 genes performing the deaminated base DNA N-glycosylase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.
Skull base meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skull base meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Skull base cancer Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skull base cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Skull base chordoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Skull base chordoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Leaf base Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Leaf base in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Shoot base Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Shoot base in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Ciliary base Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Ciliary base cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Stereocilium base Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Stereocilium base cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Proteasome regulatory particle, base subcomplex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proteasome regulatory particle, base subcomplex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Cytosolic tRNA wobble base thiouridylase complex Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cytosolic tRNA wobble base thiouridylase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Ciliary base Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Ciliary base cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Mating projection base Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Mating projection base cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Stereocilium base Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Stereocilium base cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Cytosolic tRNA wobble base thiouridylase complex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cytosolic tRNA wobble base thiouridylase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Phagocytic cup base Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Phagocytic cup base cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Proteasome regulatory particle, base subcomplex Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Proteasome regulatory particle, base subcomplex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Base excision repair Gene Set From KEGG Pathways 2026 proteins participating in the Base excision repair pathway from the KEGG Pathways 2026 dataset.
SEL120-34A FREE BASE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the SEL120-34A FREE BASE drug from theDGIdb Drug Targets 2026 dataset.
CEFAMANDOLE NAFATE FREE BASE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the CEFAMANDOLE NAFATE FREE BASE drug from theDGIdb Drug Targets 2026 dataset.
DS-3801B FREE BASE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the DS-3801B FREE BASE drug from theDGIdb Drug Targets 2026 dataset.
AV-412 FREE BASE Gene Set From DGIdb Drug Targets 2026 interacting proteins for the AV-412 FREE BASE drug from theDGIdb Drug Targets 2026 dataset.
Osteopathia striata with cranial sclerosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Osteopathia striata with cranial sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Synovitis granulomatous with uveitis and cranial neuropathies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Synovitis granulomatous with uveitis and cranial neuropathies from the curated CTD Gene-Disease Associations dataset.
Osteopathia striata cranial sclerosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Osteopathia striata cranial sclerosis from the curated CTD Gene-Disease Associations dataset.
Cranial Nerve Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cranial Nerve Diseases from the curated CTD Gene-Disease Associations dataset.
cranial nerve disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cranial nerve disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cranial nerve malignant neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cranial nerve malignant neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
fourth cranial nerve palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease fourth cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
schwannoma of twelfth cranial nerve Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease schwannoma of twelfth cranial nerve in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cranial nerve palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
anterior cranial fossa meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease anterior cranial fossa meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cranial nerve neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cranial nerve neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
multiple cranial nerve palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease multiple cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cranial nerve disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cranial nerve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
third cranial nerve disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease third cranial nerve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
posterior cranial fossa meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease posterior cranial fossa meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cranial Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cranial in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cranial ganglion development Gene Set From GO Biological Process Annotations 2015 genes participating in the cranial ganglion development biological process from the curated GO Biological Process Annotations 2015 dataset.
cranial nerve morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cranial nerve morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
cranial nerve formation Gene Set From GO Biological Process Annotations 2015 genes participating in the cranial nerve formation biological process from the curated GO Biological Process Annotations 2015 dataset.
cranial nerve development Gene Set From GO Biological Process Annotations 2015 genes participating in the cranial nerve development biological process from the curated GO Biological Process Annotations 2015 dataset.
cranial nerve structural organization Gene Set From GO Biological Process Annotations 2015 genes participating in the cranial nerve structural organization biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic cranial skeleton morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic cranial skeleton morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
cranial suture morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cranial suture morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
cranial nerve disease Gene Set From GWASdb SNP-Disease Associations genes associated with the disease cranial nerve disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
cranial hyperostosis Gene Set From HPO Gene-Disease Associations genes associated with the cranial hyperostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sclerotic cranial sutures Gene Set From HPO Gene-Disease Associations genes associated with the sclerotic cranial sutures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the seventh cranial nerve Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the seventh cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the sixth cranial nerve Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the sixth cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cranial nerve compression Gene Set From HPO Gene-Disease Associations genes associated with the cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed cranial suture closure Gene Set From HPO Gene-Disease Associations genes associated with the delayed cranial suture closure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
wide cranial sutures Gene Set From HPO Gene-Disease Associations genes associated with the wide cranial sutures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
paraganglioma-related cranial nerve palsy Gene Set From HPO Gene-Disease Associations genes associated with the paraganglioma-related cranial nerve palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of cranial sutures Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of cranial sutures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
facial palsy secondary to cranial hyperostosis Gene Set From HPO Gene-Disease Associations genes associated with the facial palsy secondary to cranial hyperostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the fontanelles or cranial sutures Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the fontanelles or cranial sutures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cranial nerve motor loss Gene Set From HPO Gene-Disease Associations genes associated with the cranial nerve motor loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cranial nerve paralysis Gene Set From HPO Gene-Disease Associations genes associated with the cranial nerve paralysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
optic atrophy from cranial nerve compression Gene Set From HPO Gene-Disease Associations genes associated with the optic atrophy from cranial nerve compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the posterior cranial fossa Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the posterior cranial fossa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cranial asymmetry Gene Set From HPO Gene-Disease Associations genes associated with the cranial asymmetry phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the cranial nerves Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cranial nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal cranial neural crest cell migration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cranial neural crest cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ectopic cranial bone growth Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ectopic cranial bone growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cranial neural crest cell apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cranial neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cranial vagina morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cranial vagina morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cranial vagina Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cranial vagina phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cranial neural crest cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cranial neural crest cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cranial flexure morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cranial flexure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cranial suture morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cranial suture morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cranial neural crest cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cranial neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cranial nerve morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cranial nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cranial ganglia morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cranial ganglia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
osteopathia striata with cranial sclerosis Gene Set From OMIM Gene-Disease Associations genes associated with the osteopathia striata with cranial sclerosis phenotype from the curated OMIM Gene-Disease Associations dataset.
cranial nerve Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cranial nerve in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
cranial ganglion Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue cranial ganglion in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.
cranial nerve Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cranial nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cranial ganglion Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cranial ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Synovitis, Granulomatous, With Uveitis And Cranial Neuropathies (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Synovitis, Granulomatous, With Uveitis And Cranial Neuropathies (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fourth Cranial Nerve Paresis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fourth Cranial Nerve Paresis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Osteopathia Striata Cranial Sclerosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Osteopathia Striata Cranial Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cranial Nerve Palsies Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cranial Nerve Palsies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Fontanelles Or Cranial Sutures Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Fontanelles Or Cranial Sutures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Cranial Nerves Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Cranial Nerves in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cranial Fasciitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cranial Fasciitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cranial Nerve Compression Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cranial Nerve Compression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cranial Arteritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cranial Arteritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cranial Neuropathies, Multiple Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cranial Neuropathies, Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Cranial Nerve Palsy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Cranial Nerve Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Wide Cranial Sutures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Cranial Sutures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Posterior Cranial Fossa Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Posterior Cranial Fossa in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cranial Hyperostosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cranial Hyperostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cranial Asymmetry Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cranial Asymmetry in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Eleventh Cranial Nerve Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Eleventh Cranial Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Twelfth Cranial Nerve Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Twelfth Cranial Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Sclerotic Cranial Sutures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sclerotic Cranial Sutures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Ridged Cranial Sutures Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ridged Cranial Sutures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cranial Nerve Motor Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cranial Nerve Motor Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Facial Palsy Secondary To Cranial Hyperostosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Palsy Secondary To Cranial Hyperostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
embryonic cranial skeleton morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the embryonic cranial skeleton morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
cranial nerve development Gene Set From GO Biological Process Annotations 2023 genes participating in the cranial nerve development biological process from the curated GO Biological Process Annotations 2023 dataset.
cranial suture morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the cranial suture morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
cranial nerve maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the cranial nerve maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
cranial ganglion development Gene Set From GO Biological Process Annotations 2023 genes participating in the cranial ganglion development biological process from the curated GO Biological Process Annotations 2023 dataset.
ectopic cranial bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ectopic cranial bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial ganglia morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial ganglia morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial flexure morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial flexure morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial nerve morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial nerve morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial neural crest cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial neural crest cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
wide cranial sutures Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the wide cranial sutures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
premature cranial suture closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the premature cranial suture closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cranial vagina Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cranial vagina phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed cranial suture closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed cranial suture closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial suture morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial suture morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial neural crest cell migration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial neural crest cell migration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
large cranial foramen ovale Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the large cranial foramen ovale phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
premature cranial synchondrosis closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the premature cranial synchondrosis closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small cranial cavity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small cranial cavity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial vertex morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial vertex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial cavity morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial cavity morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased cranial neural crest cell apoptosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cranial neural crest cell apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cranial bossing Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cranial bossing phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial cartilage morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial cartilage morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial foramen morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial foramen morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired cranial neural crest cell differentiation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired cranial neural crest cell differentiation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal posterior cranial fossa morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal posterior cranial fossa morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial cartilage development Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial cartilage development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial blood vasculature morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial blood vasculature morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cranial synchondrosis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cranial synchondrosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Cranial mesoderm cell_Heart_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Cranial mesoderm cell_Heart_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early cranial neural crest cell_Soft palate_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early cranial neural crest cell_Soft palate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Cranial neural crest-derived mesenchymal cell_Soft palate_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Cranial neural crest-derived mesenchymal cell_Soft palate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Cranial neural crest cell_Skin_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Cranial neural crest cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Cranial neural crest-derived mesenchymal cell_Skin_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Cranial neural crest-derived mesenchymal cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
embryonic cranial skeleton morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the embryonic cranial skeleton morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
cranial nerve development Gene Set From GO Biological Process Annotations 2025 genes participating in the cranial nerve development biological process from the curated GO Biological Process Annotations 2025 dataset.
cranial suture morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the cranial suture morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
cranial nerve maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the cranial nerve maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
cranial ganglion development Gene Set From GO Biological Process Annotations 2025 genes participating in the cranial ganglion development biological process from the curated GO Biological Process Annotations 2025 dataset.
Cranial nerve disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cranial nerve disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cranial nerve disease Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Cranial nerve disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Cranial nerve disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cranial nerve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Third cranial nerve disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Third cranial nerve disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cranial nerve palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multiple cranial nerve palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multiple cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cranial nerve malignant neoplasm Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cranial nerve malignant neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Fourth cranial nerve palsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Fourth cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Osteopathia striata with cranial sclerosis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Osteopathia striata with cranial sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurilemmoma of the fifth cranial nerve Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurilemmoma of the fifth cranial nerve in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Schwannoma of twelfth cranial nerve Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Schwannoma of twelfth cranial nerve in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Anterior cranial fossa meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Anterior cranial fossa meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Middle cranial fossa meningioma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Middle cranial fossa meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cranial nerve III tumor Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cranial nerve III tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cranial nerve Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cranial nerve in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Cranial ganglion Gene Set From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Cranial ganglion in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.
Cranial nerve Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cranial nerve in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cranial ganglion Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cranial ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Obesity in adult survivors of childhood cancer exposed to cranial radiation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obesity in adult survivors of childhood cancer exposed to cranial radiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Obesity in adult survivors of childhood cancer not exposed to cranial radiation Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Obesity in adult survivors of childhood cancer not exposed to cranial radiation phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Ossification of the posterior longitudinal ligament of the spine Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ossification of the posterior longitudinal ligament of the spine from the curated CTD Gene-Disease Associations dataset.
Ossification, Heterotopic Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Ossification, Heterotopic from the curated CTD Gene-Disease Associations dataset.
ossification of the posterior longitudinal ligament of the spine Gene Set From GAD Gene-Disease Associations genes associated with the disease ossification of the posterior longitudinal ligament of the spine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ossification of the posterior longitudinal ligament Gene Set From GAD Gene-Disease Associations genes associated with the disease ossification of the posterior longitudinal ligament in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ossification of the posterior longitudinal ligament of the spine (opll) Gene Set From GAD Gene-Disease Associations genes associated with the disease ossification of the posterior longitudinal ligament of the spine (opll) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ossification of spine Gene Set From GAD Gene-Disease Associations genes associated with the disease ossification of spine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; ossification of posterior longitudinal ligament Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; ossification of posterior longitudinal ligament in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome Gene Set From GAD Gene-Disease Associations genes associated with the disease bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hyperostosis; ossification of posterior longitudinal ligament; spondylitis, ankylosing; uveitis Gene Set From GAD Gene-Disease Associations genes associated with the disease hyperostosis; ossification of posterior longitudinal ligament; spondylitis, ankylosing; uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ossification of posterior longitudinal ligament Gene Set From GAD Gene-Disease Associations genes associated with the disease ossification of posterior longitudinal ligament in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal ossification Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal ossification in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ossification Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term ossification in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
ossification involved in bone remodeling Gene Set From GO Biological Process Annotations 2015 genes participating in the ossification involved in bone remodeling biological process from the curated GO Biological Process Annotations 2015 dataset.
direct ossification Gene Set From GO Biological Process Annotations 2015 genes participating in the direct ossification biological process from the curated GO Biological Process Annotations 2015 dataset.
endochondral ossification Gene Set From GO Biological Process Annotations 2015 genes participating in the endochondral ossification biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of ossification Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of ossification biological process from the curated GO Biological Process Annotations 2015 dataset.
replacement ossification Gene Set From GO Biological Process Annotations 2015 genes participating in the replacement ossification biological process from the curated GO Biological Process Annotations 2015 dataset.
ossification Gene Set From GO Biological Process Annotations 2015 genes participating in the ossification biological process from the curated GO Biological Process Annotations 2015 dataset.
ossification involved in bone maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the ossification involved in bone maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
intramembranous ossification Gene Set From GO Biological Process Annotations 2015 genes participating in the intramembranous ossification biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of ossification Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of ossification biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of ossification Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of ossification biological process from the curated GO Biological Process Annotations 2015 dataset.
abnormal ossification of hand bones Gene Set From HPO Gene-Disease Associations genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent sternal ossification Gene Set From HPO Gene-Disease Associations genes associated with the absent sternal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
irregular ossification at anterior rib ends Gene Set From HPO Gene-Disease Associations genes associated with the irregular ossification at anterior rib ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal enchondral ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal enchondral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
two carpal ossification centers present at birth Gene Set From HPO Gene-Disease Associations genes associated with the two carpal ossification centers present at birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fused sternal ossification centers Gene Set From HPO Gene-Disease Associations genes associated with the fused sternal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal humeral ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal humeral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed tarsal ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cartilaginous ossification of larynx Gene Set From HPO Gene-Disease Associations genes associated with the cartilaginous ossification of larynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multicentric ossification of proximal femoral epiphyses Gene Set From HPO Gene-Disease Associations genes associated with the multicentric ossification of proximal femoral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multicentric ossification of proximal humeral epiphyses Gene Set From HPO Gene-Disease Associations genes associated with the multicentric ossification of proximal humeral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
severe carpal ossification delay Gene Set From HPO Gene-Disease Associations genes associated with the severe carpal ossification delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal tarsal ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ectopic ossification in ligament tissue Gene Set From HPO Gene-Disease Associations genes associated with the ectopic ossification in ligament tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of skull ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of skull ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
advanced ossification of carpal bones Gene Set From HPO Gene-Disease Associations genes associated with the advanced ossification of carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of carpal bone ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of carpal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed patellar ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed patellar ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed femoral head ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed femoral head ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
large sternal ossification centers Gene Set From HPO Gene-Disease Associations genes associated with the large sternal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent in utero rib ossification Gene Set From HPO Gene-Disease Associations genes associated with the absent in utero rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal metatarsal ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal metatarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal pelvis bone ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal pelvis bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ectopic ossification in muscle tissue Gene Set From HPO Gene-Disease Associations genes associated with the ectopic ossification in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal ossification of the pubic bone Gene Set From HPO Gene-Disease Associations genes associated with the abnormal ossification of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cartilaginous ossification of nose Gene Set From HPO Gene-Disease Associations genes associated with the cartilaginous ossification of nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed phalangeal epiphyseal ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed phalangeal epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
irregular ossification of hand bones Gene Set From HPO Gene-Disease Associations genes associated with the irregular ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal ossification involving the femoral head and neck Gene Set From HPO Gene-Disease Associations genes associated with the abnormal ossification involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal epiphyseal ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed ossification of pubic rami Gene Set From HPO Gene-Disease Associations genes associated with the delayed ossification of pubic rami phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
advanced tarsal ossification Gene Set From HPO Gene-Disease Associations genes associated with the advanced tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed pubic bone ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed pubic bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased skull ossification Gene Set From HPO Gene-Disease Associations genes associated with the increased skull ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
irregular ossification of the humeral epiphyses Gene Set From HPO Gene-Disease Associations genes associated with the irregular ossification of the humeral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
irregular tarsal ossification Gene Set From HPO Gene-Disease Associations genes associated with the irregular tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ectopic ossification in tendon tissue Gene Set From HPO Gene-Disease Associations genes associated with the ectopic ossification in tendon tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal vertebral ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal vertebral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent in utero ossification of vertebral bodies Gene Set From HPO Gene-Disease Associations genes associated with the absent in utero ossification of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple carpal ossification centers Gene Set From HPO Gene-Disease Associations genes associated with the multiple carpal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal bone ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
supernumerary vertebral ossification centers Gene Set From HPO Gene-Disease Associations genes associated with the supernumerary vertebral ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed ossification of carpal bones Gene Set From HPO Gene-Disease Associations genes associated with the delayed ossification of carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed calcaneal ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed calcaneal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal foot bone ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal foot bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal hand bone ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multicentric femoral head ossification Gene Set From HPO Gene-Disease Associations genes associated with the multicentric femoral head ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ectopic ossification Gene Set From HPO Gene-Disease Associations genes associated with the ectopic ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal rib ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal sternal ossification Gene Set From HPO Gene-Disease Associations genes associated with the abnormal sternal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
delayed epiphyseal ossification Gene Set From HPO Gene-Disease Associations genes associated with the delayed epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Ossification of Posterior Longitudinal Ligament Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Ossification of Posterior Longitudinal Ligament phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
abnormal intramembranous bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
failure of bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the failure of bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
failure of endochondral bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the failure of endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal ossification involved in bone maturation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ossification involved in bone maturation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
failure of sternum ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the failure of sternum ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
premature intramembranous bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the premature intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
premature bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the premature bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal long bone epiphyseal ossification zone morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphyseal ossification zone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed endochondral bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sternum ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sternum ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
impaired ossification of basisphenoid bone Gene Set From MPO Gene-Phenotype Associations gene mutations causing the impaired ossification of basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
premature endochondral bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the premature endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal endochondral bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal endochondral bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed intramembranous bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
failure of intramembranous bone ossification Gene Set From MPO Gene-Phenotype Associations gene mutations causing the failure of intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Endochondral Ossification(Homo sapiens) Gene Set From WikiPathways Pathways 2014 proteins participating in the Endochondral Ossification(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.
Endochondral Ossification(Mus musculus) Gene Set From WikiPathways Pathways 2014 proteins participating in the Endochondral Ossification(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.
Ectopic Ossification Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ectopic Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Bone Ossification Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ossification Of The Posterior Longitudinal Ligament Of Spine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ossification Of The Posterior Longitudinal Ligament Of Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absent Ossification Of Calvaria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absent Ossification Of Calvaria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Enchondral Ossification Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Enchondral Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Pelvis Bone Ossification Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Pelvis Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormal Foot Bone Ossification Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Foot Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Supernumerary Vertebral Ossification Centers Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Supernumerary Vertebral Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ectopic Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ectopic Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Advanced Ossification Of Carpal Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Advanced Ossification Of Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Proximal Femoral Epiphyseal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Proximal Femoral Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Ossification Of Carpal Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Ossification Of Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent In Utero Ossification Of Vertebral Bodies Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent In Utero Ossification Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent In Utero Rib Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent In Utero Rib Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Heterotopic Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Heterotopic Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Advanced Tarsal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Advanced Tarsal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fused Sternal Ossification Centers Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fused Sternal Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Carpal Ossification Centers Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Carpal Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Epiphyseal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Calcaneal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Calcaneal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Pubic Bone Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Pubic Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Sternal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Sternal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Early Ossification Of Capital Femoral Epiphyses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Ossification Of Capital Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Epiphyseal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Irregular Ossification At Anterior Rib Ends Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Irregular Ossification At Anterior Rib Ends in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Femoral Head Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Femoral Head Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multicentric Femoral Head Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Femoral Head Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multicentric Ossification Of Proximal Femoral Epiphyses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Ossification Of Proximal Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multicentric Ossification Of Proximal Humeral Epiphyses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Ossification Of Proximal Humeral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Irregular Tarsal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Irregular Tarsal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Incomplete Ossification Of Pubis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Incomplete Ossification Of Pubis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Sternal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Sternal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Hand Bone Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Hand Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Ossification Involving The Femoral Head And Neck Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Ossification Involving The Femoral Head And Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Two Carpal Ossification Centers Present At Birth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Two Carpal Ossification Centers Present At Birth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Ossification Of Pubic Rami Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Ossification Of Pubic Rami in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Tarsal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Tarsal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Patellar Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Patellar Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Phalangeal Epiphyseal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Phalangeal Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cartilaginous Ossification Of Larynx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cartilaginous Ossification Of Larynx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cartilaginous Ossification Of Nose Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cartilaginous Ossification Of Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Large Sternal Ossification Centers Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Sternal Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Irregular Ossification Of Hand Bones Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Irregular Ossification Of Hand Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Severe Carpal Ossification Delay Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Severe Carpal Ossification Delay in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
endochondral ossification Gene Set From GO Biological Process Annotations 2023 genes participating in the endochondral ossification biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of ossification Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of ossification biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of ossification Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of ossification biological process from the curated GO Biological Process Annotations 2023 dataset.
regulation of ossification Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of ossification biological process from the curated GO Biological Process Annotations 2023 dataset.
intramembranous ossification Gene Set From GO Biological Process Annotations 2023 genes participating in the intramembranous ossification biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal sternum ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sternum ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal long bone epiphyseal ossification zone morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphyseal ossification zone morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
impaired ossification of basisphenoid bone Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the impaired ossification of basisphenoid bone phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed endochondral bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed endochondral bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal endochondral bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal endochondral bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal intramembranous bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed intramembranous bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed intramembranous bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
premature bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the premature bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
failure of bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the failure of bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
premature endochondral bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the premature endochondral bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
premature intramembranous bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the premature intramembranous bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
failure of sternum ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the failure of sternum ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
failure of endochondral bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the failure of endochondral bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
failure of intramembranous bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the failure of intramembranous bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal palatal shelf bone ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal palatal shelf bone ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal ossification involved in bone maturation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ossification involved in bone maturation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal perichondrial ossification Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal perichondrial ossification phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Endochondral ossification Gene Set From WikiPathways Pathways 2024 proteins participating in the Endochondral ossification pathway from the WikiPathways Pathways 2024 dataset.
Endochondral ossification with skeletal dysplasias Gene Set From WikiPathways Pathways 2024 proteins participating in the Endochondral ossification with skeletal dysplasias pathway from the WikiPathways Pathways 2024 dataset.
endochondral ossification Gene Set From GO Biological Process Annotations 2025 genes participating in the endochondral ossification biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of ossification Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of ossification biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of ossification Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of ossification biological process from the curated GO Biological Process Annotations 2025 dataset.
regulation of ossification Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of ossification biological process from the curated GO Biological Process Annotations 2025 dataset.
intramembranous ossification Gene Set From GO Biological Process Annotations 2025 genes participating in the intramembranous ossification biological process from the curated GO Biological Process Annotations 2025 dataset.
Ossification of the posterior longitudinal ligament of spine Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Ossification of the posterior longitudinal ligament of spine in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Ossification of the posterior longitudinal ligament of spine Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ossification of the posterior longitudinal ligament of spine in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ossification of the posterior longitudinal ligament of the spine Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Ossification of the posterior longitudinal ligament of the spine phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Kallikrein, decreased urinary activity of Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Kallikrein, decreased urinary activity of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset.
decreased risk of insulin resistance Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased risk of insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased apoptotic level Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased apoptotic level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
neoplasms; decreased cancer risk Gene Set From GAD Gene-Disease Associations genes associated with the disease neoplasms; decreased cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased levels of insulin-receptor messenger ribonucleic acid Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased levels of insulin-receptor messenger ribonucleic acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased fracture risk Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased fracture risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased circulating c4 and predominant mesangial c4 deposition Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased circulating c4 and predominant mesangial c4 deposition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased airway responsiveness Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased airway responsiveness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased chemosensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased chemosensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased glutathione production. Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased glutathione production. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased risk of cerebrovascular mortality Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased risk of cerebrovascular mortality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased lung function Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased lung function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased adipocyte lipolytic function Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased adipocyte lipolytic function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased lung cancer risk Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased lung cancer risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased apoptosis. Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased apoptosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased blood pressure and plasma triglycerides Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased blood pressure and plasma triglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adenoviral infection and decreased lung function Gene Set From GAD Gene-Disease Associations genes associated with the disease adenoviral infection and decreased lung function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
increased concentration of hdl-c and decreased promoter activity Gene Set From GAD Gene-Disease Associations genes associated with the disease increased concentration of hdl-c and decreased promoter activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased bone mass in patients Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased bone mass in patients in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased production rate of apolipoprotein a-i Gene Set From GAD Gene-Disease Associations genes associated with the disease decreased production rate of apolipoprotein a-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
decreased Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term decreased in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
cellular response to decreased oxygen levels Gene Set From GO Biological Process Annotations 2015 genes participating in the cellular response to decreased oxygen levels biological process from the curated GO Biological Process Annotations 2015 dataset.
response to decreased oxygen levels Gene Set From GO Biological Process Annotations 2015 genes participating in the response to decreased oxygen levels biological process from the curated GO Biological Process Annotations 2015 dataset.
decreased body weight Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased fertility Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased fertility phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased corneal thickness Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased liver function Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased liver function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased serum ceruloplasmin Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased serum ceruloplasmin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased testosterone in males Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased testosterone in males phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased pulmonary function Gene Set From GWASdb SNP-Phenotype Associations genes associated with the decreased pulmonary function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
decreased glucosephosphate isomerase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased glucosephosphate isomerase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased facial expression Gene Set From HPO Gene-Disease Associations genes associated with the decreased facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased circulating aldosterone level Gene Set From HPO Gene-Disease Associations genes associated with the decreased circulating aldosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased circulating cortisol level Gene Set From HPO Gene-Disease Associations genes associated with the decreased circulating cortisol level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased cervical spine flexion due to contractures of posterior cervical muscles Gene Set From HPO Gene-Disease Associations genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased adipose tissue around neck Gene Set From HPO Gene-Disease Associations genes associated with the decreased adipose tissue around neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial complex ii Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial complex ii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial complex iv Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial complex iv phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased muscle mass Gene Set From HPO Gene-Disease Associations genes associated with the decreased muscle mass phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased fertility Gene Set From HPO Gene-Disease Associations genes associated with the decreased fertility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased urinary sulfate Gene Set From HPO Gene-Disease Associations genes associated with the decreased urinary sulfate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased adenosylcobalamin Gene Set From HPO Gene-Disease Associations genes associated with the decreased adenosylcobalamin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased fertility in females Gene Set From HPO Gene-Disease Associations genes associated with the decreased fertility in females phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased csf homovanillic acid (hva) Gene Set From HPO Gene-Disease Associations genes associated with the decreased csf homovanillic acid (hva) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of nadph oxidase Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of nadph oxidase phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased nerve conduction velocity Gene Set From HPO Gene-Disease Associations genes associated with the decreased nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of sweat glands Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased t cell activation Gene Set From HPO Gene-Disease Associations genes associated with the decreased t cell activation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased palmar creases Gene Set From HPO Gene-Disease Associations genes associated with the decreased palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased numbers of nephrons Gene Set From HPO Gene-Disease Associations genes associated with the decreased numbers of nephrons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased methylmalonyl-coa mutase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased methylmalonyl-coa mutase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased corneal reflex Gene Set From HPO Gene-Disease Associations genes associated with the decreased corneal reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased achilles reflex Gene Set From HPO Gene-Disease Associations genes associated with the decreased achilles reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of cd8+ t cells Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of cd8+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum estradiol Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum estradiol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of small peripheral myelinated nerve fibers Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of small peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased circulating acth level Gene Set From HPO Gene-Disease Associations genes associated with the decreased circulating acth level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased liver function Gene Set From HPO Gene-Disease Associations genes associated with the decreased liver function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased lacrimation Gene Set From HPO Gene-Disease Associations genes associated with the decreased lacrimation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum progesterone Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum progesterone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased beta-galactosidase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased beta-galactosidase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement c9 Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement c9 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement c3 Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement c3 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased urinary urate Gene Set From HPO Gene-Disease Associations genes associated with the decreased urinary urate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of large peripheral myelinated nerve fibers Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of large peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased renal tubular phosphate excretion Gene Set From HPO Gene-Disease Associations genes associated with the decreased renal tubular phosphate excretion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of cytochrome c oxidase in muscle tissue Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of cytochrome c oxidase in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased mitochondrial complex iii activity in liver tissue Gene Set From HPO Gene-Disease Associations genes associated with the decreased mitochondrial complex iii activity in liver tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased electroretinogram (erg) amplitude Gene Set From HPO Gene-Disease Associations genes associated with the decreased electroretinogram (erg) amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased circulating renin level Gene Set From HPO Gene-Disease Associations genes associated with the decreased circulating renin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum leptin Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum leptin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased fumarate hydratase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased fumarate hydratase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased methylcobalamin Gene Set From HPO Gene-Disease Associations genes associated with the decreased methylcobalamin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum ceruloplasmin Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum ceruloplasmin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement factor b Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement factor b phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement factor h Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement factor h phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum complement factor i Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum complement factor i phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased urine output Gene Set From HPO Gene-Disease Associations genes associated with the decreased urine output phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased distal sensory nerve action potential Gene Set From HPO Gene-Disease Associations genes associated with the decreased distal sensory nerve action potential phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased corneal thickness Gene Set From HPO Gene-Disease Associations genes associated with the decreased corneal thickness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased body weight Gene Set From HPO Gene-Disease Associations genes associated with the decreased body weight phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased sensory nerve conduction velocity Gene Set From HPO Gene-Disease Associations genes associated with the decreased sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased fetal movement Gene Set From HPO Gene-Disease Associations genes associated with the decreased fetal movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased testicular size Gene Set From HPO Gene-Disease Associations genes associated with the decreased testicular size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased serum ferritin Gene Set From HPO Gene-Disease Associations genes associated with the decreased serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased cervical spine mobility Gene Set From HPO Gene-Disease Associations genes associated with the decreased cervical spine mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased finger mobility Gene Set From HPO Gene-Disease Associations genes associated with the decreased finger mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial respiratory chain Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial complex iii Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial complex iii phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of cd4+ t cells Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of cd4+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased movement range in interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the decreased movement range in interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased retinal pigmentation with dispersion Gene Set From HPO Gene-Disease Associations genes associated with the decreased retinal pigmentation with dispersion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial atp synthase complex Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial atp synthase complex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased purine levels Gene Set From HPO Gene-Disease Associations genes associated with the decreased purine levels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased plasma total carnitine Gene Set From HPO Gene-Disease Associations genes associated with the decreased plasma total carnitine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased/absent ankle reflexes Gene Set From HPO Gene-Disease Associations genes associated with the decreased/absent ankle reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased hip abduction Gene Set From HPO Gene-Disease Associations genes associated with the decreased hip abduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased central vision Gene Set From HPO Gene-Disease Associations genes associated with the decreased central vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of mitochondrial complex i Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of mitochondrial complex i phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased muscle glycogen content Gene Set From HPO Gene-Disease Associations genes associated with the decreased muscle glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased plasma carnitine Gene Set From HPO Gene-Disease Associations genes associated with the decreased plasma carnitine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased mean platelet volume Gene Set From HPO Gene-Disease Associations genes associated with the decreased mean platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased activity of the pyruvate dehydrogenase (pdh) complex Gene Set From HPO Gene-Disease Associations genes associated with the decreased activity of the pyruvate dehydrogenase (pdh) complex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased pyruvate carboxylase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased pyruvate carboxylase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thymic hormone decreased Gene Set From HPO Gene-Disease Associations genes associated with the thymic hormone decreased phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased testosterone in males Gene Set From HPO Gene-Disease Associations genes associated with the decreased testosterone in males phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of peripheral myelinated nerve fibers Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased plasma free carnitine Gene Set From HPO Gene-Disease Associations genes associated with the decreased plasma free carnitine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased patellar reflex Gene Set From HPO Gene-Disease Associations genes associated with the decreased patellar reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased pulmonary function Gene Set From HPO Gene-Disease Associations genes associated with the decreased pulmonary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased glomerular filtration rate Gene Set From HPO Gene-Disease Associations genes associated with the decreased glomerular filtration rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased taste sensation Gene Set From HPO Gene-Disease Associations genes associated with the decreased taste sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased beta-glucocerebrosidase protein and activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased beta-glucocerebrosidase protein and activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased motor nerve conduction velocity Gene Set From HPO Gene-Disease Associations genes associated with the decreased motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased amplitude of sensory action potentials Gene Set From HPO Gene-Disease Associations genes associated with the decreased amplitude of sensory action potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased miniature endplate potentials Gene Set From HPO Gene-Disease Associations genes associated with the decreased miniature endplate potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased subcutaneous fat Gene Set From HPO Gene-Disease Associations genes associated with the decreased subcutaneous fat phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased size of nerve terminals Gene Set From HPO Gene-Disease Associations genes associated with the decreased size of nerve terminals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased sensitivity to hypoxemia Gene Set From HPO Gene-Disease Associations genes associated with the decreased sensitivity to hypoxemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased sweating due to autonomic dysfunction Gene Set From HPO Gene-Disease Associations genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased platelet glycoprotein iib-iiia Gene Set From HPO Gene-Disease Associations genes associated with the decreased platelet glycoprotein iib-iiia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased methionine synthase activity Gene Set From HPO Gene-Disease Associations genes associated with the decreased methionine synthase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased adipose tissue Gene Set From HPO Gene-Disease Associations genes associated with the decreased adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased bone mineral density of femur Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased bone mineral density of femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased placental labyrinth size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased placental labyrinth size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine urea nitrogen level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased osteoclast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased osteoclast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased oocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased oocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to viral infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating thyroid-stimulating hormone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating thyroid-stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased erythrocyte potassium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased erythrocyte potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating triiodothyronine level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interferon-alpha level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interferon-alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased enteric neural crest cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased enteric neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased oviduct weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased oviduct weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased eosinophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased eosinophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver free fatty acids level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver free fatty acids level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trabecular bone connectivity density Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trabecular bone connectivity density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-17 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-17 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased compensatory feeding amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased compensatory feeding amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased percent body fat Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased percent body fat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mean corpuscular volume Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mean corpuscular volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-2 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-2 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mast cell degranulation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mast cell degranulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased glomerular capillary number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased glomerular capillary number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear hair cell stereocilia number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased number of peritubular myoid cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased number of peritubular myoid cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased embryonic neuroepithelium thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased embryonic neuroepithelium thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased igd level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased igd level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased transitional stage t2 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased transitional stage t2 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased small intestinal microvillus size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased small intestinal microvillus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased striatum area Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased striatum area phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trophoblast glycogen cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trophoblast glycogen cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nk cell degranulation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nk cell degranulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating aldosterone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal tubule apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal tubule apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-1 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-1 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neuronal stem cell self-renewal Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neuronal stem cell self-renewal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-12b secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-12b secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to neuronal excitotoxicity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased gonadal fat pad weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased gonadal fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating ghrelin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ghrelin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to bacterial infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased erythrocyte magnesium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased erythrocyte magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased keratinocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased keratinocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hepatocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hepatocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased blood urea nitrogen level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased blood urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating complement protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating complement protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased secondary ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased secondary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trabecular bone thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trabecular bone thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased saturated fatty acid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased saturated fatty acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trabecular bone volume Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trabecular bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased digestive secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased digestive secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased plasma cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver regeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased respiratory mucosa goblet cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased respiratory mucosa goblet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased systemic arterial blood pressure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vitamin d level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vitamin d level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induced joint inflammation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced joint inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pulmonary endothelial cell surface Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pulmonary endothelial cell surface phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased body length Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased body length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased number of pulmonary neuroendocrine bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreas weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreas weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cd8-positive, alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal glomerular filtration rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal glomerular filtration rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased aggression towards mice Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased aggression towards mice phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased oligodendrocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased oligodendrocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating magnesium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased a wave amplitude Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased a wave amplitude phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skeletal muscle fiber density Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skeletal muscle fiber density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating gastrin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating gastrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lymph node number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lymph node number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating ketone body level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ketone body level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased behavioral withdrawal response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased behavioral withdrawal response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased triiodothyronine level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fatty acid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fatty acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased length of long bones Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased length of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dopamine level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dopamine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased abdominal adipose tissue amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased abdominal adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating factor ix level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating factor ix level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased keratohyalin granule number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased keratohyalin granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating chloride level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating chloride level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased osteoid thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased osteoid thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skin turgor Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skin turgor phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-2 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-2 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t-helper 17 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t-helper 17 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased amacrine cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased amacrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prostate gland weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prostate gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased atrioventricular cushion size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased atrioventricular cushion size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased acute inflammation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased acute inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating gonadotropin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating gonadotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased creatine kinase level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased creatine kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased adrenal gland weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased adrenal gland weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine prostaglandin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine prostaglandin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tear production Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tear production phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased axial mesoderm size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased axial mesoderm size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spleen white pulp amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spleen white pulp amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hepatoblast number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hepatoblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mitochondrial dna content Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mitochondrial dna content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased chondrocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased chondrocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sterol level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating unsaturated transferrin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating unsaturated transferrin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating alanine transaminase level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating alanine transaminase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver copper level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver copper level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skeletal muscle weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skeletal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased long bone epiphyseal plate size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased long bone epiphyseal plate size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased corticospinal tract size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased corticospinal tract size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased bone mineral density Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased bone mineral density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased body mass index Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased body mass index phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pulmonary vascular resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pulmonary vascular resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased otic epithelium proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased otic epithelium proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased keratohyalin granule size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased keratohyalin granule size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine major urinary protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine major urinary protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased integument system tumor incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased integument system tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased intestinal cholesterol absorption Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased intestinal cholesterol absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vagina weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vagina weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased extensor digitorum longus weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased extensor digitorum longus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to kidney reperfusion injury Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to kidney reperfusion injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tumor latency Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tumor latency phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased epididymis weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased epididymis weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-5 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-5 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased activation-induced b cell apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased activation-induced b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cranium width Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cranium width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prostate gland duct number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prostate gland duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased ovulation rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased ovulation rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased bleeding time Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased bleeding time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lymphoma incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lymphoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sensitivity to induced cell death Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased subcutaneous adipose tissue amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased subcutaneous adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased incidence of tumors by chemical induction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased incidence of tumors by chemical induction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cell mass Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cell mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cns synapse formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cns synapse formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fluid intake Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fluid intake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased purine-nucleoside phosphorylase activity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased purine-nucleoside phosphorylase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating adrenaline level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating adrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nerve conduction velocity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nerve conduction velocity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tongue size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tongue size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased ige level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased ige level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to bone fracture Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to bone fracture phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased serotonin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased serotonin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine osmolality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine osmolality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased otolith number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased otolith number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lipoprotein lipase activity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lipoprotein lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased embryo size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased embryo size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased organ/body region tumor incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased organ/body region tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nk t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nk t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased ductal branching in the coagulating gland Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased ductal branching in the coagulating gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine flow rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine flow rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased double-negative t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased double-negative t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mast cell protease storage Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mast cell protease storage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased primordial ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased common myeloid progenitor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased common myeloid progenitor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased embryonic cilium length Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased embryonic cilium length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal cone cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cardiomyocyte apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cardiomyocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine glucose level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interscapular fat pad weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interscapular fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic endocrine progenitor cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic endocrine progenitor cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased luteinizing hormone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased luteinizing hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interferon-gamma secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interferon-gamma secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased incidence of tumors by ionizing radiation induction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased incidence of tumors by ionizing radiation induction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating atrial natriuretic factor Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating atrial natriuretic factor phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear nerve compound action potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear nerve compound action potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cytotoxic t cell cytolysis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cytotoxic t cell cytolysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induction of seizure by inducing agent Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induction of seizure by inducing agent phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-1 beta level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-1 beta level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased inner cell mass proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased inner cell mass proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear microphonics Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear microphonics phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lean body mass Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lean body mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased small intestinal villus size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased small intestinal villus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased diameter of femur Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased diameter of femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased adrenocorticotropin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased adrenocorticotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased corneal stroma thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased corneal stroma thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased colliculi size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased colliculi size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased brain size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased brain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lumbar vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lumbar vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased b-1b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased b-1b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hippocampal commissure size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hippocampal commissure size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased stereotypic behavior Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased stereotypic behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased germ cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased germ cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine phosphate level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine phosphate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic beta cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic beta cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cajal-retzius cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cajal-retzius cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased airway resistance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased airway resistance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic islet number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic islet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skin tensile strength Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skin tensile strength phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased aorta elastin content Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased aorta elastin content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased ovary weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased ovary weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t cell apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cerebellar granule cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cerebellar granule cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spongiotrophoblast size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spongiotrophoblast size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nerve fiber response threshold Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nerve fiber response threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased salivation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased salivation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating creatine kinase level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating creatine kinase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased energy expenditure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased energy expenditure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-6 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-6 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased survivor rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased survivor rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased platelet calcium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased platelet calcium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased core body temperature Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased core body temperature phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating progesterone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating progesterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vasoconstriction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vasoconstriction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tibialis anterior weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tibialis anterior weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased heart rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased heart rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to type ii hypersensitivity reaction Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to type ii hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased single-positive t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased single-positive t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating renin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating renin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased thymocyte apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased thymocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased rib number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased rib number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased diameter of long bones Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased diameter of long bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to parasitic infection Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-12 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-12 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased kidney collecting duct number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased kidney collecting duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased total retina thickness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased total retina thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased follicle stimulating hormone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased follicle stimulating hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cellular sensitivity to alkylating agents Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to alkylating agents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prepulse inhibition Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prepulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal cardiomyocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal cardiomyocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased paired-pulse facilitation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased paired-pulse facilitation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased platelet serotonin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased platelet serotonin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prostaglandin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prostaglandin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cardiac output Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cardiac output phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to experimental autoimmune myasthenia gravis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to experimental autoimmune myasthenia gravis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased kidney cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased kidney cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine aldosterone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-9 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-9 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lung endothelial cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lung endothelial cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating glucagon level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glucagon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sebaceous gland number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sebaceous gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating creatine level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating creatine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cardiac stroke volume Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cardiac stroke volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased clearance of atrial thrombosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased clearance of atrial thrombosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased igm level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased igm level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating glucocorticoid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glucocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased systemic arterial systolic blood pressure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased systemic arterial systolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating insulin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating insulin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased unsaturated fatty acid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased unsaturated fatty acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lateral semicircular canal size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lateral semicircular canal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased endocochlear potential Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased endocochlear potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased erythroblast number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased erythroblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interferon-gamma level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interferon-gamma level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver function Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spleen germinal center size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spleen germinal center size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-4 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-4 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to experimental autoimmune uveoretinitis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to experimental autoimmune uveoretinitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine potassium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating total protein level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating total protein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased myocardial fiber number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased myocardial fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating bilirubin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating bilirubin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased zigzag hair amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased zigzag hair amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cerebral infarction size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cerebral infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased threshold for auditory brainstem response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased threshold for auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-5 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-5 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased channel response intensity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased channel response intensity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased level of surface class i molecules Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased level of surface class i molecules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating prothrombin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating prothrombin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased synaptic depression Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased synaptic depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to bacterial infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased brown adipose tissue amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased brown adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating ceruloplasmin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ceruloplasmin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating mineralocorticoid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating mineralocorticoid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mitochondria number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mitochondria number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prolactin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prolactin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tubuloglomerular feedback response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tubuloglomerular feedback response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased blood uric acid level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased blood uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased left ventricle developed pressure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased left ventricle developed pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver glycogen level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver glycogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-13 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-13 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased response of heart to induced stress Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased response of heart to induced stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hematopoietic stem cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hematopoietic stem cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cellular sensitivity to ultraviolet irradiation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to ultraviolet irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased macrophage nitric oxide production Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased macrophage nitric oxide production phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-10 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-10 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t-helper 2 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t-helper 2 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic delta cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic delta cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased molar number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased molar number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine corticosterone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine corticosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased chemical nociceptive threshold Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased chemical nociceptive threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased heart left ventricle weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased heart left ventricle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating hdl cholesterol level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating hdl cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tumor growth/size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tumor growth/size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lactate dehydrogenase level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lactate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating testosterone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating testosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased defecation amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased defecation amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased glyceraldehyde-3-phosphate dehydrogenase (nad+) (phosphorylating) activity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased glyceraldehyde-3-phosphate dehydrogenase (nad+) (phosphorylating) activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased splenocyte proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased splenocyte proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pituitary hormone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pituitary hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased metatarsal bone number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased metatarsal bone number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased autoantibody level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased autoantibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to atherosclerosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to atherosclerosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dn1 thymic pro-t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dn1 thymic pro-t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pp cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pp cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased liver cholesterol level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased liver cholesterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased b-1a cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased b-1a cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to induced pancreatitis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced pancreatitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased glycogen catabolism rate Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased glycogen catabolism rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lung tumor incidence Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lung tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased endolymph production Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased endolymph production phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine creatinine level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine creatinine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased satellite cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased satellite cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating prolactin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating prolactin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased gamma-delta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased gamma-delta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cellular sensitivity to gamma-irradiation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cellular sensitivity to gamma-irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased inferior colliculus size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased inferior colliculus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hair follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hair follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating potassium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating potassium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mature b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mature b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-1 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-1 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine ammonia level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine ammonia level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreas regeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreas regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cranium length Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cranium length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased platelet atp level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased platelet atp level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating parathyroid hormone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating parathyroid hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interleukin-18 secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interleukin-18 secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased left ventricle diastolic pressure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased left ventricle diastolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating adrenocorticotropin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating adrenocorticotropin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased immature b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased immature b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hepatocyte apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hepatocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased heart left ventricle size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased heart left ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased macrophage cytokine production Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased macrophage cytokine production phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased splenocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased splenocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased placenta weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased placenta weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased macrophage cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased macrophage cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cumulus expansion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cumulus expansion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic acinar cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic acinar cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to osteoporosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to osteoporosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tendon stiffness Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tendon stiffness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine magnesium level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine magnesium level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased startle reflex Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased startle reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased grooming behavior Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased grooming behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to injury Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased transitional stage b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased transitional stage b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to weight loss Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased erythroid progenitor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased erythroid progenitor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sebocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sebocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating dihydrotestosterone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating dihydrotestosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased noradrenaline level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased noradrenaline level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased primordial germ cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased primordial germ cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased midbrain size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased midbrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased superior semicircular canal size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased superior semicircular canal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skeletal muscle fiber diameter Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skeletal muscle fiber diameter phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal photoreceptor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine albumin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine albumin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hematopoietic stem cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hematopoietic stem cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased kidney apoptosis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased kidney apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating bicarbonate level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating bicarbonate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dentate gyrus size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dentate gyrus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased caudal vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased caudal vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased total body fat amount Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased total body fat amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating glucose level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased paraxial mesoderm size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased paraxial mesoderm size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased igg2a level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased igg2a level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased memory b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased memory b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cell migration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased thyroxine level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased thyroxine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to infection induced morbidity/mortality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hepatocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hepatocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased physiological sensitivity to xenobiotic Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased physiological sensitivity to xenobiotic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased exploration in new environment Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased exploration in new environment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mammary gland epithelium proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mammary gland epithelium proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tympanic ring size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tympanic ring size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased myocardial infarction size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased myocardial infarction size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased superior colliculus size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased superior colliculus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased diastolic filling velocity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased diastolic filling velocity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine nitrite level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine nitrite level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased granulocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased granulocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased excitatory postsynaptic current amplitude Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased excitatory postsynaptic current amplitude phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased somatotroph secretory granule number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased somatotroph secretory granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased glucokinase activity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased glucokinase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased igg1 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased igg1 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t helper 1 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t helper 1 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating interleukin-18 level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating interleukin-18 level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vascular endothelial cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vascular endothelial cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased susceptibility to age related obesity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to age related obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trabecular bone mass Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trabecular bone mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased birth body size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased birth body size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased transitional stage t1 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased transitional stage t1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lung elastance Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lung elastance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased body weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased body weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased urine ph Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased urine ph phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lactotroph cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lactotroph cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lung weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lung weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased surfactant secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased surfactant secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased aerobic running capacity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased aerobic running capacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased anti-nuclear antigen antibody level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased anti-nuclear antigen antibody level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased omental fat pad weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased omental fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spleen iron level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spleen iron level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased uterine fat pad weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased uterine fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased rhombomere 6 size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased rhombomere 6 size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased submandibular gland size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased submandibular gland size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased total tissue mass Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased total tissue mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased monocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased monocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased left ventricle systolic pressure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased left ventricle systolic pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased posterior semicircular canal size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased posterior semicircular canal size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cellular hemoglobin content Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cellular hemoglobin content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating glycerol level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating glycerol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased interferon-beta secretion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased interferon-beta secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased activity of parathyroid Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased activity of parathyroid phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased visual acuity Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased muscle spindle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased muscle spindle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mitochondria size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mitochondria size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased soleus weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased soleus weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased collagen level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased collagen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lung endothelial cell migration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lung endothelial cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased inflammatory response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased inflammatory response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased primary ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased primary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased respiratory quotient Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased respiratory quotient phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased rhombomere 5 size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased rhombomere 5 size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating pituitary hormone level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating pituitary hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lymphatic vessel endothelial cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lymphatic vessel endothelial cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased corpora lutea number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased corpora lutea number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased aggression Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased aggression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased white fat cell size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased circulating ferritin level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased circulating ferritin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dopaminergic neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dopaminergic neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased heart weight Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased heart weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neurotransmitter release Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neurotransmitter release phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased coping response Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased coping response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased enteric neural crest cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased enteric neural crest cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hindbrain size Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hindbrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased brain sterol level Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased brain sterol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased regulatory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Harmonizome 3.0

decreased cranial base ossification Gene Set

Decreased Cranial Base Ossification Gene Set

base-excision repair, AP site formation via deaminated base removal Gene Set

base-excision repair, AP site formation via deaminated base removal Gene Set

ossification of posterior longitudinal ligament; ossification, heterotopic Gene Set

decreased cranial neural crest cell proliferation Gene Set

decreased cranial neural crest cell number Gene Set

decreased cranial neural crest cell proliferation Gene Set

decreased cranial neural crest cell number Gene Set

decreased calvarial ossification Gene Set

decreased skull ossification Gene Set

Decreased Calvarial Ossification Gene Set

decreased bone ossification Gene Set

proteasome regulatory particle, base subcomplex Gene Set

cytosolic trna wobble base thiouridylase complex Gene Set

Bandrowski's base Gene Set

skull base chordoma Gene Set

skull base meningioma Gene Set

skull base neoplasm Gene Set

base Gene Set

rrna base methylation Gene Set

trna wobble base modification Gene Set

base conversion or substitution editing Gene Set

base-excision repair, ap site formation Gene Set

base-excision repair, gap-filling Gene Set

base-excision repair, dna ligation Gene Set

base-excision repair Gene Set

proteasome regulatory particle, base subcomplex Gene Set

ciliary base Gene Set

pyrimidine-specific mismatch base pair dna n-glycosylase activity Gene Set

oxidized base lesion dna n-glycosylase activity Gene Set

mismatch base pair dna n-glycosylase activity Gene Set

deaminated base dna n-glycosylase activity Gene Set

site-specific endodeoxyribonuclease activity, specific for altered base Gene Set

purine-specific mismatch base pair dna n-glycosylase activity Gene Set

single base insertion or deletion binding Gene Set

sclerosis of skull base Gene Set

abnormality of the skull base Gene Set

abnormality of acid-base homeostasis Gene Set

sclerosis of skull base Gene Set

progressive sclerosis of skull base Gene Set

cleft in skull base Gene Set

abnormal nasal base Gene Set

pyramidal skinfold extending from the base to the top of the nails Gene Set

abnormality of the skull base Gene Set

wide nasal base Gene Set

thick skull base Gene Set

abnormality of acid-base homeostasis Gene Set

Skull Base Neoplasms Gene Set

Helix-turn-helix, base-excision DNA repair, C-terminal Gene Set

Schiff base-forming aldolase, active site Gene Set

abnormal base-excision repair Gene Set

Base-free sugar-phosphate removal via the single-nucleotide replacement pathway Gene Set

Base-Excision Repair, AP Site Formation Gene Set

Base Excision Repair Gene Set

leaf base Gene Set

shoot base Gene Set

Skull Base Chordoma Gene Set

Pyramidal Skinfold Extending From The Base To The Top Of The Nails Gene Set

Skull Base Meningioma Gene Set

Abnormality Of The Skull Base Gene Set

Carcinoma Of Base Of Tongue Gene Set

Wide Nasal Base Gene Set

Narrow Nasal Base Gene Set

Thick Skull Base Gene Set

Cleft In Skull Base Gene Set

Progressive Sclerosis Of Skull Base Gene Set

rRNA base methylation Gene Set

base-excision repair Gene Set

base-excision repair, gap-filling Gene Set

regulation of base-excision repair Gene Set

positive regulation of base-excision repair Gene Set

telomere maintenance via base-excision repair Gene Set

base-excision repair, AP site formation Gene Set

base-excision repair, DNA ligation Gene Set

base conversion or substitution editing Gene Set

tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation Gene Set

tRNA wobble base cytosine methylation Gene Set

tRNA wobble base modification Gene Set