Results for "Peters anomaly": 104 gene sets

Name

Peters anomaly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peters anomaly from the curated CTD Gene-Disease Associations dataset.

peters anomaly Gene Set

From HPO Gene-Disease Associations

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

peters anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the peters anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

Peters anomaly Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Peters anomaly from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Peters anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Peters anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

peters' anomaly Gene Set

From GAD Gene-Disease Associations

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

Peters plus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peters plus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

peters Gene Set

From GeneRIF Biological Term Annotations

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

peters-plus syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the peters-plus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Peters plus syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Peters plus syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Peters plus syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Peters plus syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Peters plus syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Peters plus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

May-Hegglin anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the May-Hegglin anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pelger-Huët anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pelger-Huët anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Axenfeld anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Axenfeld anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Axenfeld-rieger anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Axenfeld-rieger anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Caudal Duplication Anomaly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Caudal Duplication Anomaly from the curated CTD Gene-Disease Associations dataset.

Pelger-Huet Anomaly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pelger-Huet Anomaly from the curated CTD Gene-Disease Associations dataset.

coronary artery anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

pelger-huet anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

ebstein anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

anomaly Gene Set

From GeneRIF Biological Term Annotations

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

anomaly of the upper limb diaphyses Gene Set

From GWASdb SNP-Phenotype Associations

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

anomaly of the limb diaphyses Gene Set

From GWASdb SNP-Phenotype Associations

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

branchial anomaly Gene Set

From HPO Gene-Disease Associations

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

vertebral arch anomaly Gene Set

From HPO Gene-Disease Associations

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

malar anomaly Gene Set

From HPO Gene-Disease Associations

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

axenfeld anomaly Gene Set

From HPO Gene-Disease Associations

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

eye of the tiger anomaly of globus pallidus Gene Set

From HPO Gene-Disease Associations

genes associated with the eye of the tiger anomaly of globus pallidus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

urogenital sinus anomaly Gene Set

From HPO Gene-Disease Associations

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

sprengel anomaly Gene Set

From HPO Gene-Disease Associations

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

anorectal anomaly Gene Set

From HPO Gene-Disease Associations

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

rieger anomaly Gene Set

From HPO Gene-Disease Associations

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

sperm head anomaly Gene Set

From HPO Gene-Disease Associations

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

duane anomaly Gene Set

From HPO Gene-Disease Associations

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

anomaly of the limb diaphyses Gene Set

From HPO Gene-Disease Associations

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

Ebstein Anomaly Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ebstein Anomaly phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

?caudal duplication anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?caudal duplication anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

conotruncal anomaly face syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the conotruncal anomaly face syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

pelger-huet anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

may-hegglin anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the may-hegglin anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

?morning glory disc anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?morning glory disc anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

scaphocephaly and axenfeld-rieger anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the scaphocephaly and axenfeld-rieger anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

Ebstein Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ebstein Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Pelger-Huet Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Pelger-Huet Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Conotruncal Anomaly Face Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Conotruncal Anomaly Face Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Caudal Duplication Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Caudal Duplication Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Anomaly Of Anterior Segment Of Eye Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Anomaly Of Anterior Segment Of Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Taussig-Bing Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Taussig-Bing Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Anomaly Of Aortic Arch Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Anomaly Of Aortic Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Urogenital Sinus Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Urogenital Sinus Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Pulmonary Venous Return Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Pulmonary Venous Return Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Vitreous Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Vitreous Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Axenfeld Anomaly (Disorder) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Axenfeld Anomaly (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Brain Small Vessel Disease With Axenfeld-Rieger Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Brain Small Vessel Disease With Axenfeld-Rieger Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Anomaly Of Rectum Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Anomaly Of Rectum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Gallbladder Anomaly Congenital Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Gallbladder Anomaly Congenital in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Morning Glory Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Morning Glory Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Presentey Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Presentey Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Acquired Anomaly Of Tongue Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Acquired Anomaly Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Anomaly Of Tongue Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Anomaly Of Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Uhl Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Uhl Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Neurodevelopmental Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Neurodevelopmental Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Axenfeld-Rieger Anomaly With Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, And Skeletal Abnormalities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Anomaly Of Eyelid Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Anomaly Of Eyelid in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Anomaly Of Nose Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Anomaly Of Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Optic Disc Structural Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Optic Disc Structural Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Ebstein'S Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Ebstein'S Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Major Congenital Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Major Congenital Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Anomaly Of Ischium Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Anomaly Of Ischium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Branchial Anomaly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Branchial Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

May-Hegglin Anomaly Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype May-Hegglin Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Vascular Anomaly Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Vascular Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Vertebral Arch Anomaly Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Vertebral Arch Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Sperm Tail Anomaly Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Sperm Tail Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Eye Of The Tiger Anomaly Of Globus Pallidus Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Eye Of The Tiger Anomaly Of Globus Pallidus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Anomaly Of Placenta Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Anomaly Of Placenta in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Sperm Head Anomaly Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Sperm Head Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Pseudo Pelger-Huet Anomaly Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Pseudo Pelger-Huet Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Klippel-Feil Anomaly Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Klippel-Feil Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Sperm Mid-Piece Anomaly Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Sperm Mid-Piece Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Coronary artery anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Coronary artery anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Pelger-Huet anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Pelger-Huet anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Central conducting lymphatic anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Central conducting lymphatic anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Ebstein anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Ebstein anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Generalized lymphatic anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Generalized lymphatic anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia due to collagen 9 anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia due to collagen 9 anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Congenital anomaly of kidney and urinary tract Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital anomaly of kidney and urinary tract phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Scaphocephaly and axenfeld-rieger anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Scaphocephaly and axenfeld-rieger anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Short stature due to growth hormone qualitative anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Short stature due to growth hormone qualitative anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

T-substance anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the T-substance anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Short stature-optic atrophy-Pelger-Huet anomaly syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Short stature-optic atrophy-Pelger-Huet anomaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Ebstein anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Ebstein anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Congenital total pulmonary venous return anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital total pulmonary venous return anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Branchial cleft anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Branchial cleft anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Pelger-Huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Pelger-Huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Rieger anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Rieger anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Arthrogryposis-like hand anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Arthrogryposis-like hand anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Familial cavitary optic disk anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Familial cavitary optic disk anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Congenital anomaly of face Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital anomaly of face phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Axenfeld-Rieger anomaly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Axenfeld-Rieger anomaly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.