Caudal Duplication Anomaly

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Results for "Caudal Duplication Anomaly": 433 gene sets

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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.
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.
?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.
rostral-caudal axis duplication Gene Set From MPO Gene-Phenotype Associations gene mutations causing the rostral-caudal axis duplication phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
rostral-caudal axis duplication Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the rostral-caudal axis duplication phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Caudal duplication Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Caudal duplication 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.
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.
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.
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.
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.
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.
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.
peters anomaly Gene Set From OMIM Gene-Disease Associations genes associated with the peters 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.
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.
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.
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.
Williams-Beuren Region Duplication Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Williams-Beuren Region Duplication Syndrome from the curated CTD Gene-Disease Associations dataset.
duplication Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term duplication in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
centrosome duplication Gene Set From GO Biological Process Annotations 2015 genes participating in the centrosome duplication biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2015 dataset.
duplication of phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fibular duplication Gene Set From HPO Gene-Disease Associations genes associated with the fibular duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of distal phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the duplication of distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the phalanges of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of thumb phalanx Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal duplication Gene Set From HPO Gene-Disease Associations genes associated with the renal duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of bones involving the upper extremities Gene Set From HPO Gene-Disease Associations genes associated with the duplication of bones involving the upper extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ureteral duplication Gene Set From HPO Gene-Disease Associations genes associated with the ureteral duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the phalanges of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the phalanges of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the phalanges of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of renal pelvis Gene Set From HPO Gene-Disease Associations genes associated with the duplication of renal pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of middle phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the duplication of middle phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of phalanx of 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of hand bones Gene Set From HPO Gene-Disease Associations genes associated with the duplication of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of phalanx of 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of thumb phalanx Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of internal organs Gene Set From HPO Gene-Disease Associations genes associated with the duplication of internal organs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb duplication Gene Set From HPO Gene-Disease Associations genes associated with the limb duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of thumb phalanx Gene Set From HPO Gene-Disease Associations genes associated with the duplication of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the middle phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the middle phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the proximal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal urethral duplication Gene Set From HPO Gene-Disease Associations genes associated with the distal urethral duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of phalanx of hallux Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication involving bones of the feet Gene Set From HPO Gene-Disease Associations genes associated with the duplication involving bones of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Chromosome Duplication Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Duplication phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Friend of PRMT1 duplication Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Friend of PRMT1 duplication protein domain from the InterPro Predicted Protein Domain Annotations dataset.
chromosome 17q21.31 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q21.31 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xp11.23-p11.22 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xp11.23-p11.22 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
leri pleonosteosis chromosome duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the leri pleonosteosis chromosome duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 7q11.23 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 7q11.23 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
omphalocele due to duplication of 1p31.3 Gene Set From OMIM Gene-Disease Associations genes associated with the omphalocele due to duplication of 1p31.3 phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 1q21.1 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 1q21.1 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xq28 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xq28 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17q23.1-q23.2 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q23.1-q23.2 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 22q13 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 22q13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16p11.2 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16p11.2 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16p13.3 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16p13.3 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xq27.3-q28 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xq27.3-q28 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17p13.3 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17p13.3 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 2q31.1 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 2q31.1 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
split-hand/foot malformation 3, gene duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation 3, gene duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17q12 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q12 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 19p13.13 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 19p13.13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 5p13 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 5p13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Duplication Of Thumb Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duplication Of Thumb Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome Xq26.3 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Xq26.3 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 11Q Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 11Q Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Duplication Of Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Duplication Of Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Duplication Of Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Duplication Of Thumb Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of Thumb Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Duplication Of Proximal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of Proximal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Duplication Of Intestine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Duplication Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Duplication Of The Distal Phalanx Of The 2Nd Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Duplication Of The Distal Phalanx Of The 3Rd Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome Xq27.3-Q28 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Xq27.3-Q28 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Urethral Duplication Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Urethral Duplication in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome Xp11.23-P11.22 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Xp11.23-P11.22 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Duplication Of The Distal Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 5P13 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 5P13 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duplication Of Internal Organs Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duplication Of Internal Organs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17P13.3 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17P13.3 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duplication Of The Proximal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duplication Of The Proximal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Xq25 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Xq25 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17Q23.1-Q23.2 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17Q23.1-Q23.2 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duplication 15Q11-Q13 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duplication 15Q11-Q13 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Duplication Of Thumb Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Duplication Of Thumb Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Duplication Of The Distal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Duplication Of The Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Complete Duplication Of The Middle Phalanx Of The 3Rd Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Duplication Of The Middle Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Duplication Of Phalanx Of Hallux Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duplication Of Phalanx Of Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Duplication Of The Distal Phalanx Of Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duplication Of The Distal Phalanx Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Duplication Of Renal Pelvis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duplication Of Renal Pelvis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fibular Duplication Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibular Duplication in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosome Xq28 Duplication Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosome Xq28 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Complete Duplication Of Hallux Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Duplication Of Hallux Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2023 dataset.
duplication of ductus venosus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the duplication of ductus venosus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2025 dataset.
Chromosomal duplication syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosomal duplication syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
7q11.23 duplication syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease 7q11.23 duplication syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosomal duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosomal duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17p13.3 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17p13.3 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
7q11.23 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease 7q11.23 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome Xp11.22 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome Xp11.22 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 16p11.2 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 16p11.2 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 1q21.1 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 1q21.1 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17q21.31 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17q21.31 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gene duplication disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gene duplication disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17q12 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17q12 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 16p13.3 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 16p13.3 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 22q13 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 22q13 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system tumor with BCOR internal tandem duplication Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system tumor with BCOR internal tandem duplication in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 5p13 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 5p13 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intestinal duplication Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intestinal duplication phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
caudal group of intralaminar nuclei, right Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal group of intralaminar nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
caudal group of intralaminar nuclei, left Gene Set From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal group of intralaminar nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
mesomere 2 (preisthmus or caudal midbrain) Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in mesomere 2 (preisthmus or caudal midbrain) relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Lateral septal nucleus, caudal (caudodorsal) part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Lateral septal nucleus, caudal (caudodorsal) part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
subbrachial nucleus, caudal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in subbrachial nucleus, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r10 part of spinal trigeminal nucleus, caudal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r10 part of spinal trigeminal nucleus, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
caudal linear (raphe) nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in caudal linear (raphe) nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
caudal secondary prosencephalon Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in caudal secondary prosencephalon relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
r11 part of spinal trigeminal nucleus, caudal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in r11 part of spinal trigeminal nucleus, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Pallidum, caudal region Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pallidum, caudal region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
peduncular (caudal) hypothalamus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in peduncular (caudal) hypothalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
caudal zona incerta Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in caudal zona incerta relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal nucleus of the trigeminal, caudal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal nucleus of the trigeminal, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Spinal nucleus of the trigeminal, oral part, caudal dorsomedial part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Spinal nucleus of the trigeminal, oral part, caudal dorsomedial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
nucleus of the inferior collicular brachium, caudal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in nucleus of the inferior collicular brachium, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
caudal interpeduncular nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in caudal interpeduncular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Pontine reticular nucleus, caudal part Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Pontine reticular nucleus, caudal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
caudal ganglionic eminence_9 pcw_M_12833 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in caudal ganglionic eminence_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
caudal ganglionic eminence_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in caudal ganglionic eminence_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_25 pcw_F_12948 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_25 pcw_F_12948 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_21 pcw_F_12365 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12888 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
caudal ganglionic eminence_9 pcw_M_12833 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in caudal ganglionic eminence_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_37 pcw_M_263195015 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_11 yrs_F_12289 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
caudal ganglionic eminence_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in caudal ganglionic eminence_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12890 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_19 yrs_F_12832 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12889 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_4 mos_M_12889 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12981 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
posterior (caudal) superior temporal cortex (area 22c)_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in posterior (caudal) superior temporal cortex (area 22c)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
layer II of caudal entorhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in layer II of caudal entorhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in caudal midinferior temporal cortex (area TF) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in caudal subicular cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in caudal subicular cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SZ in caudal cingulate cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SZ in caudal cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
IZ in caudal midinferior temporal cortex (area TF) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
layer IIIa of caudal entorhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in layer IIIa of caudal entorhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
pyramidal layer of caudal subiculum Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in pyramidal layer of caudal subiculum relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
lower (caudal) rhombic lip Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in lower (caudal) rhombic lip relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
deep layers of caudal entorhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in deep layers of caudal entorhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
caudal portion of VFC (area 44) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal portion of VFC (area 44) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
MZ in caudal cingulate cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in caudal cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
caudal presubiculum (postsubiculum) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal presubiculum (postsubiculum) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
caudal prosubiculum Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal prosubiculum relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
layer IIIb of caudal entorhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in layer IIIb of caudal entorhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
granular layer of caudal dentate gyrus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in granular layer of caudal dentate gyrus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
stratum oriens of caudal CA1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in stratum oriens of caudal CA1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner CP in caudal cingulate cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in caudal cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
IZ in caudal perirhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in caudal perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
caudal (posterior) extramural migratory stream Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal (posterior) extramural migratory stream relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
pyramidal cells of caudal CA4 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in pyramidal cells of caudal CA4 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
layer I of caudal entorhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in layer I of caudal entorhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
caudal subdivision of paraventricular nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal subdivision of paraventricular nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner CP in caudal midinferior temporal cortex (area TF) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner CP in caudal perirhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in caudal perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
caudal putamen Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal putamen relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in caudal midinferior temporal cortex (area TF) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
IZ in caudal cingulate cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in caudal cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
inner SZ in caudal midinferior temporal cortex (area TF) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer SZ in caudal midinferior temporal cortex (area TF) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
MZ in caudal perirhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in caudal perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SG in caudal entorhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in caudal entorhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer CP in caudal midinferior temporal cortex (area TF) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in caudal midinferior temporal cortex (area TF) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
superficial layers of caudal presubiculum Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in superficial layers of caudal presubiculum relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
CP in caudal subicular cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in CP in caudal subicular cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
caudal division of IPC (area 39) Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal division of IPC (area 39) relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in caudal hippocampal proper Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in caudal hippocampal proper relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
polymorphic layer of caudal subiculum Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in polymorphic layer of caudal subiculum relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
layer III of caudal entorhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in layer III of caudal entorhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in caudal perirhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in caudal perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SG in caudal perirhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in caudal perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
layer VI of caudal entorhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in layer VI of caudal entorhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
stratum lacunosum-moleculare of caudal CA1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in stratum lacunosum-moleculare of caudal CA1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
layer V of caudal entorhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in layer V of caudal entorhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in caudal cingulate cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in caudal cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
stratum pyramidale of caudal CA1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in stratum pyramidale of caudal CA1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
stratum pyramidale of caudal CA3 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in stratum pyramidale of caudal CA3 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
stratum pyramidale of caudal CA2 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in stratum pyramidale of caudal CA2 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer CP in caudal cingulate cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in caudal cingulate cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
caudal ganglionic eminence Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal ganglionic eminence relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
caudal subdivision of medial nucleus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in caudal subdivision of medial nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
outer CP in caudal perirhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in caudal perirhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
subgranular zone of caudal dentate gyrus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in subgranular zone of caudal dentate gyrus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
CP in caudal hippocampus Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in CP in caudal hippocampus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
stratum radiatum of caudal CA1 Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in stratum radiatum of caudal CA1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in caudal hippocampal proper Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in caudal hippocampal proper relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
SP in caudal subicular cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in caudal subicular cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in caudal entorhinal cortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in caudal entorhinal cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
molecular layer of caudal subiculum Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in molecular layer of caudal subiculum relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
VZ in caudal cingulate neocortex Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in caudal cingulate neocortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Caudal regression syndrome Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Caudal regression syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
caudal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term caudal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
somite rostral/caudal axis specification Gene Set From GO Biological Process Annotations 2015 genes participating in the somite rostral/caudal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset.
caudal appendage Gene Set From HPO Gene-Disease Associations genes associated with the caudal appendage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
caudal interpedicular narrowing Gene Set From HPO Gene-Disease Associations genes associated with the caudal interpedicular narrowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Caudal-like activation domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Caudal-like activation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
incomplete caudal neuropore closure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the incomplete caudal neuropore closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
caudal vertebral transformation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the caudal vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal rostral-caudal axis patterning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal rostral-caudal axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
caudal body truncation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the caudal body truncation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal rostral-caudal body axis extension Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal rostral-caudal body axis extension phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal caudal vertebrae morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal caudal vertebrae morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
small caudal vertebrae Gene Set From MPO Gene-Phenotype Associations gene mutations causing the small caudal vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal rostral-caudal patterning of the somites Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal rostral-caudal patterning of the somites phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delayed caudal neuropore closure Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delayed caudal neuropore closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal right lung caudal lobe morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal right lung caudal lobe morphology 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.
short rostral-caudal axis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the short rostral-caudal axis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased caudal vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased caudal vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal caudal neuropore morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal caudal neuropore morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent caudal vertebrae Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent caudal vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
caudal rachischisis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the caudal rachischisis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
caudal vertebral fusion Gene Set From MPO Gene-Phenotype Associations gene mutations causing the caudal vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
caudal regression syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the caudal regression syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Caudal Regression Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Caudal Regression Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Caudal Dysplasia Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Caudal Dysplasia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Caudal Appendage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caudal Appendage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Caudal Interpedicular Narrowing Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caudal Interpedicular Narrowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Caudal Dysgenesis Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Caudal Dysgenesis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
somite rostral/caudal axis specification Gene Set From GO Biological Process Annotations 2023 genes participating in the somite rostral/caudal axis specification biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal rostral-caudal axis patterning Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal rostral-caudal axis patterning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
short rostral-caudal axis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the short rostral-caudal axis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
caudal body truncation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the caudal body truncation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
incomplete caudal neuropore closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the incomplete caudal neuropore closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased caudal vertebrae number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased caudal vertebrae number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal rostral-caudal patterning of the somites Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal rostral-caudal patterning of the somites phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
caudal vertebral fusion Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the caudal vertebral fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal rostral-caudal body axis extension Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal rostral-caudal body axis extension phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
caudal vertebral transformation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the caudal vertebral transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
small caudal vertebrae Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the small caudal vertebrae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal caudal vertebrae morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal caudal vertebrae morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased bone mineral density of caudal vertebrae Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased bone mineral density of caudal vertebrae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
caudal rachischisis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the caudal rachischisis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent caudal vertebrae Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent caudal vertebrae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased bone mineral density of caudal vertebrae Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased bone mineral density of caudal vertebrae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal right lung caudal lobe morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal right lung caudal lobe morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delayed caudal neuropore closure Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed caudal neuropore closure phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal caudal neuropore morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal caudal neuropore morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased caudal vertebrae number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased caudal vertebrae number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
caudal hemivertebra Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the caudal hemivertebra phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal caudal vertebrae morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal caudal vertebrae morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Caudal forebrain cell_Caudal forebrain_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Caudal forebrain cell_Caudal forebrain_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Caudal ganglionic eminence cell_Caudal ganglionic eminence_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Caudal ganglionic eminence cell_Caudal ganglionic eminence_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Caudal cortex cell_Caudal cortex_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Caudal cortex cell_Caudal cortex_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
somite rostral/caudal axis specification Gene Set From GO Biological Process Annotations 2025 genes participating in the somite rostral/caudal axis specification biological process from the curated GO Biological Process Annotations 2025 dataset.
Caudal regression syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Caudal regression syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Left caudal flagellum Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Left caudal flagellum cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Right caudal flagellum Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Right caudal flagellum cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Caudal regression sequence Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Caudal regression sequence phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Caudal anterior-cingulate cortex volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Caudal anterior-cingulate cortex volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Caudal middle frontal gyrus volume Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Caudal middle frontal gyrus volume phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

Caudal Duplication Anomaly Gene Set

Caudal Duplication Anomaly Gene Set

?caudal duplication anomaly Gene Set

rostral-caudal axis duplication Gene Set

rostral-caudal axis duplication Gene Set

Caudal duplication Gene Set

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

May-Hegglin anomaly Gene Set

Pelger-Huët anomaly Gene Set

Axenfeld anomaly Gene Set

Axenfeld-rieger anomaly Gene Set

Peters anomaly Gene Set

Pelger-Huet Anomaly Gene Set

coronary artery anomaly Gene Set

pelger-huet anomaly Gene Set

ebstein anomaly Gene Set

peters' anomaly Gene Set

anomaly Gene Set

anomaly of the upper limb diaphyses Gene Set

anomaly of the limb diaphyses Gene Set

branchial anomaly Gene Set

peters anomaly Gene Set

vertebral arch anomaly Gene Set

malar anomaly Gene Set

axenfeld anomaly Gene Set

eye of the tiger anomaly of globus pallidus Gene Set

urogenital sinus anomaly Gene Set

sprengel anomaly Gene Set

anorectal anomaly Gene Set

rieger anomaly Gene Set

sperm head anomaly Gene Set

duane anomaly Gene Set

anomaly of the limb diaphyses Gene Set

Ebstein Anomaly Gene Set

peters anomaly Gene Set

conotruncal anomaly face syndrome Gene Set

pelger-huet anomaly Gene Set

may-hegglin anomaly Gene Set

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

?morning glory disc anomaly Gene Set

scaphocephaly and axenfeld-rieger anomaly Gene Set

Ebstein Anomaly Gene Set

Pelger-Huet Anomaly Gene Set

Conotruncal Anomaly Face Syndrome Gene Set

Congenital Anomaly Of Anterior Segment Of Eye Gene Set

Taussig-Bing Anomaly Gene Set

Congenital Anomaly Of Aortic Arch Gene Set

Urogenital Sinus Anomaly Gene Set

Pulmonary Venous Return Anomaly Gene Set

Congenital Vitreous Anomaly Gene Set

Axenfeld Anomaly (Disorder) Gene Set

Brain Small Vessel Disease With Axenfeld-Rieger Anomaly Gene Set

Congenital Anomaly Of Rectum Gene Set

Gallbladder Anomaly Congenital Gene Set

Morning Glory Anomaly Gene Set

Presentey Anomaly Gene Set

Acquired Anomaly Of Tongue Gene Set

Congenital Anomaly Of Tongue Gene Set

Uhl Anomaly Gene Set

Neurodevelopmental Anomaly Gene Set

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

Congenital Anomaly Of Eyelid Gene Set

Congenital Anomaly Of Nose Gene Set

Optic Disc Structural Anomaly Gene Set

Familial Ebstein'S Anomaly Gene Set

Major Congenital Anomaly Gene Set

Congenital Anomaly Of Ischium Gene Set

Branchial Anomaly Gene Set

May-Hegglin Anomaly Gene Set

Vascular Anomaly Gene Set

Vertebral Arch Anomaly Gene Set

Sperm Tail Anomaly Gene Set

Eye Of The Tiger Anomaly Of Globus Pallidus Gene Set

Anomaly Of Placenta Gene Set

Sperm Head Anomaly Gene Set

Pseudo Pelger-Huet Anomaly Gene Set

Klippel-Feil Anomaly Gene Set

Sperm Mid-Piece Anomaly Gene Set

Peters anomaly Gene Set