Name

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 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 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 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.

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.

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 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.

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.

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.

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.

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 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 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.

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 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.

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 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.

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.

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.

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.

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.

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.

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 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.

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.

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.

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.

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.

aplasia of the middle phalanx of the hand Gene Set

From HPO Gene-Disease Associations

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

deviation of the hand or of fingers of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

radial deviation of the hand or of fingers of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the radial deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ulnar deviation of the hand or of fingers of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the ulnar deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Deviation Of The Hand Or Of Fingers Of The Hand Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Deviation Of The Hand Or Of Fingers Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Hand osteoarthritis severity (hand Klsum) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Hand osteoarthritis severity (hand Klsum) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Caudal Duplication Anomaly Gene Set

From CTD Gene-Disease Associations

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

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.

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.

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.

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.

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.

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.

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.

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 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.

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.

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.

?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.

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.

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.

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.

Caudal Duplication Anomaly Gene Set

From DisGeNET Gene-Disease Associations

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

Congenital 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.

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.

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.

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.

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.

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.

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.

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.

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 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.

abnormality of phalanx of finger Gene Set

From GWASdb SNP-Phenotype Associations

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

sclerosis of finger phalanx Gene Set

From GWASdb SNP-Phenotype Associations

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

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

From HPO Gene-Disease Associations

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

broad phalanx of the toes Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

symphalangism of middle phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

bracket epiphysis of the middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the bracket epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

enlarged epiphysis of the proximal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

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

absent middle phalanx of 5th finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of thumb phalanx Gene Set

From HPO Gene-Disease Associations

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

patchy sclerosis of finger phalanx Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

broad distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

slender proximal phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

triangular epiphysis of the middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

radial deviation of thumb terminal phalanx Gene Set

From HPO Gene-Disease Associations

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

triangular shaped proximal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

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

triangular shaped middle phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

sclerosis of distal finger phalanx Gene Set

From HPO Gene-Disease Associations

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

symphalangism of middle phalanx of 5th finger Gene Set

From HPO Gene-Disease Associations

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

long proximal phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

broad hallux phalanx Gene Set

From HPO Gene-Disease Associations

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

broad middle phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

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

short middle phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

hypersegmentation of proximal phalanx of second finger Gene Set

From HPO Gene-Disease Associations

genes associated with the hypersegmentation of proximal phalanx of second finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

slender distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

broad distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of the distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

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

bifid distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

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

short phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent proximal phalanx of thumb Gene Set

From HPO Gene-Disease Associations

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

short middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

short proximal phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the proximal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

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

triangular shaped middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the proximal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

broad distal phalanx of the toes Gene Set

From HPO Gene-Disease Associations

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

triangular epiphysis of the proximal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

broad distal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

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

triangular epiphysis of the proximal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

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

bracket epiphysis of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

abnormality of the proximal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

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

enlarged epiphysis of the middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the enlarged epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

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

From HPO Gene-Disease Associations

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

abnormality of the distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

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

short proximal phalanx of thumb Gene Set

From HPO Gene-Disease Associations

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

short middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fifth finger distal phalanx clinodactyly Gene Set

From HPO Gene-Disease Associations

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

abnormality of the distal phalanx of the hallux Gene Set

From HPO Gene-Disease Associations

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

abnormality of the proximal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

short proximal phalanx of hallux Gene Set

From HPO Gene-Disease Associations

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

abnormality of the distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

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

long distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

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

short phalanx of hallux Gene Set

From HPO Gene-Disease Associations

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

bifid distal phalanx of toe Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of toe Gene Set

From HPO Gene-Disease Associations

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

symphalangism affecting the proximal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphysis of the middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped proximal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular shaped proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypersegmentation of proximal phalanx of third finger Gene Set

From HPO Gene-Disease Associations

genes associated with the hypersegmentation of proximal phalanx of third finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

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

enlarged epiphysis of the proximal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the enlarged epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the proximal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sclerosis of finger phalanx Gene Set

From HPO Gene-Disease Associations

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

abnormality of the distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphysis of the proximal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

broad phalanx Gene Set

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

short middle phalanx of toe Gene Set

From HPO Gene-Disease Associations

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

abnormality of the distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the proximal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

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

abnormal phalanx morphology Gene Set

From MPO Gene-Phenotype Associations

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

Broad Hallux Phalanx Gene Set

From DisGeNET Gene-Disease Associations

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

Triangular Shaped Middle Phalanx Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Triangular Shaped Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Short Distal Phalanx Gene Set

From DisGeNET Gene-Disease Associations

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

Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Fifth Finger Distal Phalanx Clinodactyly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Fifth Finger Distal Phalanx Clinodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Broad Middle Phalanx Of Finger Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Broad Middle Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Radial Deviation Of Thumb Terminal Phalanx Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Radial Deviation Of Thumb Terminal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Triangular Shaped Distal Phalanx Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Triangular Shaped Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bifid Distal Phalanx Of Toe Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bifid Distal Phalanx Of Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Short Middle Phalanx Gene Set

From DisGeNET Gene-Disease Associations

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

Long Phalanx Of Finger Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Long Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hypersegmentation Of Proximal Phalanx Of Second Finger Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hypersegmentation Of Proximal Phalanx Of Second Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hypersegmentation Of Proximal Phalanx Of Third Finger Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hypersegmentation Of Proximal Phalanx Of Third Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Triangular Epiphysis Of The Middle Phalanx Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Triangular Epiphysis Of The Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Triangular Epiphysis Of The Proximal Phalanx Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Triangular Epiphysis Of The Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Triangular Shaped Proximal Phalanx Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Triangular Shaped Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Broad Distal Phalanx Of The Hallux Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Broad Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Long Distal Phalanx Of Finger Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Long Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Long Proximal Phalanx Of Finger Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Long Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Slender Proximal Phalanx Of Finger Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Slender Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bullet-Shaped Distal Phalanx Of The Hallux Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bullet-Shaped Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Short Distal Phalanx Gene Set

From DisGeNET Gene-Phenotype Associations

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

Short Phalanx Of Finger Gene Set

From DisGeNET Gene-Phenotype Associations

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

Broad Distal Phalanx Of Finger Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Broad Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Broad Phalanx Of The Toes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Broad Phalanx Of The Toes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Curved Toe Phalanx Gene Set

From DisGeNET Gene-Phenotype Associations

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

Broad Phalanx Gene Set

From DisGeNET Gene-Phenotype Associations

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

Short Middle Phalanx Gene Set

From DisGeNET Gene-Phenotype Associations

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

Short Proximal Phalanx Gene Set

From DisGeNET Gene-Phenotype Associations

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

Bifid Distal Phalanx Of The Thumb Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Bifid Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormality Of The Distal Phalanx Of The Thumb Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormality Of The Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Absent Proximal Phalanx Of Thumb Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Absent Proximal Phalanx Of Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Broad Distal Phalanx Of The Thumb Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Broad Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Absent Middle Phalanx Of 5Th Finger Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Absent Middle Phalanx Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Patchy Sclerosis Of Finger Phalanx Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Patchy Sclerosis Of Finger Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormality Of The Middle Phalanx Of The 5Th Finger Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormality Of The Middle Phalanx Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Slender Distal Phalanx Of Finger Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Slender Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormality Of The Proximal Phalanx Of The Thumb Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormality Of The Proximal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Broad Proximal Phalanx Of The Hallux Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Broad Proximal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Curved 4Th Toe Phalanx Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Curved 4Th Toe Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

abnormal phalanx morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal phalanx morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Symphalangism affecting the proximal phalanx of the 4th finger Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Symphalangism affecting the proximal phalanx of the 4th finger phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Triangular shaped proximal phalanx of the thumb Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Triangular shaped proximal phalanx of the thumb phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Split-hand/foot malformation 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hand foot uterus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hand foot uterus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaepiphyseal dysplasia short limb-hand type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaepiphyseal dysplasia short limb-hand type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split hand foot deformity 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split hand foot deformity 1 from the curated CTD Gene-Disease Associations dataset.

Heart-hand syndrome, Slovenian type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart-hand syndrome, Slovenian type from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation 6 from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation With Long Bone Deficiency 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 2 from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation With Long Bone Deficiency 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation With Long Bone Deficiency 3 from the curated CTD Gene-Disease Associations dataset.

Craniofacial deafness hand syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniofacial deafness hand syndrome from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation 4 from the curated CTD Gene-Disease Associations dataset.

Split-Hand/Foot Malformation 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-Hand/Foot Malformation 5 from the curated CTD Gene-Disease Associations dataset.

Hand Dermatoses Gene Set

From CTD Gene-Disease Associations

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

SPLIT-HAND/FOOT MALFORMATION 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPLIT-HAND/FOOT MALFORMATION 2 from the curated CTD Gene-Disease Associations dataset.

Hand Deformities, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hand Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.

Hand foot uterus syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hand foot uterus syndrome from the curated CTD Gene-Disease Associations dataset.

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type from the curated CTD Gene-Disease Associations dataset.

Split-hand/foot malformation with long bone deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Split-hand/foot malformation with long bone deficiency from the curated CTD Gene-Disease Associations dataset.

Hand Strength Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Hand Strength in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

hand, foot and mouth disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease hand, foot and mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

hand dermatosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

dermatitis, contact; hand dermatoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatitis, contact; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dermatitis, atopic; eczema; eczema allergic; hand dermatoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatitis, atopic; eczema; eczema allergic; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hand strength Gene Set

From GAD Gene-Disease Associations

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

dermatitis, allergic contact; hand dermatoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatitis, allergic contact; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart-hand syndrome, holt-oram syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dermatitis, atopic; dermatitis, irritant; dermatitis, occupational; hand dermatoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dermatitis, atopic; dermatitis, irritant; dermatitis, occupational; hand dermatoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hand Gene Set

From GeneRIF Biological Term Annotations

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

Relative hand skill in reading disability Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Relative hand skill in reading disability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

hand, foot and mouth disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease hand, foot and mouth disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

abnormality of the hand Gene Set

From GWASdb SNP-Phenotype Associations

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

sclerosis of hand bone Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal ossification of hand bones Gene Set

From HPO Gene-Disease Associations

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

irregular sclerosis of hand bones Gene Set

From HPO Gene-Disease Associations

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

bracket epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

enlarged epiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

aplasia of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

osteolytic defects of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

hypotrophy of the small hand muscles Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia involving bones of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving bones of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patchy sclerosis of hand bones Gene Set

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

hand tremor Gene Set

From HPO Gene-Disease Associations

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

enlarged epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

broad phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

valgus hand deformity Gene Set

From HPO Gene-Disease Associations

genes associated with the valgus hand deformity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

radial deviation of the hand Gene Set

From HPO Gene-Disease Associations

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

hand clenching Gene Set

From HPO Gene-Disease Associations

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

triangular epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cold-induced hand cramps Gene Set

From HPO Gene-Disease Associations

genes associated with the cold-induced hand cramps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular shaped phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

triangular shaped proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

hand muscle atrophy Gene Set

From HPO Gene-Disease Associations

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

abnormality of hand joint mobility Gene Set

From HPO Gene-Disease Associations

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

triangular epiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the hand Gene Set

From HPO Gene-Disease Associations

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

bullet-shaped phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

triangular shaped distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

absent hand Gene Set

From HPO Gene-Disease Associations

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

ulnar deviation of the hand Gene Set

From HPO Gene-Disease Associations

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

irregular ossification of hand bones Gene Set

From HPO Gene-Disease Associations

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

thimble-shaped middle phalanges of hand Gene Set

From HPO Gene-Disease Associations

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

symphalangism affecting the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

ivory epiphyses of the distal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

pseudoepiphyses of hand bones Gene Set

From HPO Gene-Disease Associations

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

bracket epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

weakness of the intrinsic hand muscles Gene Set

From HPO Gene-Disease Associations

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

hyperextensible hand joints Gene Set

From HPO Gene-Disease Associations

genes associated with the hyperextensible hand joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

osteolytic defects of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

aplasia/hypoplasia of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

joint contracture of the hand Gene Set

From HPO Gene-Disease Associations

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

cone-shaped epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

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

From HPO Gene-Disease Associations

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

synostosis involving bones of the hand Gene Set

From HPO Gene-Disease Associations

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

mesoaxial hand polydactyly Gene Set

From HPO Gene-Disease Associations

genes associated with the mesoaxial hand polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

symphalangism affecting the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormal hand morphology Gene Set

From HPO Gene-Disease Associations

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

triangular shaped middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

poor hand-eye coordination Gene Set

From HPO Gene-Disease Associations

genes associated with the poor hand-eye coordination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

small hand Gene Set

From HPO Gene-Disease Associations

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

osteolytic defects of the hand bones Gene Set

From HPO Gene-Disease Associations

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

enlarged epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

cone-shaped epiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

trident hand Gene Set

From HPO Gene-Disease Associations

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

thin proximal phalanges with broad epiphyses of the hand Gene Set

From HPO Gene-Disease Associations

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

hand polydactyly Gene Set

From HPO Gene-Disease Associations

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

cone-shaped epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

sclerosis of hand bone Gene Set

From HPO Gene-Disease Associations

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

abnormal hand bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

preaxial hand polydactyly Gene Set

From HPO Gene-Disease Associations

genes associated with the preaxial hand polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bullet-shaped middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of phalangeal joints of the hand Gene Set

From HPO Gene-Disease Associations

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

aplasia of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the epiphyses of the hand Gene Set

From HPO Gene-Disease Associations

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

radial club hand Gene Set

From HPO Gene-Disease Associations

genes associated with the radial club hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short tubular bones (hand) Gene Set

From HPO Gene-Disease Associations

genes associated with the short tubular bones (hand) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pseudoepiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

split hand Gene Set

From HPO Gene-Disease Associations

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

ivory epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

postaxial hand polydactyly Gene Set

From HPO Gene-Disease Associations

genes associated with the postaxial hand polydactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pseudoepiphyses of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

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

abnormality of the musculature of the hand Gene Set

From HPO Gene-Disease Associations

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

hand muscle weakness Gene Set

From HPO Gene-Disease Associations

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

Hand, Foot and Mouth Disease Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hand, Foot and Mouth Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hand Deformities, Congenital Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hand Deformities, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

IQ motif, EF-hand binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the IQ motif, EF-hand binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand, Ca insensitive Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand, Ca insensitive protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ISWI, HAND domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ISWI, HAND domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF hand associated, type-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF hand associated, type-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF hand associated, type-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF hand associated, type-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand domain pair Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand domain pair protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-Hand 1, calcium-binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-Hand 1, calcium-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phospholipase C, phosphoinositol-specific, EF-hand-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phospholipase C, phosphoinositol-specific, EF-hand-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Adaptor protein Cbl, EF hand-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adaptor protein Cbl, EF hand-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand calcium-binding domain-containing protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand calcium-binding domain-containing protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand domain, type 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand domain, type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

EF-hand domain, type 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the EF-hand domain, type 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

hand-foot-uterus syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the hand-foot-uterus syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

split hand/foot malformation 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split hand/foot malformation 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

split hand/foot malformation 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split hand/foot malformation 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylometaepiphyseal dysplasia, short limb-hand type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaepiphyseal dysplasia, short limb-hand type phenotype from the curated OMIM Gene-Disease Associations dataset.

?split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

heart-hand syndrome, slovenian type Gene Set

From OMIM Gene-Disease Associations

genes associated with the heart-hand syndrome, slovenian type phenotype from the curated OMIM Gene-Disease Associations dataset.

craniofacial-deafness-hand syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial-deafness-hand syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation with long bone deficiency 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation with long bone deficiency 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation with long bone deficiency 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation with long bone deficiency 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

split-hand/foot malformation 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the split-hand/foot malformation 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

hand Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

Hand Polydactyly Gene Set

From DisGeNET Gene-Disease Associations

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

Hand, Foot And Mouth Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hand, Foot And Mouth Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Broad Phalanges Of The Hand Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Broad Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Spade-Like Hand Gene Set

From DisGeNET Gene-Disease Associations

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

Recurrent Hand Flapping Gene Set

From DisGeNET Gene-Disease Associations

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

Claw Hand Gene Set

From DisGeNET Gene-Disease Associations

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

Split-Hand/Foot Malformation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Split-Hand/Foot Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hand Eczema Gene Set

From DisGeNET Gene-Disease Associations

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

Congenital Absence Of Hand Gene Set

From DisGeNET Gene-Disease Associations

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

Mesoaxial Hand Polydactyly Gene Set

From DisGeNET Gene-Disease Associations

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

Hand Monodactyly Gene Set

From DisGeNET Gene-Disease Associations

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

Split-Hand-Foot Malformation With Long Bone Deficiency 1 Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Split-Hand-Foot Malformation With Long Bone Deficiency 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Split-Hand-Foot Malformation With Sensorineural Hearing Loss Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Split-Hand-Foot Malformation With Sensorineural Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symphalangism Affecting The Phalanges Of The Hand Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Symphalangism Affecting The Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Chronic Hand Eczema Gene Set

From DisGeNET Gene-Disease Associations

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

Infected Hand Gene Set

From DisGeNET Gene-Disease Associations

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

Stereotypical Hand Wringing Gene Set

From DisGeNET Gene-Disease Associations

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

Small Epiphyses Of The Phalanges Of The Hand Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Small Epiphyses Of The Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Tenosynovitis Of Hand Gene Set

From DisGeNET Gene-Disease Associations

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

Thimble-Shaped Middle Phalanges Of Hand Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Thimble-Shaped Middle Phalanges Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormal Hand Morphology Gene Set

From DisGeNET Gene-Disease Associations

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

Radial Club Hand Gene Set

From DisGeNET Gene-Disease Associations

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

Hand Foot Uterus Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hand Foot Uterus Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Thin Proximal Phalanges With Broad Epiphyses Of The Hand Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Thin Proximal Phalanges With Broad Epiphyses Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hypotrophy Of The Small Hand Muscles Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hypotrophy Of The Small Hand Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Heart-Hand Syndrome, Slovenian Type Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Heart-Hand Syndrome, Slovenian Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Curved Distal Phalanges Of The Hand Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Curved Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bullet-Shaped Middle Phalanges Of The Hand Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bullet-Shaped Middle Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Craniofacial Deafness Hand Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Craniofacial Deafness Hand Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiminicore Disease, Moderate, With Hand Involvement Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiminicore Disease, Moderate, With Hand Involvement in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ivory Epiphyses Of The Distal Phalanges Of The Hand Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ivory Epiphyses Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Large Hand Gene Set

From DisGeNET Gene-Phenotype Associations

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

Hand Muscle Atrophy Gene Set

From DisGeNET Gene-Phenotype Associations

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

Small Hand Gene Set

From DisGeNET Gene-Phenotype Associations

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

Weakness Of The Intrinsic Hand Muscles Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Weakness Of The Intrinsic Hand Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Absence Of Hand Gene Set

From DisGeNET Gene-Phenotype Associations

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

Hand Clenching Gene Set

From DisGeNET Gene-Phenotype Associations

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

Osteolytic Defects Of The Distal Phalanges Of The Hand Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Osteolytic Defects Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Radial Deviation Of Hand Gene Set

From DisGeNET Gene-Phenotype Associations

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

Hand Muscle Weakness Gene Set

From DisGeNET Gene-Phenotype Associations

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

Aplasia Of The Proximal Phalanges Of The Hand Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Aplasia Of The Proximal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Cold-Induced Hand Cramps Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cold-Induced Hand Cramps in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Intrinsic Hand Muscle Atrophy Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Intrinsic Hand Muscle Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Hand Pain Gene Set

From DisGeNET Gene-Phenotype Associations

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

Short Tubular Bones Of The Hand Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Short Tubular Bones Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Hyperextensible Hand Joints Gene Set

From DisGeNET Gene-Phenotype Associations

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

Ivory Epiphyses Of The Phalanges Of The Hand Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ivory Epiphyses Of The Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Trident Hand Gene Set

From DisGeNET Gene-Phenotype Associations

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

Abnormal Hand Bone Ossification Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Hand Bone Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Valgus Hand Deformity Gene Set

From DisGeNET Gene-Phenotype Associations

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

Bullet-Shaped Phalanges Of The Hand Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Bullet-Shaped Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Aplasia Of The Phalanges Of The Hand Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Aplasia Of The Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Hand-Wringing Gene Set

From DisGeNET Gene-Phenotype Associations

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

Irregular Ossification Of Hand Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Irregular Ossification Of Hand Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Poor Hand-Eye Coordination Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Poor Hand-Eye Coordination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormality Of Hand Joint Mobility Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormality Of Hand Joint Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

abnormal hand joint morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal hand joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

craniofacial-deafness-hand syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease craniofacial-deafness-hand syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

hand-foot-genital syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease hand-foot-genital syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

hand, foot and mouth disease Gene Set

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

genes co-occuring with the disease hand, foot and mouth disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Focal hand dystonia Gene Set

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

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

hand-foot-genital syndrome Gene Set

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

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

Split hand-foot malformation 4 Gene Set

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

genes co-occuring with the disease Split hand-foot malformation 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Split hand-foot malformation Gene Set

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

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

craniofacial-deafness-hand syndrome Gene Set

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

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

Split hand-foot malformation 1 with sensorineural hearing loss Gene Set

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

genes co-occuring with the disease Split hand-foot malformation 1 with sensorineural hearing loss in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language Gene Set

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

genes co-occuring with the disease Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Spondylometaepiphyseal dysplasia, short limb-hand type Gene Set

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

genes co-occuring with the disease Spondylometaepiphyseal dysplasia, short limb-hand type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Split hand-foot malformation 1 Gene Set

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

genes co-occuring with the disease Split hand-foot malformation 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Split hand-foot malformation 5 Gene Set

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

genes co-occuring with the disease Split hand-foot malformation 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Split hand-foot malformation 2 Gene Set

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

genes co-occuring with the disease Split hand-foot malformation 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Split hand-foot malformation 6 Gene Set

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

genes co-occuring with the disease Split hand-foot malformation 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Hand dermatosis Gene Set

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

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

Hand Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Hand in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Split hand-foot malformation Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Split hand-foot malformation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hand muscle atrophy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hand muscle atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Heart-hand syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

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

Craniofacial-deafness-hand syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Craniofacial-deafness-hand syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hand oligodactyly Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hand oligodactyly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Aplasia/Hypoplasia of the phalanges of the hand Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Aplasia/Hypoplasia of the phalanges of the hand phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hyperextensible hand joints Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hyperextensible hand joints 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.

Hand-foot-genital syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hand-foot-genital syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

CV-A6-associated hand, foot, and mouth disease (severe vs mild) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the CV-A6-associated hand, foot, and mouth disease (severe vs mild) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Hand grip strength (Mahalanobis distance) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Hand grip strength (Mahalanobis distance) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Osteoarthritis of the hand Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Osteoarthritis of the hand phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Low hand grip strength (60 years and older) (EWGSOP) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Low hand grip strength (60 years and older) (EWGSOP) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Low hand grip strength (60 years and older) (FNIH) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Low hand grip strength (60 years and older) (FNIH) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Osteoarthritis (hand, severe) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Osteoarthritis (hand, severe) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Hand grip strength Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Hand grip strength phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Digit length ratio (right hand) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Digit length ratio (right hand) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Digit length ratio (left hand) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Digit length ratio (left hand) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Relative hand skill in reading disability Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Relative hand skill in reading disability phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Relative hand skill Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Relative hand skill phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Finger osteoarthritis severity (hand Klsum) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Finger osteoarthritis severity (hand Klsum) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Thumb osteoarthritis severity (hand Klsum) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Thumb osteoarthritis severity (hand Klsum) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.