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aplasia/hypoplasia of the distal phalanx of the thumb Gene SetFrom 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. |
aplasia/hypoplasia of the proximal phalanx of the thumb Gene SetFrom 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. |
aplasia/hypoplasia of the distal phalanx of the 5th finger Gene SetFrom 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. |
aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene SetFrom 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. |
aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene SetFrom 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. |
aplasia/hypoplasia of the distal phalanx of the 4th finger Gene SetFrom 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. |
broad distal phalanx of the thumb Gene SetFrom 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. |
bifid distal phalanx of the thumb Gene SetFrom 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. |
duplication of the distal phalanx of the thumb Gene SetFrom 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. |
abnormality of the distal phalanx of the thumb Gene SetFrom 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. |
short distal phalanx of the thumb Gene SetFrom 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. |
complete duplication of distal phalanx of the thumb Gene SetFrom 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. |
Complete Duplication Of Distal Phalanx Of The Thumb Gene SetFrom 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. |
Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb Gene SetFrom 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. |
Bifid Distal Phalanx Of The Thumb Gene SetFrom 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 SetFrom 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. |
Broad Distal Phalanx Of The Thumb Gene SetFrom 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. |
aplasia/hypoplasia of the phalanges of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the thumb 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 SetFrom 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. |
aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene SetFrom 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. |
aplasia/hypoplasia of the middle phalanx of the 5th finger Gene SetFrom 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. |
aplasia/hypoplasia of the distal phalanges of the hand Gene SetFrom 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. |
aplasia/hypoplasia of the distal phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of thumb phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
complete duplication of thumb phalanx Gene SetFrom 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. |
radial deviation of thumb terminal phalanx Gene SetFrom 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. |
complete duplication of proximal phalanx of the thumb Gene SetFrom 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. |
short phalanx of the thumb Gene SetFrom 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. |
duplication of the proximal phalanx of the thumb Gene SetFrom 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. |
absent proximal phalanx of thumb Gene SetFrom 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. |
partial duplication of thumb phalanx Gene SetFrom 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. |
short proximal phalanx of thumb Gene SetFrom 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. |
duplication of thumb phalanx Gene SetFrom 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. |
abnormality of the proximal phalanx of the thumb Gene SetFrom 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. |
Duplication Of Thumb Phalanx Gene SetFrom 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. |
Partial Duplication Of Thumb Phalanx Gene SetFrom 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 SetFrom 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. |
Radial Deviation Of Thumb Terminal Phalanx Gene SetFrom 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. |
Complete Duplication Of Thumb Phalanx Gene SetFrom 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. |
Absent Proximal Phalanx Of Thumb Gene SetFrom 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. |
Abnormality Of The Proximal Phalanx Of The Thumb Gene SetFrom 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. |
Triangular shaped proximal phalanx of the thumb Gene SetFrom 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. |
Thumb Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thumb Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
dysplastic distal thumb phalanges with a central hole Gene SetFrom HPO Gene-Disease Associations genes associated with the dysplastic distal thumb phalanges with a central hole phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Dysplastic Distal Thumb Phalanges With A Central Hole Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dysplastic Distal Thumb Phalanges With A Central Hole in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
aplasia of the middle phalanx of the hand Gene SetFrom 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. |
short distal phalanx of finger Gene SetFrom 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. |
duplication of distal phalanx of toe Gene SetFrom 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. |
duplication of the distal phalanx of hand Gene SetFrom 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. |
abnormality of the epiphyses of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the 3rd finger Gene SetFrom 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. |
sclerosis of distal finger phalanx Gene SetFrom 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. |
partial duplication of the distal phalanx of the 3rd finger Gene SetFrom 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. |
partial duplication of the distal phalanx of the 2nd finger Gene SetFrom 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. |
slender distal phalanx of finger Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
broad distal phalanx of the toes Gene SetFrom 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. |
broad distal phalanx of the hallux Gene SetFrom 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. |
abnormality of the distal phalanx of the 5th finger Gene SetFrom 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 SetFrom 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. |
fifth finger distal phalanx clinodactyly Gene SetFrom 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 SetFrom 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. |
duplication of the distal phalanx of the hallux Gene SetFrom 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. |
short distal phalanx of the 5th finger Gene SetFrom 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. |
long distal phalanx of finger Gene SetFrom 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. |
partial duplication of the distal phalanx of the hallux Gene SetFrom 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. |
bifid distal phalanx of toe Gene SetFrom 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 SetFrom 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. |
short distal phalanx of the 2nd finger Gene SetFrom 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. |
short distal phalanx of the 4th finger Gene SetFrom 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. |
duplication of the distal phalanx of the 2nd finger Gene SetFrom 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. |
abnormality of the distal phalanx of finger Gene SetFrom 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 distal phalanx of the 2nd finger Gene SetFrom 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. |
Short Distal Phalanx Gene SetFrom 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. |
Fifth Finger Distal Phalanx Clinodactyly Gene SetFrom 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. |
Triangular Shaped Distal Phalanx Gene SetFrom 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 SetFrom 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. |
Partial Duplication Of The Distal Phalanx Of The 2Nd Finger Gene SetFrom 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 SetFrom 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. |
Broad Distal Phalanx Of The Hallux Gene SetFrom 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 SetFrom 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. |
Bullet-Shaped Distal Phalanx Of The Hallux Gene SetFrom 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 SetFrom 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. |
Broad Distal Phalanx Of Finger Gene SetFrom 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. |
Partial Duplication Of The Distal Phalanx Of The Hallux Gene SetFrom 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. |
Duplication Of The Distal Phalanx Of Hand Gene SetFrom 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. |
Slender Distal Phalanx Of Finger Gene SetFrom 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. |
aplasia/hypoplasia involving the central nervous system Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aplasia/hypoplasia of the cerebrum Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the aplasia/hypoplasia of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
aplasia/hypoplasia of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the fallopian tube Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the uvula Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the uvula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the tragus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tragus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the nose Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the frontal sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the lungs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the lungs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the quadriceps Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the quadriceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the musculature of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the scapulae Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the scapulae 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 SetFrom 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 of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the hand Gene SetFrom 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. |
aplasia/hypoplasia of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the iris Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the pyramidal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving forearm bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving forearm bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the sternum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the optic nerve Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the ovary Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the corticospinal tracts Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the tarsal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the feet Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the biceps Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the biceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the fundus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the fundus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the retina Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the retina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the gallbladder Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the gallbladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the pelvis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the mandible Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the epiglottis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of metatarsal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of metatarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the uterus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the eyebrow Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the spleen Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the choroid Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the triceps Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the triceps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal hypoplasia/aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the renal hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting bones of the axial skeleton Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting bones of the axial skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 1st metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the earlobes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the earlobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 4th metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cerebellar vermis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 2nd metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 2nd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the skeleton Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the humerus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the palmar creases Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the maxilla Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the maxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the ribs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 1st metatarsal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 1st metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the vertebral column Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the metacarpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the nipples Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nipples phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 5th metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the ear Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the diaphragm Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the premaxilla Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cerebrum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 3rd toe Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd toe 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 SetFrom 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. |
aplasia/hypoplasia of the phalanges of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the uvea Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the uvea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the sweat glands Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the femur Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the anterior segment of the eye Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the nasal bone Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the middle phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the testes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the testes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the thorax Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the optic tract Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the nails Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the brainstem Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the abdominal wall musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the fovea Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fovea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cochlea Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the sinuses Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the femoral head and neck 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 SetFrom 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. |
aplasia/hypoplasia of the extremities Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the nasal septum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the clavicles Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the clavicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the sacrum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the sacrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the skull Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the skull phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the musculature of the pelvis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the musculature of the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the tibia Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tibia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the patella Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the patella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the skeletal musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the skeletal musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the central nervous system Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia affecting the eyelid Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia affecting the eyelid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the vagina Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the breasts Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the breasts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the musculature of the extremities Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the pubic bone Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the pancreas Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the pancreas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cervical spine Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cervical spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the cerebellum Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebellum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the lens Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the lens phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the external ear Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the external ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the shoulder musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the shoulder musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the musculature of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the tongue Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the tongue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the colon Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the colon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 3rd metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pectoral muscle hypoplasia/aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pectoral muscle hypoplasia/aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the macula Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the macula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the musculature of the thigh Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the musculature of the thigh phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the fibula Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
patella aplasia or hypoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the patella aplasia or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
?breasts and/or nipples, aplasia or hypoplasia of, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?breasts and/or nipples, aplasia or hypoplasia of, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The Thymus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Thymus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pectoral Muscle Hypoplasia/Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pectoral Muscle Hypoplasia/Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The Iris Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Iris in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The Earlobes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Earlobes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The Capital Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Capital Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The Extremities Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Extremities in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Breasts And/Or Nipples, Aplasia Or Hypoplasia Of, 2 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Breasts And/Or Nipples, Aplasia Or Hypoplasia Of, 2 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The 5Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The Abdominal Wall Musculature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Abdominal Wall Musculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Eyebrow Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Eyebrow in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Breasts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Breasts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Nails Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Nails in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Cerebellar Vermis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Corpus Callosum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Cerebellum Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Cerebellum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Frontal Sinuses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Frontal Sinuses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Skin Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Skin in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Renal Hypoplasia/Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Renal Hypoplasia/Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Fallopian Tube Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Fallopian Tube in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Involving The Central Nervous System Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Involving The Skeletal Musculature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Skeletal Musculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Tongue Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Uterus Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Involving The Metacarpal Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Metacarpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The 1St Metacarpal Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The 1St Metacarpal in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of Fingers Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Uvula Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Uvula in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Nipples Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Nipples in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Lungs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Lungs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Involving The Pelvis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Pelvis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The 3Rd Toe Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The 3Rd Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Affecting The Eye Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Affecting The Eye in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The External Ear Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The External Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Clavicles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Clavicles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Diaphragm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Diaphragm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Gallbladder Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Gallbladder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of Metatarsal Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of Metatarsal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Involving The Nose Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Vagina Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Vagina in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Pancreas Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Pancreas in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Lens Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Lens in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Optic Nerve Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Optic Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Involving The Carpal Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Involving The Carpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia Of The Testes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Testes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia/Hypoplasia of the phalanges of the hand Gene SetFrom 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. |
Aplasia/Hypoplasia involving the metacarpal bones Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aplasia/Hypoplasia involving the metacarpal bones phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aplasia/Hypoplasia of the corpus callosum Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aplasia/Hypoplasia of the corpus callosum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Aplasia/Hypoplasia of the cerebellum Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Aplasia/Hypoplasia of the cerebellum phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
distal ulnar hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the distal ulnar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Distal Ulnar Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Ulnar Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Stapes ankylosis with broad thumb and toes Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Stapes ankylosis with broad thumb and toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
STAPES ANKYLOSIS WITH BROAD THUMB AND TOES Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease STAPES ANKYLOSIS WITH BROAD THUMB AND TOES from the curated CTD Gene-Disease Associations dataset. |
thumb Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term thumb in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormality of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the absent thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flexion contracture of thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the flexion contracture of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal placement of thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal placement of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the broad thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
opposable triphalangeal thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the opposable triphalangeal thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hitchhiker thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the hitchhiker thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the short thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial absence of thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the partial absence of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adducted thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the adducted thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triphalangeal thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the triphalangeal thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
contractures of the interphalangeal joint of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the contractures of the interphalangeal joint of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
DNA polymerase beta, thumb domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA polymerase beta, thumb domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
triphalangeal thumb-polysyndactyly syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the triphalangeal thumb-polysyndactyly syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
stapes ankylosis with broad thumb and toes Gene SetFrom OMIM Gene-Disease Associations genes associated with the stapes ankylosis with broad thumb and toes phenotype from the curated OMIM Gene-Disease Associations dataset. |
triphalangeal thumb, type i Gene SetFrom OMIM Gene-Disease Associations genes associated with the triphalangeal thumb, type i phenotype from the curated OMIM Gene-Disease Associations dataset. |
Triphalangeal Thumb Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Triphalangeal Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thumb In Palm Deformity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thumb In Palm Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hitch-Hiker Thumb Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hitch-Hiker Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Stapes Ankylosis With Broad Thumb And Toes (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stapes Ankylosis With Broad Thumb And Toes (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Opposable Triphalangeal Thumb Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Opposable Triphalangeal Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tibial Hemimelia, Polysyndactyly, Triphalangeal Thumb Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tibial Hemimelia, Polysyndactyly, Triphalangeal Thumb Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adducted Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adducted Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Placement Of Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Placement Of Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thumb Deformity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thumb Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thumb Absent Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thumb Absent in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hyperextensible Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyperextensible Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Deviation Of The Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deviation Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distally Placed Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distally Placed Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Thumb, Bilateral Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Thumb, Bilateral in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Triphalangeal thumb-polysyndactyly syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Triphalangeal thumb-polysyndactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Polydactyly of a triphalangeal thumb Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Polydactyly of a triphalangeal thumb phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thumb deformity Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thumb deformity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Polydactyly of a biphalangeal thumb Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Polydactyly of a biphalangeal thumb phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thumb osteoarthritis severity (hand Klsum) Gene SetFrom 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. |
abnormality of phalanx of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
sclerosis of finger phalanx Gene SetFrom 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 SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of phalanx of toe Gene SetFrom 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. |
broad phalanx of the toes Gene SetFrom 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. |
symphalangism of middle phalanx of finger Gene SetFrom 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. |
bracket epiphysis of the middle phalanx of the 2nd finger Gene SetFrom 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 SetFrom 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 SetFrom 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. |
patchy sclerosis of finger phalanx Gene SetFrom 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. |
triangular shaped middle phalanx of the 5th finger Gene SetFrom 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. |
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender proximal phalanx of finger Gene SetFrom 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 SetFrom 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. |
triangular shaped proximal phalanx of the 3rd finger Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
symphalangism of middle phalanx of 5th finger Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
short middle phalanx of finger Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
complete duplication of phalanx of hand Gene SetFrom HPO Gene-Disease Associations genes associated with the complete duplication of phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of middle phalanx of toe Gene SetFrom 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 SetFrom 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. |
short middle phalanx of the 5th finger Gene SetFrom 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 SetFrom 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. |
duplication of phalanx of hand Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of phalanx of 2nd finger Gene SetFrom 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. |
triangular shaped middle phalanx of the 2nd finger Gene SetFrom 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. |
triangular epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom 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. |
triangular epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
short middle phalanx of the 2nd finger Gene SetFrom 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 SetFrom 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. |
abnormality of the proximal phalanx of the 2nd finger Gene SetFrom 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. |
duplication of the middle phalanx of hand Gene SetFrom 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. |
short phalanx of finger Gene SetFrom 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. |
duplication of the proximal phalanx of the hallux Gene SetFrom 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. |
short proximal phalanx of hallux Gene SetFrom 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. |
short phalanx of hallux Gene SetFrom 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. |
symphalangism affecting the proximal phalanx of the 5th finger Gene SetFrom 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. |
abnormality of the epiphysis of the middle phalanx of the 2nd finger Gene SetFrom 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 SetFrom 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 SetFrom 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. |
enlarged epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom 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. |
partial duplication of the phalanx of hand Gene SetFrom 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. |
sclerosis of finger phalanx Gene SetFrom 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 epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
duplication of phalanx of hallux Gene SetFrom 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. |
abnormality of the proximal phalanx of the 3rd finger Gene SetFrom 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 SetFrom 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. |
abnormal phalanx morphology Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Broad Middle Phalanx Of Finger Gene SetFrom 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. |
Short Middle Phalanx Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Long Proximal Phalanx Of Finger Gene SetFrom 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 SetFrom 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. |
Duplication Of The Proximal Phalanx Of The Hallux Gene SetFrom 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. |
Short Phalanx Of Finger Gene SetFrom 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 Phalanx Of The Toes Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Complete Duplication Of The Middle Phalanx Of The 3Rd Finger Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Absent Middle Phalanx Of 5Th Finger Gene SetFrom 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 SetFrom 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 SetFrom 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. |
Complete Duplication Of Hallux Phalanx Gene SetFrom 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. |
Broad Proximal Phalanx Of The Hallux Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
Renal hypodysplasia/aplasia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal hypodysplasia/aplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Deafness with labyrinthine aplasia microtia and microdontia (LAMM) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Deafness with labyrinthine aplasia microtia and microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mullerian aplasia and hyperandrogenism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aplasia cutis congenita Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Radial aplasia-thrombocytopenia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Radial aplasia-thrombocytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic nerve aplasia, bilateral Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic nerve aplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital bilateral aplasia of vas deferens Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital bilateral aplasia of vas deferens from the curated CTD Gene-Disease Associations dataset. |
Red-Cell Aplasia, Pure Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Red-Cell Aplasia, Pure from the curated CTD Gene-Disease Associations dataset. |
Craniosynostosis radial aplasia syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Craniosynostosis radial aplasia syndrome from the curated CTD Gene-Disease Associations dataset. |
Aplasia of Lacrimal and Salivary Glands Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aplasia of Lacrimal and Salivary Glands from the curated CTD Gene-Disease Associations dataset. |
Mullerian Aplasia and Hyperandrogenism Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mullerian Aplasia and Hyperandrogenism from the curated CTD Gene-Disease Associations dataset. |
pure red-cell aplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pure red-cell aplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
anemia; kidney diseases; red-cell aplasia, pure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia; kidney diseases; red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
red-cell aplasia, pure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease red-cell aplasia, pure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aplasia Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term aplasia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
aplasia of the inferior half of the cerebellar vermis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the inferior half of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia cutis congenita of scalp Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia cutis congenita of scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the uterus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lacrimal gland aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the lacrimal gland aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the tarsal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the tarsal bones 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 SetFrom 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. |
biceps aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the biceps aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mandibular aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the mandibular aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the abdominal wall musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lacrimal duct aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the lacrimal duct aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of metacarpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of metacarpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia cutis congenita over posterior parietal area Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia cutis congenita over posterior parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
patellar aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the patellar aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the ovary Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplastia of the eccrine sweat glands Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplastia of the eccrine sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the semicircular canal Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the semicircular canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mandibular condyle aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the mandibular condyle aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
quadriceps aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the quadriceps aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the nose Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia cutis congenita Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia cutis congenita phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bilateral radial aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the bilateral radial aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the epiglottis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the testes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the testes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
carpal bone aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the carpal bone aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the sweat glands Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peripheral pulmonary vessel aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the peripheral pulmonary vessel aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
midclavicular aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the midclavicular aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia cutis congenita over the scalp vertex Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia cutis congenita over the scalp vertex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the pectoralis major muscle Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the pectoralis major muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triceps aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the triceps aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anterior segment of eye aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the anterior segment of eye aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the optic tract Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the optic tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the vagina Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia cutis congenita on trunk or limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia cutis congenita on trunk or limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia involving bones of the lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia involving bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the parotid gland Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the parotid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia involving bones of the extremities Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia involving bones of the extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia involving forearm bones Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia involving forearm bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
breast aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the breast aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the inner ear Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the phalanges of the hand Gene SetFrom 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. |
aplasia cutis congenita over parietal area Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia cutis congenita over parietal area phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia involving bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fibular aplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the fibular aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal hypodysplasia/aplasia 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal hypodysplasia/aplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aplasia of lacrimal and salivary glands Gene SetFrom OMIM Gene-Disease Associations genes associated with the aplasia of lacrimal and salivary glands phenotype from the curated OMIM Gene-Disease Associations dataset. |
?renal hypodysplasia/aplasia 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?renal hypodysplasia/aplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
mullerian aplasia and hyperandrogenism Gene SetFrom OMIM Gene-Disease Associations genes associated with the mullerian aplasia and hyperandrogenism phenotype from the curated OMIM Gene-Disease Associations dataset. |
aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies Gene SetFrom OMIM Gene-Disease Associations genes associated with the aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies phenotype from the curated OMIM Gene-Disease Associations dataset. |
?aplasia cutis congenita, nonsyndromic Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?aplasia cutis congenita, nonsyndromic phenotype from the curated OMIM Gene-Disease Associations dataset. |
Aplasia Of The Semicircular Canal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Semicircular Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Cutis Congenita Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pure Red-Cell Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pure Red-Cell Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tibial Aplasia And Ectrodactyly Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tibial Aplasia And Ectrodactyly Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Aplasia Of The Vermis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Aplasia Of The Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Bilateral Aplasia Of Vas Deferens Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Bilateral Aplasia Of Vas Deferens in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vas Deferens, Congenital Bilarteral, Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vas Deferens, Congenital Bilarteral, Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Renal Dysplasia And Retinal Aplasia (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Renal Dysplasia And Retinal Aplasia (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Cutis Congenita Of Scalp Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita Of Scalp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Cutis Congenita Over Posterior Parietal Area Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita Over Posterior Parietal Area in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Of The Bone Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
B-Cell Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease B-Cell Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Optic Nerve Aplasia, Bilateral Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Optic Nerve Aplasia, Bilateral in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Cutis Congenita Over The Scalp Vertex Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita Over The Scalp Vertex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Of The Epiglottis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Epiglottis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Of Muscle Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mullerian Aplasia And Hyperandrogenism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mullerian Aplasia And Hyperandrogenism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hydranencephaly With Renal Aplasia-Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hydranencephaly With Renal Aplasia-Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Radial Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Radial Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Aplasia Of Inner Ear Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Aplasia Of Inner Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplastia Of The Eccrine Sweat Glands Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplastia Of The Eccrine Sweat Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Of Lacrimal And Salivary Glands Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of Lacrimal And Salivary Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Of The Parotid Gland Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Parotid Gland in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lacrimal Duct Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lacrimal Duct Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Mullerian Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Mullerian Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Cutis Congenita With Epibulbar Dermoids Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Cutis Congenita With Epibulbar Dermoids in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Of The Pectoralis Major Muscle Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia Of The Pectoralis Major Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Wilms Tumor And Radial Bilateral Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Wilms Tumor And Radial Bilateral Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Patellar Aplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Patellar Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia Of The Bone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fibular Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibular Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Cutis Congenita On Trunk Or Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Cutis Congenita On Trunk Or Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Patellar Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Patellar Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of The Proximal Phalanges Of The Hand Gene SetFrom 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. |
Aplasia Of The Abdominal Wall Musculature Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Abdominal Wall Musculature in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of The Sweat Glands Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Sweat Glands in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of Optic Nerve Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of Optic Nerve in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mandibular Condyle Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mandibular Condyle Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of The Ulna Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Ulna in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lacrimal Gland Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lacrimal Gland Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Anterior Segment Of Eye Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Anterior Segment Of Eye Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of The Bladder Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Bladder in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pancreatic Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pancreatic Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of Metacarpal Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of Metacarpal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of The Phalanges Of The Hand Gene SetFrom 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. |
Aplasia Of The Tarsal Bones Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Tarsal Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Carpal Bone Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Carpal Bone Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of The Phalanges Of The 3Rd Toe Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Phalanges Of The 3Rd Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Biceps Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Biceps Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Quadriceps Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Quadriceps Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Triceps Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Triceps Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of The Vagina Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Vagina in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Midclavicular Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Midclavicular Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bilateral Radial Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bilateral Radial Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Unilateral Radial Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unilateral Radial Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Aplasia Of The Inferior Half Of The Cerebellar Vermis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Inferior Half Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peripheral Pulmonary Vessel Aplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Pulmonary Vessel Aplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pure red-cell aplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Pure red-cell aplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Mullerian aplasia and hyperandrogenism Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Mullerian aplasia and hyperandrogenism from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Mullerian aplasia and hyperandrogenism Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mullerian aplasia and hyperandrogenism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bilateral renal aplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bilateral renal aplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pure red-cell aplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pure red-cell aplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Aplasia of lacrimal and salivary glands Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Aplasia of lacrimal and salivary glands in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Renal hypodysplasia/aplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal hypodysplasia/aplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Renal dysplasia and retinal aplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Renal dysplasia and retinal aplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Congenital bilateral aplasia of vas deferens from CFTR mutation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital bilateral aplasia of vas deferens from CFTR mutation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Radial aplasia-thrombocytopenia syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Radial aplasia-thrombocytopenia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant aplasia and myelodysplasia Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant aplasia and myelodysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Mullerian aplasia and hyperandrogenism Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Mullerian aplasia and hyperandrogenism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal hereditary motor neuronopathy 2D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, X-linked 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, with normal red cell morphology Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with normal red cell morphology phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal myopathy Markesbery-Griggs type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal myopathy Markesbery-Griggs type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 5B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal arthrogryposis type 1B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal arthrogryposis type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 7B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, with hemolytic anemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal arthrogryposis type 2B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal arthrogryposis type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, distal, type 5d Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, distal, type 5d phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, autosomal recessive 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, Distal, with Anterior Tibial Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset. |
Welander distal myopathy, Swedish type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Welander distal myopathy, Swedish type from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Distal Hereditary Motor, Type IIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type IIA from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Distal, With Hemolytic Anemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, With Hemolytic Anemia from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type V Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type V from the curated CTD Gene-Disease Associations dataset. |
Jacobsen Distal 11q Deletion Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Jacobsen Distal 11q Deletion Syndrome from the curated CTD Gene-Disease Associations dataset. |
Renal tubular acidosis, distal, autosomal recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal tubular acidosis, distal, autosomal recessive from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type IIB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type IIB from the curated CTD Gene-Disease Associations dataset. |
Arthrogryposis, Distal, Type 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis, Distal, Type 4 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset. |
ARTHROGRYPOSIS, DISTAL, TYPE 1A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ARTHROGRYPOSIS, DISTAL, TYPE 1A from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness from the curated CTD Gene-Disease Associations dataset. |
Distal myopathy, Nonaka type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal myopathy, Nonaka type from the curated CTD Gene-Disease Associations dataset. |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Distal Hereditary Motor, Type VIIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset. |
Arthrogryposis multiplex congenita, distal, X-linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis multiplex congenita, distal, X-linked from the curated CTD Gene-Disease Associations dataset. |
Distal Myopathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal Myopathies from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type Viib Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type Viib from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset. |
Distal arthrogryposis type 2B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal arthrogryposis type 2B from the curated CTD Gene-Disease Associations dataset. |
distal muscular dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
distal hereditary motor neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal hereditary motor neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
distal arthrogryposis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal arthrogryposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial distal renal tubular acidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
proximal chromosome 9p to q and distal chromosome 9q Gene SetFrom GAD Gene-Disease Associations genes associated with the disease proximal chromosome 9p to q and distal chromosome 9q in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
distal myopathies; myositis, inclusion body Gene SetFrom GAD Gene-Disease Associations genes associated with the disease distal myopathies; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
distal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term distal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
proximal/distal pattern formation involved in nephron development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in nephron development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
proximal/distal pattern formation involved in metanephric nephron development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in metanephric nephron development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric distal tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
distal tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
lung proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lung proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
polarity specification of proximal/distal axis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the polarity specification of proximal/distal axis biological process from the curated GO Biological Process Annotations 2015 dataset. |
proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
proximal/distal pattern formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in positive regulation of transcription Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in positive regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in negative regulation of transcription Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in negative regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
wide tufts of distal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the wide tufts of distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapering pointed ends of distal finger phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the tapering pointed ends of distal finger phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal upper limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal upper limb muscle weakness 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 SetFrom 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. |
distal widening of metacarpals Gene SetFrom HPO Gene-Disease Associations genes associated with the distal widening of metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
late-onset distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the late-onset distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired distal vibration sensation Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired distal vibration sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanges of the hand Gene SetFrom 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. |
impaired distal tactile sensation Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired distal tactile sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanges of all fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanges of all fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
trapezoidal distal femoral condyles Gene SetFrom HPO Gene-Disease Associations genes associated with the trapezoidal distal femoral condyles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
widened distal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the widened distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the small distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene SetFrom HPO Gene-Disease Associations genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent distal interphalangeal creases Gene SetFrom HPO Gene-Disease Associations genes associated with the absent distal interphalangeal creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped distal phalanges of the hand Gene SetFrom 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. |
progressive distal muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal upper limb amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal lower limb amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal lower limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal lower limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased distal sensory nerve action potential Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased distal sensory nerve action potential phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal femoral metaphyseal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the distal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal tapering of metatarsals Gene SetFrom HPO Gene-Disease Associations genes associated with the distal tapering of metatarsals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal ileal atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the distal ileal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal tapering femur Gene SetFrom HPO Gene-Disease Associations genes associated with the distal tapering femur 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 SetFrom 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. |
hypoplastic distal humeri Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplastic distal humeri 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 SetFrom 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. |
distal amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
wide distal femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the wide distal femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal shortening of limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the distal shortening of limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteolytic defects of the distal phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the osteolytic defects of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal sensory impairment of all modalities Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory impairment of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
club-shaped distal femur Gene SetFrom HPO Gene-Disease Associations genes associated with the club-shaped distal femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shortening of all distal phalanges of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the shortening of all distal phalanges of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal/middle symphalangism of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the distal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal femoral bowing Gene SetFrom HPO Gene-Disease Associations genes associated with the distal femoral bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent distal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the absent distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal symphalangism Gene SetFrom HPO Gene-Disease Associations genes associated with the distal symphalangism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized distal tubular acidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized distal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypermobility of distal interphalangeal joints Gene SetFrom HPO Gene-Disease Associations genes associated with the hypermobility of distal interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
irregular distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the irregular distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal renal tubular acidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the distal renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal sensory impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapered distal phalanges of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the tapered distal phalanges of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal peripheral sensory neuropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal peripheral sensory neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
acroosteolysis of distal phalanges (feet) Gene SetFrom HPO Gene-Disease Associations genes associated with the acroosteolysis of distal phalanges (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal tibial bowing Gene SetFrom HPO Gene-Disease Associations genes associated with the distal tibial bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal urethral duplication Gene SetFrom 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. |
distal sensory loss of all modalities Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory loss of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlargement of the distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the enlargement of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal arthrogryposis Gene SetFrom HPO Gene-Disease Associations genes associated with the distal arthrogryposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal symphalangism (hands) Gene SetFrom HPO Gene-Disease Associations genes associated with the distal symphalangism (hands) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired distal proprioception Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired distal proprioception phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent fourth finger distal interphalangeal crease Gene SetFrom HPO Gene-Disease Associations genes associated with the absent fourth finger distal interphalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Distal-less-like homeobox protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Distal-less-like homeobox protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
dilated distal convoluted tubules Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated distal convoluted tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal distal convoluted tubule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal distal convoluted tubule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal distal visceral endoderm morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal distal visceral endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal proximal-distal axis patterning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent distal visceral endoderm Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent distal visceral endoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
chromosome 7q11.23 deletion syndrome, distal, 1.2mb Gene SetFrom OMIM Gene-Disease Associations genes associated with the chromosome 7q11.23 deletion syndrome, distal, 1.2mb phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type vi Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vi phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type vb Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vb phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type viia Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type viia phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, chronic distal, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type iid Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type iid phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthyrgryposis, distal, type 2b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthyrgryposis, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset. |
chromosome 22q11.2 deletion syndrome, distal Gene SetFrom OMIM Gene-Disease Associations genes associated with the chromosome 22q11.2 deletion syndrome, distal phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, jerash type Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, jerash type phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 2b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 2a Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset. |
welander distal myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the welander distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal tubular acidosis, distal, ar Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, ar phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal tubular acidosis, distal, ad Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, ad phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
laing distal myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the laing distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neuronopathy, distal hereditary motor, type iic Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neuronopathy, distal hereditary motor, type iic phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type va Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal tubular acidosis, distal, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis multiplex congenita, distal, type 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, distal, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis multiplex congenita, distal, type 2b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, with anterior tibial onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, x-linked 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type viib Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 1b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, congenital nonprogressive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 5d Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 5d phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, tateyama type Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, tateyama type phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type iib Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iib phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type iia Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset. |
distal tip Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tip in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
distal tubular epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tubular epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
renal distal tubule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue renal distal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
distal tip cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tip cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Distal Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Arthrogryposis Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Arthrogryposis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Lower Limb Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Lower Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Jacobsen Distal 11Q Deletion Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Jacobsen Distal 11Q Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Renal Tubular Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Distal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 3P Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 3P Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodic Paralysis With Later-Onset Distal Motor Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodic Paralysis With Later-Onset Distal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Distal Phalanges Of All Fingers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Distal Phalanges Of All Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chromosome 22Q11.2 Deletion Syndrome, Distal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 22Q11.2 Deletion Syndrome, Distal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Welander Distal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Welander Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Upper Limb Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Ileal Obstruction Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Ileal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Intestinal Obstruction Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Intestinal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Tibial Bowing Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Tibial Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Irregular Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Irregular Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Flat Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Flat Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Bile Duct Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tapering Pointed Ends Of Distal Finger Phalanges Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tapering Pointed Ends Of Distal Finger Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Hereditary Motor Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Hereditary Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Peripheral Sensory Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Peripheral Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Arthrogryposis Type 5D Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Arthrogryposis Type 5D in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 12P Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 12P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Tapering Femur Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Tapering Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Distal Tubular Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Distal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Colitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Colitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Urethral Duplication Gene SetFrom 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. |
Klhl9-Related Early-Onset Distal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Klhl9-Related Early-Onset Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Bile Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complete Duplication Of The Distal Phalanges Of The Hand Gene SetFrom 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. |
Acroosteolysis Of Distal Phalanges (Feet) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acroosteolysis Of Distal Phalanges (Feet) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Curved Distal Phalanges Of The Hand Gene SetFrom 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. |
Distal Myopathy 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Myopathy 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Tapering Of Metatarsals Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Tapering Of Metatarsals in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Trisomy 10Q Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Trisomy 10Q Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Absent Fourth Finger Distal Interphalangeal Crease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Absent Fourth Finger Distal Interphalangeal Crease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyperkalemic Distal Renal Tubular Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyperkalemic Distal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal-Type Epithelioid Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal-Type Epithelioid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ivory Epiphyses Of The Distal Phalanges Of The Hand Gene SetFrom 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. |
Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal 17P13.3 Microdeletion Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal 17P13.3 Microdeletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 1Q Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 1Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 13Q Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 13Q Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chromosome 19Q13.11 Deletion Syndrome, Distal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 19Q13.11 Deletion Syndrome, Distal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Sensory Impairment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Sensory Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Impaired Distal Proprioception Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Proprioception in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Muscle Atrophy Due To Neurologic Disease Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Atrophy Due To Neurologic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Shortening Of All Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shortening Of All Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Distal Limb Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Distal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Late-Onset Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Lower Limb Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Lower Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Upper Limb Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Upper Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Club-Shaped Distal Femur Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Club-Shaped Distal Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Sensory Impairment Of All Modalities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Sensory Impairment Of All Modalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Renal Tubular Acidosis Co-Occurrent With Sensorineural Deafness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Renal Tubular Acidosis Co-Occurrent With Sensorineural Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Osteolytic Defects Of The Distal Phalanges Of The Hand Gene SetFrom 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. |
Impaired Distal Vibration Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Vibration Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Small Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Wide Tufts Of Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Tufts Of Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hypermobility Of Distal Interphalangeal Joints Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypermobility Of Distal Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Joint Laxity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Joint Laxity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Impaired Distal Tactile Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Tactile Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Ileal Atresia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Ileal Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Femoral Bowing Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Femoral Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tapered Distal Phalanges Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tapered Distal Phalanges Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Distal Hallux Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Widened Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widened Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Shortening Of Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Shortening Of Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Distal Interphalangeal Creases Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Distal Interphalangeal Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Enlargement Of The Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlargement Of The Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Acroosteolysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Acroosteolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Distal Sensory Nerve Action Potential Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Distal Sensory Nerve Action Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Widening Of Metacarpals Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Widening Of Metacarpals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Trapezoidal Distal Femoral Condyles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Trapezoidal Distal Femoral Condyles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Wide Distal Femoral Metaphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Distal Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal/Middle Symphalangism Of 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal/Middle Symphalangism Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
proximal/distal pattern formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric distal tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal dendrite Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the distal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
apical distal dendrite Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the apical distal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
dilated distal convoluted tubule Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated distal convoluted tubule phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal distal convoluted tubule morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal distal convoluted tubule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal proximal-distal axis patterning Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal distal visceral endoderm morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal distal visceral endoderm morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent distal visceral endoderm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent distal visceral endoderm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased distal limb length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased distal limb length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Kidney - L1 - Distal Convoluted Tubule Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L1 - Distal Convoluted Tubule cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Distal Convoluted Tubule Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Distal Convoluted Tubule cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Distal Convoluted Tubule Type 1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Distal Convoluted Tubule Type 1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Distal Convoluted Tubule Type 2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Distal Convoluted Tubule Type 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Distal epithelial cell_Distal airway_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal epithelial cell_Distal airway_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal Proliferative Progenitor cell_Bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal Proliferative Progenitor cell_Bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal limb bud cell_Limb bud_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal limb bud cell_Limb bud_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Enterocyte distal cell_Intestine_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Enterocyte distal cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal stem cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal stem cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal convoluted tubular cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubule & loop of Henle cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubule & loop of Henle cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubular cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Medial and distal segment cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Medial and distal segment cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubular cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubular cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal convoluted tubular cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal cell_Blood vessel_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Blood vessel_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal lung progenitor cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal lung progenitor cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal epithelial cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal epithelial cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal cell_Prostate_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Prostate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal convoluted tubular cell_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
16p11 2 distal deletion syndrome Gene SetFrom WikiPathways Pathways 2024 proteins participating in the 16p11 2 distal deletion syndrome pathway from the WikiPathways Pathways 2024 dataset. |
7q11 23 distal copy number variation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the 7q11 23 distal copy number variation pathway from the WikiPathways Pathways 2024 dataset. |
Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) Gene Setproteins participating in the Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) pathway from the Reactome Pathways 2024 dataset. |
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5619114 Gene Setproteins participating in the Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5619114 pathway from the Reactome Pathways 2024 dataset. |
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5658471 Gene Setproteins participating in the Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5658471 pathway from the Reactome Pathways 2024 dataset. |
proximal/distal pattern formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric distal tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal dendrite Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the distal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
apical distal dendrite Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the apical distal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Distal arthrogryposis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive distal hereditary motor neuronopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis type 2B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal 10q deletion syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal 10q deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal myopathy 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal arthrogryposis type 5D Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 5D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy with rimmed vacuoles Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with rimmed vacuoles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy with anterior tibial onset Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with anterior tibial onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 14 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chromosome 22q11.2 deletion syndrome, distal Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 22q11.2 deletion syndrome, distal in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 9 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked distal spinal muscular atrophy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked distal spinal muscular atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 10 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1C Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Partial trisomy distal 4q Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial trisomy distal 4q in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal 10q deletion syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal 10q deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Renal distal tubule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal distal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal tip cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tip cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal tip Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tip in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal tubular epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tubular epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal axon Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal axon cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Distal portion of axoneme Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal portion of axoneme cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Distal dendrite Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Apical distal dendrite Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Apical distal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor distal connecting cilium Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Photoreceptor distal connecting cilium cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Distal axon Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal axon cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Distal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor distal connecting cilium Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Photoreceptor distal connecting cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Distal portion of axoneme Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal portion of axoneme cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Basal distal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Basal distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Apical distal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Apical distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
bacterial-type flagellum basal body, distal rod, L ring Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the bacterial-type flagellum basal body, distal rod, L ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
bacterial-type flagellum basal body, distal rod Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the bacterial-type flagellum basal body, distal rod cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive distal renal tubular acidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive distal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal renal tubular acidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal arthrogryposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal arthrogryposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal lower limb muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal lower limb muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal lower limb amyotrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal lower limb amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal hereditary motor neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal hereditary motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant distal renal tubular acidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive scapulohumeroperoneal distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive scapulohumeroperoneal distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Arthrogryposis multiplex congenita distal Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis multiplex congenita distal phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Welander distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Welander distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal shortening of limbs Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal shortening of limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Finnish upper limb-onset distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish upper limb-onset distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal/Left-sided colorectal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Distal/Left-sided colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Distal colorectal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Distal colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PMC8104016-hcg-12-e002353-s006.xlsx-mTHP-1-LPS_Prom-Distal-RefSeq_Name_IRF6 Gene SetFrom Rummagene Transcription Factor Associations 2026 target genes of the PMC8104016-hcg-12-e002353-s006.xlsx-mTHP-1-LPS_Prom-Distal-RefSeq_Name_IRF6 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset. |
Focal dermal hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Focal dermal hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and presenile cataract syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Fibular hypoplasia and complex brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Tibia, hypoplasia of, with polydactyly Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Tibia, hypoplasia of, with polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital adrenal hypoplasia, X-linked Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Foveal hypoplasia and anterior segment dysgenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia, type 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 2D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Optic nerve hypoplasia, bilateral Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Optic nerve hypoplasia, bilateral phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Splenic hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Splenic hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Olivopontocerebellar hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Olivopontocerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia, type 1b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 1b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 2B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia, type 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia type 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pontocerebellar hypoplasia, type 2e Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pontocerebellar hypoplasia, type 2e phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skeletal defects, genital hypoplasia, and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Focal Dermal Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Focal Dermal Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Fibular hypoplasia and complex brachydactyly Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Fibular hypoplasia and complex brachydactyly from the curated CTD Gene-Disease Associations dataset. |
Cartilage-hair hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cartilage-hair hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Leydig Cell Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Leydig Cell Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Optic Nerve Hypoplasia, Bilateral Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Optic Nerve Hypoplasia, Bilateral from the curated CTD Gene-Disease Associations dataset. |
Polymicrogyria With Optic Nerve Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polymicrogyria With Optic Nerve Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 2C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2C from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 2B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2B from the curated CTD Gene-Disease Associations dataset. |
ADRENAL HYPOPLASIA, CONGENITAL Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ADRENAL HYPOPLASIA, CONGENITAL from the curated CTD Gene-Disease Associations dataset. |
Anophthalmia with pulmonary hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Anophthalmia with pulmonary hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 6 from the curated CTD Gene-Disease Associations dataset. |
PONTOCEREBELLAR HYPOPLASIA, TYPE 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease PONTOCEREBELLAR HYPOPLASIA, TYPE 4 from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 1 from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 3 from the curated CTD Gene-Disease Associations dataset. |
Iris hypoplasia and glaucoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset. |
Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset. |
Pontocerebellar Hypoplasia Type 2A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pontocerebellar Hypoplasia Type 2A from the curated CTD Gene-Disease Associations dataset. |
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset. |
Foveal Hypoplasia and Anterior Segment Dysgenesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Foveal Hypoplasia and Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset. |
focal dermal hypoplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease focal dermal hypoplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
dental enamel hypoplasia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease dental enamel hypoplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
focal dermal hypoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease focal dermal hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cartilage-hair hypoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cartilage-hair hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pituitary hypoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pituitary hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
dental enamel hypoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease dental enamel hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cleft lip; cleft palate; dental enamel hypoplasia; enamel, hypoplastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypoplasia Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term hypoplasia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
retinal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the retinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of choroid Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of choroid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |