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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 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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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 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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
hypoplasia of proximal fibula Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of proximal fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of proximal radius Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of proximal radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Proximal Tibial Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Tibial Hypoplasia 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 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 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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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 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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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. |
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, proximal, 1b Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Symphalangism, proximal, 1b phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset. |
vulvar proximal-type epithelioid sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vulvar proximal-type epithelioid sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
H3K4me3_epithelial cell of proximal tubule_hg19_2 Gene SetFrom ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_epithelial cell of proximal tubule_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset. |
H3K4me3_epithelial cell of proximal tubule_hg19_1 Gene SetFrom ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_epithelial cell of proximal tubule_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset. |
CTCF_epithelial cell of proximal tubule_hg19_1 Gene SetFrom ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_epithelial cell of proximal tubule_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset. |
CTCF_epithelial cell of proximal tubule_hg19_2 Gene SetFrom ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_epithelial cell of proximal tubule_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles 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. |
fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
proximal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term proximal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
LMX1B_KO_GDS3320_57_mouse_embryonic (e11.5) proximal hindlimb bud tissues Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LMX1B_KO_GDS3320_57_mouse_embryonic (e11.5) proximal hindlimb bud tissues gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations 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. |
proximal convoluted tubule segment 2 development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal convoluted tubule segment 2 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. |
proximal tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric proximal convoluted tubule segment 2 development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric proximal convoluted tubule segment 2 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 straight tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal straight tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric proximal tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric proximal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric proximal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric proximal convoluted tubule development 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. |
proximal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric proximal straight tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric proximal straight tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
core promoter proximal region dna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the core promoter proximal region dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii core promoter proximal region 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 core promoter proximal region 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 core promoter proximal region sequence-specific dna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii core promoter proximal region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii core promoter proximal region 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 core promoter proximal region sequence-specific dna binding transcription factor activity involved in negative regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
core promoter proximal region sequence-specific dna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the core promoter proximal region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
proximal tapering of metacarpals Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal tapering of metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small proximal tibial epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the small proximal tibial epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphyses of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short metacarpals with rounded proximal ends Gene SetFrom HPO Gene-Disease Associations genes associated with the short metacarpals with rounded proximal ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
club-shaped proximal femur Gene SetFrom HPO Gene-Disease Associations genes associated with the club-shaped proximal femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal tibial epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal tibial epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
late-onset proximal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the late-onset proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal fibular overgrowth Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal fibular overgrowth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multicentric ossification of proximal femoral epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the multicentric ossification of proximal femoral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multicentric ossification of proximal humeral epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the multicentric ossification of proximal humeral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal renal tubular acidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
widened proximal tibial metaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the widened proximal tibial metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shortening of all proximal phalanges of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the shortening of all proximal phalanges of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphyses of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal tibial hypopolasia Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal tibial hypopolasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pointed proximal second through fifth metacarpals Gene SetFrom HPO Gene-Disease Associations genes associated with the pointed proximal second through fifth metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
limited mobility of proximal interphalangeal joint Gene SetFrom HPO Gene-Disease Associations genes associated with the limited mobility of proximal interphalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent proximal finger flexion creases Gene SetFrom HPO Gene-Disease Associations genes associated with the absent proximal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal femoral epiphysiolysis Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal femoral epiphysiolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
non-acidotic proximal tubulopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the non-acidotic proximal tubulopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal/middle symphalangism of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
stippled calcification proximal humeral epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the stippled calcification proximal humeral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal femoral metaphyseal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tombstone-shaped proximal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the tombstone-shaped proximal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal symphalangism Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal symphalangism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal upper limb amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symphalangism affecting the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the symphalangism affecting the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mottled pigmentation of the trunk and proximal extremities Gene SetFrom HPO Gene-Disease Associations genes associated with the mottled pigmentation of the trunk and proximal extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal muscle weakness in lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal muscle weakness in lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal radio-ulnar synostosis Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal radio-ulnar synostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
metaphyseal cupping of proximal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the metaphyseal cupping of proximal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive proximal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
irregular proximal tibial epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the irregular proximal tibial epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal femoral metaphyseal irregularity Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal femoral metaphyseal irregularity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal tubulopathy Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal tubulopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
swelling of proximal interphalangeal joints Gene SetFrom HPO Gene-Disease Associations genes associated with the swelling of proximal interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cone-shaped epiphyses of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the cone-shaped epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thin proximal phalanges with broad epiphyses of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the thin proximal phalanges with broad epiphyses of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
contracture of the proximal interphalangeal joint of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the contracture of the proximal interphalangeal joint of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal muscle weakness in upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal muscle weakness in upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlargement of the proximal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the enlargement of the proximal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal lower limb amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged proximal interphalangeal joints Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged proximal interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pseudoepiphyses of the proximal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the pseudoepiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal symphalangism (hands) Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal symphalangism (hands) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dilated proximal convoluted tubules Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated proximal convoluted tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent proximal rib Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent proximal rib phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
proximal convoluted tubule brush border loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the proximal convoluted tubule brush border loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal proximal convoluted tubule brush border morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal proximal convoluted tubule brush border 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. |
abnormal proximal convoluted tubule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal proximal convoluted tubule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent proximal convoluted tubule brush border Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent proximal convoluted tubule brush border phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
symphalangism, proximal, 1b Gene SetFrom OMIM Gene-Disease Associations genes associated with the symphalangism, proximal, 1b phenotype from the curated OMIM Gene-Disease Associations dataset. |
symphalangism, proximal Gene SetFrom OMIM Gene-Disease Associations genes associated with the symphalangism, proximal phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, proximal, with early respiratory muscle involvement Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, proximal, with early respiratory muscle involvement phenotype from the curated OMIM Gene-Disease Associations dataset. |
hereditary motor and sensory neuropathy, proximal type Gene SetFrom OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy, proximal type phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal tubular acidosis, proximal, with ocular abnormalities Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, proximal, with ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal proximal tubule Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue renal proximal tubule from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
renal proximal tubule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue renal proximal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
proximal deep inguinal lymph node Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue proximal deep inguinal lymph node in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Dissection Of Proximal Aorta Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dissection Of Proximal Aorta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hmn (Hereditary Motor Neuropathy) Proximal Type I Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hmn (Hereditary Motor Neuropathy) Proximal Type I in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Asymmetric Diabetic Proximal Motor Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Asymmetric Diabetic Proximal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Symmetric Diabetic Proximal Motor Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Symmetric Diabetic Proximal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal-Type Epithelioid Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal-Type Epithelioid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Myopathy With Focal Depletion Of Mitochondria Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy With Focal Depletion Of Mitochondria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Symphalangism Of Hands Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Symphalangism Of Hands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Femoral Metaphyseal Abnormality Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Femoral Metaphyseal Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Irregular Proximal Tibial Epiphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Irregular Proximal Tibial Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Small Proximal Tibial Epiphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Small Proximal Tibial Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Shortening Of All Proximal Phalanges Of The Fingers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Shortening Of All Proximal Phalanges Of The Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thin Proximal Phalanges With Broad Epiphyses Of The Hand Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thin Proximal Phalanges With Broad Epiphyses Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Non-Acidotic Proximal Tubulopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Non-Acidotic Proximal Tubulopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Proximal Myelopathic Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Proximal Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Proximal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatiguable Weakness Of Proximal Limb Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatiguable Weakness Of Proximal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Flexion Contracture Of Proximal Interphalangeal Joint Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flexion Contracture Of Proximal Interphalangeal Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Metacarpals With Rounded Proximal Ends Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Metacarpals With Rounded Proximal Ends in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Tubulopathy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Tubulopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Muscle Weakness In Lower Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness In Lower Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Muscle Weakness In Upper Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness In Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Delayed Proximal Femoral Epiphyseal Ossification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Proximal Femoral Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal/Middle Symphalangism Of 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal/Middle Symphalangism Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Widened Proximal Tibial Metaphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widened Proximal Tibial Metaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Late-Onset Proximal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Fibular Overgrowth Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Fibular Overgrowth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Lower Limb Amyotrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Lower Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Enlargement Of The Proximal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlargement Of The Proximal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Proximal Finger Flexion Creases Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Proximal Finger Flexion Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Femoral Metaphyseal Irregularity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Femoral Metaphyseal Irregularity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Radio-Ulnar Synostosis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Radio-Ulnar Synostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Metaphyseal Cupping Of Proximal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Metaphyseal Cupping Of Proximal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Club-Shaped Proximal Femur Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Club-Shaped Proximal Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multicentric Ossification Of Proximal Femoral Epiphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Ossification Of Proximal Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multicentric Ossification Of Proximal Humeral Epiphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Ossification Of Proximal Humeral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Upper Limb Amyotrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tombstone-Shaped Proximal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tombstone-Shaped Proximal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pointed Proximal Second Through Fifth Metacarpals Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pointed Proximal Second Through Fifth Metacarpals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Tibial And Fibular Fusion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Tibial And Fibular Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Stippled Calcification Proximal Humeral Epiphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Stippled Calcification Proximal Humeral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Tapering Of Metacarpals Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Tapering Of Metacarpals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Enlarged Proximal Interphalangeal Joints Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlarged Proximal Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Mottled Pigmentation Of The Trunk And Proximal Extremities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mottled Pigmentation Of The Trunk And Proximal Extremities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Upper Limb Muscle Hypertrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Upper Limb Muscle Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Swelling Of Proximal Interphalangeal Joints Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Swelling Of Proximal Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Wide Proximal Femoral Metaphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Proximal Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Limited Mobility Of Proximal Interphalangeal Joint Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Mobility Of Proximal Interphalangeal Joint 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 proximal tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric proximal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
proximal tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the proximal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
proximal dendrite Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the proximal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
proximal neuron projection Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the proximal neuron projection cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
abnormal proximal convoluted tubule morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal proximal convoluted tubule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent proximal convoluted tubule brush border Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent proximal convoluted tubule brush border phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent proximal rib Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent proximal rib phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated proximal convoluted tubule Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated proximal convoluted tubule 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. |
proximal convoluted tubule brush border loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the proximal convoluted tubule brush border loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal proximal convoluted tubule brush border morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal proximal convoluted tubule brush border morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Lung v1 - L2 - Proximal Basal Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L2 - Proximal Basal cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Lung v1 - L2 - Proximal Ciliated Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L2 - Proximal Ciliated cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L1 - Proximal Tubule Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L1 - Proximal Tubule cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Proximal Tubule Epithelial Segment 1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Proximal Tubule Epithelial Segment 1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Proximal Tubule Epithelial Segment 2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Proximal Tubule Epithelial Segment 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Proximal Tubule Epithelial Segment 3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Proximal Tubule Epithelial Segment 3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Proximal Tubule Epithelial Segment 1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Proximal Tubule Epithelial Segment 1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Proximal Tubule Epithelial Segment 2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Proximal Tubule Epithelial Segment 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Proximal Tubule Epithelial Segment 3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Proximal Tubule Epithelial Segment 3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Proximal limb bone cell_Bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal limb bone cell_Bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal limb bud cell_Limb bud_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal limb bud cell_Limb bud_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Enterocyte proximal cell_Intestine_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Enterocyte proximal cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal stem cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal stem cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal tubular cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal tubule cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal tubule cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Early proximal tubule cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Early proximal tubule cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal segment cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal segment cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
General proximal cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the General proximal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
S3 proximal cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the S3 proximal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
S2 proximal cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the S2 proximal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
S1 proximal cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the S1 proximal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal tubular cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal tubule (PT) cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal tubule (PT) cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal straight tubular cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal straight tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal convoluted tubular cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal convoluted tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal tubule cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal tubule cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal convoluted tubular cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal convoluted tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal straight tubular cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal straight tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal tubule-S1 cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal tubule-S1 cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
S3 proximal tubule cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the S3 proximal tubule cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
S1/S2 proximal tubule cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the S1/S2 proximal tubule cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal cell_Blood vessel_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal cell_Blood vessel_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal tubular cell_Liver_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal tubular cell_Liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal epithelial cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal epithelial cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal cell_Prostate_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal cell_Prostate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal luminal cell_Prostate_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal luminal cell_Prostate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal S2 cell_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal S2 cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal tubular cell_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal tubular cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal S3 cell_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal S3 cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Proximal tubular cell_Urine_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Proximal tubular cell_Urine_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Regucalcin in proximal tubule epithelial kidney cells Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Regucalcin in proximal tubule epithelial kidney cells pathway from the WikiPathways Pathways 2024 dataset. |
Proximal tubule transport Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Proximal tubule transport pathway from the WikiPathways Pathways 2024 dataset. |
16p11 2 proximal deletion syndrome Gene SetFrom WikiPathways Pathways 2024 proteins participating in the 16p11 2 proximal deletion syndrome pathway from the WikiPathways Pathways 2024 dataset. |
Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) Gene Setproteins participating in the Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) 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 proximal tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric proximal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
proximal tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the proximal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
proximal dendrite Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the proximal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
proximal neuron projection Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the proximal neuron projection cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Proximal symphalangism Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Proximal symphalangism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Vulvar proximal-type epithelioid sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vulvar proximal-type epithelioid sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant adult-onset proximal spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant adult-onset proximal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Renal proximal tubule Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Renal proximal tubule from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Renal proximal tubule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal proximal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Renal proximal tubule cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal proximal tubule cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Renal proximal tubule epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal proximal tubule epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Renal proximal tubule epithelial cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal proximal tubule epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Renal proximal tubule epithelium cell line Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal proximal tubule epithelium cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Proximal deep inguinal lymph node Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Proximal deep inguinal lymph node in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Proximal portion of axoneme Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proximal portion of axoneme cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Proximal dendrite Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proximal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Proximal neuron projection Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proximal neuron projection cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Proximal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Proximal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Proximal portion of axoneme Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Proximal portion of axoneme cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor proximal connecting cilium Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Photoreceptor proximal connecting cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Apical proximal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Apical proximal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Basal proximal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Basal proximal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Adult-onset proximal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive proximal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal symphalangism Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal symphalangism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant childhood-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Gastric adenocarcinoma and proximal polyposis of the stomach Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Gastric adenocarcinoma and proximal polyposis of the stomach phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal lower limb amyotrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal lower limb amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal muscle weakness in lower limbs Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal muscle weakness in lower limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive proximal renal tubular acidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive proximal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal amyotrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal colorectal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Proximal colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Proximal tubule bicarbonate reclamation Gene SetFrom KEGG Pathways 2026 proteins participating in the Proximal tubule bicarbonate reclamation pathway from the KEGG Pathways 2026 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. |
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 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. |
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. |
hypoplasia of lymphatic vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
parathyroid hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the parathyroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pancreatic hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pancreatic hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ventral pons Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ventral pons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
glenoid fossa hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the glenoid fossa hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lymph node hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the lymph node hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
posterior vertebral hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the posterior vertebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the lacrimal puncta Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the lacrimal puncta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the nasal bone Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of penis Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of penis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
optic disc hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the optic disc hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the thymus Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thyroid hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the thyroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the odontoid process Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
calf muscle hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the calf muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
erythroid hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the erythroid hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the pons Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the pons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
breast hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the breast hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ciliary body Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ciliary body phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the corpus callosum Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the brainstem Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the bladder Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the pharynx Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the pharynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
macular hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the macular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pectoralis hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pectoralis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
midclavicular hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the midclavicular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
mandibular condyle hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the mandibular condyle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
corticospinal tract hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the corticospinal tract hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
carpal bone hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the carpal bone hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations 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. |
hypoplasia of the calcaneus Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the calcaneus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of deltoid muscle Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of deltoid muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the renal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the uterus Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the uterus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
laryngeal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the laryngeal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lacrimal gland hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the lacrimal gland hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
frontal bone hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the frontal bone hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
unilateral breast hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the unilateral breast hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thoracic hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the thoracic hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pectoralis major hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pectoralis major hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adrenal medullary hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the adrenal medullary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
labial hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the labial hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the maxilla Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the maxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
inferior vermis hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the inferior vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the semicircular canal Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the semicircular canal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ear cartilage Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ear cartilage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
external genital hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the external genital hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the vagina Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the vagina phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of first ribs Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of first ribs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar hemisphere hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar hemisphere hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
gonadal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the gonadal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the iris Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the iris phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
2nd-5th toe middle phalangeal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the 2nd-5th toe middle phalangeal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebellar vermis hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebellar vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adrenocortical hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the adrenocortical hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the ovary Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the ovary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized cerebral atrophy/hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized cerebral atrophy/hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the prostate Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the prostate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the lesser trochanter Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the lesser trochanter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
unilateral chest hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the unilateral chest hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
vertebral hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the vertebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shoulder muscle hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the shoulder muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the pyramidal tract Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the pyramidal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cerebral hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the cerebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the cochlea Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the fovea Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the fovea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
optic nerve hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the optic nerve hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
adrenal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the adrenal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hemifacial hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the hemifacial hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of dental enamel Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of dental enamel phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anterior pituitary hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the anterior pituitary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the frontal lobes Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the frontal lobes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
scrotal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the scrotal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
intestinal hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the intestinal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the fallopian tube Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper limb muscle hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
patellar hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the patellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the epiglottis Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the epiglottis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fibular hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the fibular hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pulmonary artery hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the pulmonary artery hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the abdominal wall musculature Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
paranasal sinus hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the paranasal sinus hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
clitoral hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the clitoral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
olivopontocerebellar hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the olivopontocerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
axillary apocrine gland hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the axillary apocrine gland hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Dental Enamel Hypoplasia Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Dental Enamel Hypoplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
testis hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the testis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
tongue hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the tongue hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
genital tubercle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the genital tubercle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
lymphoid hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the lymphoid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
palatine bone horizontal plate hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the palatine bone horizontal plate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thyroid hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thyroid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hindbrain hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hindbrain hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
midface hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the midface hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
intervertebral disk hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the intervertebral disk hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
lymph node hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the lymph node hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aortic arch hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aortic arch hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pituitary intermediate lobe hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pituitary intermediate lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
temporal bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the temporal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
iris stroma hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the iris stroma hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ischium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ischium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
oviduct hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the oviduct hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
spleen hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the spleen hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
radius hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the radius hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
otic vesicle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the otic vesicle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
malleus hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the malleus hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
maxilla hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the maxilla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
uterine cervix hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the uterine cervix hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
adrenal gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the adrenal gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
palatal shelf hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the palatal shelf hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ventricle myocardium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ventricle myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
leydig cell hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the leydig cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
mammary gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the mammary gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
scrotum hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the scrotum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
diencephalon hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the diencephalon hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cochlear ganglion hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cochlear ganglion hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
frontal bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the frontal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
head mesenchyme hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the head mesenchyme hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
myometrium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the myometrium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
papillary muscle hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the papillary muscle hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cerebellum vermis hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cerebellum vermis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
sebaceous gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the sebaceous gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
premaxilla hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the premaxilla hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
atrium myocardium hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the atrium myocardium hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pulmonary hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pulmonary hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
female preputial gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the female preputial gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pharyngeal arch artery hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pharyngeal arch artery hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
epididymis hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the epididymis hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
parathyroid hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the parathyroid hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
olfactory bulb hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the olfactory bulb hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
aorta hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the aorta hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
heart hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the heart hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ethmoturbinate hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ethmoturbinate hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hyoid bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hyoid bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pituitary gland hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pituitary gland hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
parietal bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the parietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
axial mesoderm hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the axial mesoderm hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
mesangial cell hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the mesangial cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
liver hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the liver hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
palatine bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the palatine bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
pancreas hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the pancreas hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
gonial bone hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the gonial bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ear lobe hypoplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ear lobe hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |