Complete duplication of thumb phalanx

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Results for "Complete duplication of thumb phalanx": 17 genes, 403 gene sets

Name
DUP5P13 Gene Chromosome 5p13 duplication* syndrome*
CXDUPQ26.3 Gene Chromosome Xq26.3 duplication* syndrome*
OPHLC Gene Omphalocele due to duplication* of 1p31.3*
DUP16P11.2 Gene Chromosome 16p11.2 duplication* syndrome*
DUP17Q23.1Q23.2 Gene Chromosome 17q23.1-q23.2 duplication* syndrome*
DUP2Q31.1 Gene Chromosome 2q31.1 duplication* syndrome*
DUP16P13.3 Gene Chromosome 16p13.3 duplication* syndrome*
DUPXQ28 Gene Chromosome Xq28 duplication* syndrome*
DUP7Q11.23 Gene Chromosome 7q11.23 duplication* syndrome*
DUPXQ27.3Q28 Gene Chromosome Xq27.3-q28 duplication* syndrome*
DUP17P13.3 Gene Chromosome 17p13.3 duplication* syndrome*
DUP17Q12 Gene Chromosome 17q12 duplication* syndrome*
DUPXP11.23P11.22 Gene Chromosome Xp11.23-p11.22 duplication* syndrome*
DUP1Q21 Gene Chromosome 1q21.1 duplication* syndrome*
DUP17Q21.31 Gene Chromosome 17q21.31 duplication* syndrome*
DUP8Q22.1 Gene Leri pleonosteosis chromosome duplication* syndrome*
DUP22Q13 Gene Chromosome 22q13 duplication* syndrome*
complete duplication of thumb phalanx Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Complete Duplication Of Thumb Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Duplication Of Thumb Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
complete duplication of proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Complete Duplication Of Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Duplication Of Proximal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of Proximal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
duplication of the proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of thumb phalanx Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of thumb phalanx Gene Set From HPO Gene-Disease Associations genes associated with the duplication of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Duplication Of Thumb Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duplication Of Thumb Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Duplication Of Thumb Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of Thumb Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
complete duplication of phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Complete Duplication Of The Middle Phalanx Of The 3Rd Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Duplication Of The Middle Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Complete Duplication Of Hallux Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Duplication Of Hallux Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormality of thumb phalanx Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the broad distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
radial deviation of thumb terminal phalanx Gene Set From HPO Gene-Disease Associations genes associated with the radial deviation of thumb terminal phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bifid distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the bifid distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the short phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent proximal phalanx of thumb Gene Set From HPO Gene-Disease Associations genes associated with the absent proximal phalanx of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short proximal phalanx of thumb Gene Set From HPO Gene-Disease Associations genes associated with the short proximal phalanx of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Radial Deviation Of Thumb Terminal Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Radial Deviation Of Thumb Terminal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bifid Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bifid Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Proximal Phalanx Of Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Proximal Phalanx Of Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Proximal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Proximal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Triangular shaped proximal phalanx of the thumb Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Triangular shaped proximal phalanx of the thumb phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
complete duplication of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of the middle phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Complete Duplication Of The Distal Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
duplication of phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of distal phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the duplication of distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of middle phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the duplication of middle phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of phalanx of 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of phalanx of 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the middle phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the middle phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the proximal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of phalanx of hallux Gene Set From HPO Gene-Disease Associations genes associated with the duplication of phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Partial Duplication Of The Distal Phalanx Of The 2Nd Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Duplication Of The Distal Phalanx Of The 3Rd Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duplication Of The Proximal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duplication Of The Proximal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Duplication Of The Distal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Duplication Of The Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Duplication Of Phalanx Of Hallux Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duplication Of Phalanx Of Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Duplication Of The Distal Phalanx Of Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duplication Of The Distal Phalanx Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Stapes ankylosis with broad thumb and toes Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From HPO Gene-Disease Associations genes associated with the flexion contracture of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal placement of thumb Gene Set From 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.
dysplastic distal thumb phalanges with a central hole Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
aplasia/hypoplasia of the phalanges of the thumb Gene Set From 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.
short thumb Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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.
aplasia/hypoplasia of the thumb Gene Set From 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.
DNA polymerase beta, thumb domain Gene Set From 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 Set From 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 Set From 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 Set From OMIM Gene-Disease Associations genes associated with the triphalangeal thumb, type i phenotype from the curated OMIM Gene-Disease Associations dataset.
Triphalangeal Thumb Gene Set From 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 Set From 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 Set From 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.
Thumb Aplasia Gene Set From 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.
Stapes Ankylosis With Broad Thumb And Toes (Disorder) Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Adducted Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Placement Of Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Placement Of Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Thumb Deformity Gene Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From 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 Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Thumb osteoarthritis severity (hand Klsum) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
46,XY gonadal dysgenesis, complete, dhh-related Gene Set From ClinVar Gene-Phenotype Associations genes associated with the 46,XY gonadal dysgenesis, complete, dhh-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease 46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related from the curated CTD Gene-Disease Associations dataset.
complete hearing loss; deafness; vestibular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; vestibular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complete hearing loss; deafness; hearing loss, bilateral Gene Set From GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; hearing loss, bilateral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complete hearing loss; deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complete androgen insensitivity syndrome and sertoli cell adenoma Gene Set From GAD Gene-Disease Associations genes associated with the disease complete androgen insensitivity syndrome and sertoli cell adenoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene Set From GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complete hearing loss; deafness; hearing loss, sensorineural; sensorineural hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complete hearing loss; deafness; hearing impairment; hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; hearing impairment; hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complete androgen insensitivity Gene Set From GAD Gene-Disease Associations genes associated with the disease complete androgen insensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complete hearing loss; deafness; hearing loss, bilateral; hearing loss, sensorineural; sensorineural hearing loss Gene Set From GAD Gene-Disease Associations genes associated with the disease complete hearing loss; deafness; hearing loss, bilateral; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
complete Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term complete in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
complete heart block with broad rs complexes Gene Set From HPO Gene-Disease Associations genes associated with the complete heart block with broad rs complexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
1-5 finger complete cutaneous syndactyly Gene Set From HPO Gene-Disease Associations genes associated with the 1-5 finger complete cutaneous syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete atrioventricular canal defect Gene Set From HPO Gene-Disease Associations genes associated with the complete atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic) Gene Set From HPO Gene-Disease Associations genes associated with the nearly complete absence of metabolically active adipose tissue (subcutaneous, intraabdominal, intrathoracic) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete lethality during fetal growth through weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete lethality during fetal growth through weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete embryonic lethality at implantation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete embryonic lethality at implantation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete embryonic lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete embryonic lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete embryonic lethality between implantation and placentation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete embryonic lethality between implantation and placentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete preweaning lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete preweaning lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete embryonic lethality before implantation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete embryonic lethality before implantation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete embryonic lethality between somite formation and embryo turning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete embryonic lethality between somite formation and embryo turning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete perinatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete perinatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete lethality at weaning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete lethality at weaning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete embryonic lethality between implantation and somite formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete embryonic lethality between implantation and somite formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete neonatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete neonatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete lethality throughout fetal growth and development Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete lethality throughout fetal growth and development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
unbalanced complete common atrioventricular canal Gene Set From MPO Gene-Phenotype Associations gene mutations causing the unbalanced complete common atrioventricular canal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete prenatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete prenatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete atrioventricular septal defect Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete embryonic lethality during organogenesis Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete embryonic lethality during organogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
complete postnatal lethality Gene Set From MPO Gene-Phenotype Associations gene mutations causing the complete postnatal lethality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
night blindness, congenital stationary (complete), 1f, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the night blindness, congenital stationary (complete), 1f, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
night blindness, congenital stationary (complete), 1b, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the night blindness, congenital stationary (complete), 1b, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
night blindness, congenital stationary (complete), 1c, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the night blindness, congenital stationary (complete), 1c, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
night blindness, congenital stationary (complete), 1a, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the night blindness, congenital stationary (complete), 1a, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
night blindness, congenital stationary (complete), 1e, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the night blindness, congenital stationary (complete), 1e, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
adrenal insufficiency, congenital, with 46xy sex reversal, partial or complete Gene Set From OMIM Gene-Disease Associations genes associated with the adrenal insufficiency, congenital, with 46xy sex reversal, partial or complete phenotype from the curated OMIM Gene-Disease Associations dataset.
night blindness, congenital stationary (complete), 1d, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the night blindness, congenital stationary (complete), 1d, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
Complete Trisomy 21 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Trisomy 21 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Atrioventricular Block Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Atrioventricular Block in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Trisomy 18 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Trisomy 18 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Argininosuccinic Acid Synthetase Deficiency, Complete Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Argininosuccinic Acid Synthetase Deficiency, Complete in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Hydatidiform Mole Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Hydatidiform Mole in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Congenital Stationary Night Blindness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Congenital Stationary Night Blindness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Paraplegia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Paraplegia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal, Partial Or Complete Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal, Partial Or Complete in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Or Complete Agenesis Of Corpus Callosum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Or Complete Agenesis Of Corpus Callosum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
46,Xy Gonadal Dysgenesis, Complete Or Partial, Dhh-Related Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 46,Xy Gonadal Dysgenesis, Complete Or Partial, Dhh-Related in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Heart Block With Broad Qrs Complexes Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Heart Block With Broad Qrs Complexes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
46,Xy Gonadal Dysgenesis, Complete, Sry-Related Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease 46,Xy Gonadal Dysgenesis, Complete, Sry-Related in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Hearing Loss Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Hearing Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Electrocardiogram Atrioventricular Block Complete Heart Block Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Electrocardiogram Atrioventricular Block Complete Heart Block in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Complete Right Bundle Branch Block Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Right Bundle Branch Block in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Complete Spermatogenic Arrest Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Spermatogenic Arrest in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Complete Breech Presentation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Breech Presentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
embryonic lethality during organogenesis, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality during organogenesis, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality between somite formation and embryo turning, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality between somite formation and embryo turning, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
postnatal lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the postnatal lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
perinatal lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the perinatal lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neonatal lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neonatal lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
prenatal lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the prenatal lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality throughout fetal growth and development, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality throughout fetal growth and development, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality between implantation and somite formation, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality between implantation and somite formation, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality between implantation and placentation, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality between implantation and placentation, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality at weaning, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality at weaning, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality before implantation, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality before implantation, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality at implantation, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality at implantation, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
complete atrioventricular septal defect Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
preweaning lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the preweaning lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality during fetal growth through weaning, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality during fetal growth through weaning, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
complete cleft palate Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the complete cleft palate phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
lethality, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the lethality, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
balanced complete atrioventricular canal Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the balanced complete atrioventricular canal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
unbalanced complete atrioventricular canal, left dominant Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the unbalanced complete atrioventricular canal, left dominant phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
unbalanced complete common atrioventricular canal Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the unbalanced complete common atrioventricular canal phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality prior to organogenesis, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality prior to organogenesis, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic lethality prior to tooth bud stage, complete penetrance Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic lethality prior to tooth bud stage, complete penetrance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
preweaning lethality, complete penetrance Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the preweaning lethality, complete penetrance phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
Complete generalized lipodystrophy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Complete generalized lipodystrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Complete androgen insensitivity syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complete androgen insensitivity syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Complete generalized lipodystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Complete generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Methylmalonic aciduria due to complete methylmalonyl-CoA mutase deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Methylmalonic aciduria due to complete methylmalonyl-CoA mutase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atypical severe combined immunodeficiency due to complete RAG1/2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Complete remission in asthma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Complete remission in asthma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Caudal Duplication Anomaly Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Caudal Duplication Anomaly from the curated CTD Gene-Disease Associations dataset.
Williams-Beuren Region Duplication Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Williams-Beuren Region Duplication Syndrome from the curated CTD Gene-Disease Associations dataset.
duplication Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term duplication in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
centrosome duplication Gene Set From GO Biological Process Annotations 2015 genes participating in the centrosome duplication biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2015 dataset.
regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2015 dataset.
fibular duplication Gene Set From HPO Gene-Disease Associations genes associated with the fibular duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the phalanges of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
renal duplication Gene Set From HPO Gene-Disease Associations genes associated with the renal duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of bones involving the upper extremities Gene Set From HPO Gene-Disease Associations genes associated with the duplication of bones involving the upper extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ureteral duplication Gene Set From HPO Gene-Disease Associations genes associated with the ureteral duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the phalanges of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the phalanges of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the phalanges of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of renal pelvis Gene Set From HPO Gene-Disease Associations genes associated with the duplication of renal pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of hand bones Gene Set From HPO Gene-Disease Associations genes associated with the duplication of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of internal organs Gene Set From HPO Gene-Disease Associations genes associated with the duplication of internal organs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb duplication Gene Set From HPO Gene-Disease Associations genes associated with the limb duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal urethral duplication Gene Set From HPO Gene-Disease Associations genes associated with the distal urethral duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication involving bones of the feet Gene Set From HPO Gene-Disease Associations genes associated with the duplication involving bones of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Chromosome Duplication Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Chromosome Duplication phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Friend of PRMT1 duplication Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Friend of PRMT1 duplication protein domain from the InterPro Predicted Protein Domain Annotations dataset.
rostral-caudal axis duplication Gene Set From MPO Gene-Phenotype Associations gene mutations causing the rostral-caudal axis duplication phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
chromosome 17q21.31 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q21.31 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xp11.23-p11.22 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xp11.23-p11.22 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
leri pleonosteosis chromosome duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the leri pleonosteosis chromosome duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 7q11.23 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 7q11.23 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
?caudal duplication anomaly Gene Set From OMIM Gene-Disease Associations genes associated with the ?caudal duplication anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.
omphalocele due to duplication of 1p31.3 Gene Set From OMIM Gene-Disease Associations genes associated with the omphalocele due to duplication of 1p31.3 phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 1q21.1 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 1q21.1 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xq28 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xq28 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17q23.1-q23.2 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q23.1-q23.2 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 22q13 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 22q13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16p11.2 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16p11.2 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 16p13.3 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 16p13.3 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome xq27.3-q28 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome xq27.3-q28 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17p13.3 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17p13.3 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 2q31.1 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 2q31.1 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
split-hand/foot malformation 3, gene duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the split-hand/foot malformation 3, gene duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 17q12 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 17q12 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 19p13.13 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 19p13.13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 5p13 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 5p13 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
Chromosome Xq26.3 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Xq26.3 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 11Q Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 11Q Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Caudal Duplication Anomaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Caudal Duplication Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Duplication Of Uterus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Duplication Of Uterus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Duplication Of Intestine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Duplication Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome Xq27.3-Q28 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Xq27.3-Q28 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Urethral Duplication Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Urethral Duplication in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome Xp11.23-P11.22 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome Xp11.23-P11.22 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 5P13 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 5P13 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duplication Of Internal Organs Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duplication Of Internal Organs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17P13.3 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17P13.3 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Xq25 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Xq25 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 17Q23.1-Q23.2 Duplication Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 17Q23.1-Q23.2 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duplication 15Q11-Q13 Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duplication 15Q11-Q13 Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duplication Of Renal Pelvis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duplication Of Renal Pelvis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fibular Duplication Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fibular Duplication in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Chromosome Xq28 Duplication Syndrome Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Chromosome Xq28 Duplication Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2023 genes participating in the regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2023 dataset.
negative regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2023 genes participating in the negative regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2023 dataset.
rostral-caudal axis duplication Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the rostral-caudal axis duplication phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
duplication of ductus venosus Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the duplication of ductus venosus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2025 genes participating in the regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2025 dataset.
negative regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2025 genes participating in the negative regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2025 dataset.
positive regulation of centrosome duplication Gene Set From GO Biological Process Annotations 2025 genes participating in the positive regulation of centrosome duplication biological process from the curated GO Biological Process Annotations 2025 dataset.
Chromosomal duplication syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Chromosomal duplication syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
7q11.23 duplication syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease 7q11.23 duplication syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Chromosomal duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosomal duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17p13.3 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17p13.3 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
7q11.23 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease 7q11.23 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome Xp11.22 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome Xp11.22 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 16p11.2 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 16p11.2 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 1q21.1 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 1q21.1 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17q21.31 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17q21.31 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Gene duplication disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Gene duplication disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 17q12 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 17q12 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 16p13.3 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 16p13.3 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 22q13 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 22q13 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Central nervous system tumor with BCOR internal tandem duplication Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Central nervous system tumor with BCOR internal tandem duplication in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 5p13 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 5p13 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Intestinal duplication Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Intestinal duplication phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Caudal duplication Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Caudal duplication phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
abnormality of phalanx of finger Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
sclerosis of finger phalanx Gene Set From GWASdb SNP-Phenotype Associations genes associated with the sclerosis of finger phalanx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of the middle phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad phalanx of the toes Gene Set From HPO Gene-Disease Associations genes associated with the broad phalanx of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symphalangism of middle phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the symphalangism of middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bracket epiphysis of the middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the bracket epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged epiphysis of the proximal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent middle phalanx of 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the absent middle phalanx of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
patchy sclerosis of finger phalanx Gene Set From HPO Gene-Disease Associations genes associated with the patchy sclerosis of finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the middle phalanx of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the middle phalanx of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped middle phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphyses of the distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slender proximal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the slender proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular epiphysis of the middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped proximal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped middle phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphysis of the middle phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sclerosis of distal finger phalanx Gene Set From HPO Gene-Disease Associations genes associated with the sclerosis of distal finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symphalangism of middle phalanx of 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the symphalangism of middle phalanx of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
long proximal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the long proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad hallux phalanx Gene Set From HPO Gene-Disease Associations genes associated with the broad hallux phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad middle phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the broad middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short middle phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the short middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypersegmentation of proximal phalanx of second finger Gene Set From HPO Gene-Disease Associations genes associated with the hypersegmentation of proximal phalanx of second finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
long phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the long phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slender distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the slender distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the broad distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short middle phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the short middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short proximal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the short proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad distal phalanx of the toes Gene Set From HPO Gene-Disease Associations genes associated with the broad distal phalanx of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular epiphysis of the proximal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad distal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the broad distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular epiphysis of the proximal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bracket epiphysis of the middle phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the bracket epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphysis of the proximal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged epiphysis of the middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the short middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fifth finger distal phalanx clinodactyly Gene Set From HPO Gene-Disease Associations genes associated with the fifth finger distal phalanx clinodactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the short phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short proximal phalanx of hallux Gene Set From HPO Gene-Disease Associations genes associated with the short proximal phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
long distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the long distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short phalanx of hallux Gene Set From HPO Gene-Disease Associations genes associated with the short phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bifid distal phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the bifid distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symphalangism affecting the proximal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the symphalangism affecting the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphysis of the middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped proximal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypersegmentation of proximal phalanx of third finger Gene Set From HPO Gene-Disease Associations genes associated with the hypersegmentation of proximal phalanx of third finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged epiphysis of the proximal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sclerosis of finger phalanx Gene Set From HPO Gene-Disease Associations genes associated with the sclerosis of finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphysis of the proximal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad phalanx Gene Set From HPO Gene-Disease Associations genes associated with the broad phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular epiphysis of the middle phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the middle phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short middle phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the short middle phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged epiphysis of the middle phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the middle phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal phalanx morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal phalanx morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Broad Hallux Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Broad Hallux Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Triangular Shaped Middle Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triangular Shaped Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Distal Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fifth Finger Distal Phalanx Clinodactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fifth Finger Distal Phalanx Clinodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Broad Middle Phalanx Of Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Broad Middle Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Triangular Shaped Distal Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triangular Shaped Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bifid Distal Phalanx Of Toe Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bifid Distal Phalanx Of Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Middle Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Long Phalanx Of Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Long Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypersegmentation Of Proximal Phalanx Of Second Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypersegmentation Of Proximal Phalanx Of Second Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypersegmentation Of Proximal Phalanx Of Third Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypersegmentation Of Proximal Phalanx Of Third Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Triangular Epiphysis Of The Middle Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triangular Epiphysis Of The Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Triangular Epiphysis Of The Proximal Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triangular Epiphysis Of The Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Triangular Shaped Proximal Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triangular Shaped Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Broad Distal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Broad Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Long Distal Phalanx Of Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Long Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Long Proximal Phalanx Of Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Long Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Slender Proximal Phalanx Of Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Slender Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bullet-Shaped Distal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bullet-Shaped Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Distal Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Phalanx Of Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Distal Phalanx Of Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Phalanx Of The Toes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Phalanx Of The Toes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Curved Toe Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Curved Toe Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Middle Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Proximal Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Middle Phalanx Of 5Th Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Middle Phalanx Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Patchy Sclerosis Of Finger Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Patchy Sclerosis Of Finger Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Middle Phalanx Of The 5Th Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Middle Phalanx Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Slender Distal Phalanx Of Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Proximal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Proximal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Curved 4Th Toe Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Curved 4Th Toe Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
abnormal phalanx morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal phalanx morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Symphalangism affecting the proximal phalanx of the 4th finger Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Symphalangism affecting the proximal phalanx of the 4th finger phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Harmonizome 3.0

DUP5P13 Gene

CXDUPQ26.3 Gene

OPHLC Gene

DUP16P11.2 Gene

DUP17Q23.1Q23.2 Gene

DUP2Q31.1 Gene

DUP16P13.3 Gene

DUPXQ28 Gene

DUP7Q11.23 Gene

DUPXQ27.3Q28 Gene

DUP17P13.3 Gene

DUP17Q12 Gene

DUPXP11.23P11.22 Gene

DUP1Q21 Gene

DUP17Q21.31 Gene

DUP8Q22.1 Gene

DUP22Q13 Gene

complete duplication of thumb phalanx Gene Set

Complete Duplication Of Thumb Phalanx Gene Set

complete duplication of proximal phalanx of the thumb Gene Set

complete duplication of distal phalanx of the thumb Gene Set

Complete Duplication Of Distal Phalanx Of The Thumb Gene Set

Complete Duplication Of Proximal Phalanx Of The Thumb Gene Set

duplication of the proximal phalanx of the thumb Gene Set

partial duplication of thumb phalanx Gene Set

duplication of the distal phalanx of the thumb Gene Set

duplication of thumb phalanx Gene Set

Duplication Of Thumb Phalanx Gene Set

Partial Duplication Of Thumb Phalanx Gene Set

complete duplication of phalanx of hand Gene Set

Complete Duplication Of The Middle Phalanx Of The 3Rd Finger Gene Set

Complete Duplication Of Hallux Phalanx Gene Set

abnormality of thumb phalanx Gene Set

broad distal phalanx of the thumb Gene Set

radial deviation of thumb terminal phalanx Gene Set

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

bifid distal phalanx of the thumb Gene Set

short phalanx of the thumb Gene Set

absent proximal phalanx of thumb Gene Set

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

short proximal phalanx of thumb Gene Set

abnormality of the distal phalanx of the thumb Gene Set

short distal phalanx of the thumb Gene Set

abnormality of the proximal phalanx of the thumb Gene Set

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

Radial Deviation Of Thumb Terminal Phalanx Gene Set

Bifid Distal Phalanx Of The Thumb Gene Set

Abnormality Of The Distal Phalanx Of The Thumb Gene Set

Absent Proximal Phalanx Of Thumb Gene Set

Broad Distal Phalanx Of The Thumb Gene Set

Abnormality Of The Proximal Phalanx Of The Thumb Gene Set

Triangular shaped proximal phalanx of the thumb Gene Set

complete duplication of the distal phalanges of the hand Gene Set

complete duplication of the middle phalanges of the hand Gene Set

Complete Duplication Of The Distal Phalanges Of The Hand Gene Set

duplication of phalanx of toe Gene Set

duplication of distal phalanx of toe Gene Set

duplication of the distal phalanx of hand Gene Set

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

partial duplication of the distal phalanx of the 3rd finger Gene Set

partial duplication of the distal phalanx of the 2nd finger Gene Set

duplication of middle phalanx of toe Gene Set

duplication of phalanx of 3rd finger Gene Set

duplication of phalanx of hand Gene Set

duplication of phalanx of 2nd finger Gene Set

duplication of the distal phalanx of the hallux Gene Set

duplication of the middle phalanx of hand Gene Set

duplication of the proximal phalanx of the hallux Gene Set

partial duplication of the distal phalanx of the hallux Gene Set

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

partial duplication of the phalanx of hand Gene Set

duplication of phalanx of hallux Gene Set

Partial Duplication Of The Distal Phalanx Of The 2Nd Finger Gene Set

Partial Duplication Of The Distal Phalanx Of The 3Rd Finger Gene Set

Duplication Of The Proximal Phalanx Of The Hallux Gene Set

Partial Duplication Of The Distal Phalanx Of The Hallux Gene Set

Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger Gene Set

Duplication Of Phalanx Of Hallux Gene Set

Duplication Of The Distal Phalanx Of Hand Gene Set