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Details
Link-It Detail - Human Phenotype - Abnormality of finger
Debug Stats
  • ### Total Build Time: 59 ms 37.146 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 196 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 190 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 772 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 7.793 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.938 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=45 ms Completed: 45 ms rowSize= 23.123 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.016 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of finger HP:0001167
Definition (1)
Abnormality of hands, feet, or both.
Parents (2)
img Abnormality of the hand HP:0001155
img Abnormality of the digits HP:0011297
Children (24)
img Abnormality of phalanx of finger HP:0005918
img Abnormality of the fingertips HP:0001211
img Long fingers HP:0100807
img Duplication of phalanx of hand HP:0009997
img Abnormality of the 4th finger HP:0004188
img Trident abnormality HP:0004060
img Curved fingers HP:0004095
img Short, broad fingers HP:0001497
img Abnormality of the 5th finger HP:0004207
img Abnormality of the fingernails HP:0001231
img Slender finger HP:0001238
img Abnormality of the 3rd finger HP:0004150
img Deviation of finger HP:0004097
img Swan neck-like deformities of the fingers HP:0006150
img Aplasia/Hypoplasia of fingers HP:0006265
img Abnormality of the thumb HP:0001172
img Abnormality of the 2nd finger HP:0004100
img Macrodactyly of finger HP:0100746
img Chilblain lesions HP:0009710
img Tapered finger HP:0001182
img Broad finger HP:0001500
img Abnormal finger flexion creases HP:0006143
img Hyperextensibility of the finger joints HP:0001187
img Macrodactyly HP:0004099
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the hand HP:0001155
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the hand HP:0001155
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the digits HP:0011297
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the digits HP:0011297
Genes (618)

Species:
human : 618
Page Size
Current 25
  Page 1 of 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanPAPA5101241897Polydactyly, postaxial, type A5
img HP RolledUp, OMIM ID: 263450
HumanECTD7101101771Ectodermal dysplasia 7, hair/nail type
img HP RolledUp, OMIM ID: 614929
HumanECTD5101101769Ectodermal dysplasia 5, hair/nail type
img HP RolledUp, OMIM ID: 614927
HumanECTD8101101768Ectodermal dysplasia 8, hair/tooth/nail type
img HP RolledUp, OMIM ID: 602401
HumanPDA1100996949Patent ductus arteriosus, susceptibility to
img HP RolledUp, OMIM ID: 607411
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanNDNC9100682325Nail disorder, nonsyndromic congenital, 9
img HP RolledUp, OMIM ID: 614149
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP RolledUp, OMIM ID: 613884
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanKONDS100653373Kondoh syndrome
img HP RolledUp, OMIM ID: 606242
HumanDUP17Q21.31100529226
img HP RolledUp, OMIM ID: 613533
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanDUP16P13.3100505393
img HP RolledUp, OMIM ID: 613458
HumanDEL6Q24Q25100505391Chromosome 6q25-q25 deletion syndrome
img HP RolledUp, OMIM ID: 612863
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
img HP RolledUp, OMIM ID: 300194
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001167Abnormality of finger0self