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Details
Link-It Detail - Human Phenotype - Abnormality of phalanx of finger
Debug Stats
  • ### Total Build Time: 83 ms 37.652 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 207 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 214 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=1 ms Completed: 1 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= 442 bytes
  • CONCEPT_CHILDREN gt=19 ms Completed: 19 ms rowSize= 8.817 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.928 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=50 ms Completed: 50 ms rowSize= 22.894 KB
  • CONCEPT_XREFS gt=9 ms Completed: 9 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of phalanx of finger HP:0005918
Definition (1)
Abnormalities affecting the `phalanx of finger` (FMA:23914).
Parents (1)
img Abnormality of finger HP:0001167
Children (26)
img Irregular phalanges HP:0006205
img Broad phalanges of the hand HP:0009768
img Sclerosis of the phalanges of the hand HP:0100899
img Duplication of phalanx of hand HP:0009997
img Tapered phalanx of finger HP:0006192
img Abnormality of the epiphyses of the phalanges of the hand HP:0005920
img Long phalanx of finger HP:0006155
img Abnormality of phalangeal joints of the hand HP:0006261
img Aplasia/Hypoplasia of the phalanges of the hand HP:0009767
img Abnormality of the proximal phalanges of the hand HP:0009834
img Abnormality of the phalanges of the 4th finger HP:0009172
img Abnormality of the phalanges of the 3rd finger HP:0009316
img Abnormality of the phalanges of the 5th finger HP:0004213
img Hypersegmentation of proximal phalanx of second finger HP:0006206
img Abnormality of the phalanges of the 2nd finger HP:0009541
img Symphalangism affecting the phalanges of the hand HP:0009773
img Bullet-shaped phalanges of the hand HP:0009769
img Phalangeal dislocations HP:0006243
img Osteolytic defects of the phalanges of the hand HP:0009771
img Curved phalanges of the hand HP:0009770
img Patchy sclerosis of the phalanges of the hand HP:0009772
img Abnormality of the distal phalanx of finger HP:0009832
img Abnormality of the middle phalanges of the hand HP:0009833
img Partial absence of finger HP:0011299
img Abnormality of the phalanges of the thumb HP:0009602
img Triangular shaped phalanges of the hand HP:0009774
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of finger HP:0001167
Genes (362)

Species:
human : 362
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SpeciesGeneGeneIdGene NameEvidence
HumanPAPA5101241897Polydactyly, postaxial, type A5
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
img HP RolledUp, OMIM ID: 614526
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanKONDS100653373Kondoh syndrome
img HP RolledUp, OMIM ID: 606242
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
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
HumanCAMPD1100381210Camptodactyly 1
img HP RolledUp, OMIM ID: 114200
HumanDEL15Q26QTER100271921Chromosome 15q26-qter deletion syndrome
img HP RolledUp, OMIM ID: 612626
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDEL1Q21100217370Chromosome 1q21.1 deletion syndrome
img HP RolledUp, OMIM ID: 612474
HumanJAWAD100192306Microcephaly with digital anomalies
img HP RolledUp, OMIM ID: 251255
HumanDEL2Q32Q33100190983Chromosome 2q32-q33 deletion syndrome
img HP RolledUp, OMIM ID: 612313
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP RolledUp, OMIM ID: 610543
HumanAUTS14100187724autism, susceptibility to, 14
img HP RolledUp, OMIM ID: 611913
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP RolledUp, OMIM ID: 149000
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0005918Abnormality of phalanx of finger0self