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Details
Link-It Detail - Human Phenotype - Abnormality of the 2nd finger
Debug Stats
  • ### Total Build Time: 17 ms 21.413 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 204 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 232 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=2 ms Completed: 2 ms rowSize= 442 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.117 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.928 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 13.343 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.023 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the 2nd finger HP:0004100
Definition (1)
An anomaly of the `second finger` (FMA:24946), also known as the index finger.
Parents (1)
img Abnormality of finger HP:0001167
Children (6)
img Abnormality of the epiphyses of the 2nd finger HP:0006263
img Aplasia/Hypoplasia of the 2nd finger HP:0006264
img Abnormality of the phalanges of the 2nd finger HP:0009541
img Flexion contracture of the 2nd finger HP:0009537
img Polydactyly affecting the 2nd finger HP:0009946
img Deviation of the 2nd finger HP:0009468
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of finger HP:0001167
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of finger HP:0001167
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanMSSD619407syndactyly, mesoaxial synostotic, with phalangeal reduction
img HP RolledUp, OMIM ID: 609432
HumanACRPV414058Acropectorovertebral dysplasia (F syndrome)
img HP RolledUp, OMIM ID: 102510
HumanBDA1B246260Brachydactyly, type A1, locus B
img HP RolledUp, OMIM ID: 112500
HumanIRX510265iroquois homeobox 5
img HP RolledUp, OMIM ID: 611174
HumanGDF58200growth differentiation factor 5
img HP RolledUp, OMIM ID: 112600
img HP RolledUp, OMIM ID: 113100
HumanTWIST17291twist basic helix-loop-helix transcription factor 1
img HP RolledUp, OMIM ID: 101400
HumanMYCN4613v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
img HP RolledUp, OMIM ID: 164280
HumanIHH3549indian hedgehog
img HP RolledUp, OMIM ID: 112500
HumanHOXA133209homeobox A13
img HP RolledUp, OMIM ID: 140000
HumanFLNA2316filamin A, alpha
img HP RolledUp, OMIM ID: 304120
HumanFGFR22263fibroblast growth factor receptor 2
img HP RolledUp, OMIM ID: 101400
HumanCOL2A11280collagen, type II, alpha 1
img HP RolledUp, OMIM ID: 271700
HumanRUNX2860runt-related transcription factor 2
img HP RolledUp, OMIM ID: 156510
HumanBMPR1B658bone morphogenetic protein receptor, type IB
img HP RolledUp, OMIM ID: 112600
HumanBMP2650bone morphogenetic protein 2
img HP RolledUp, OMIM ID: 112600
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004100Abnormality of the 2nd finger0self