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Details
Link-It Detail - Human Phenotype - Abnormality of the hallux
Debug Stats
  • ### Total Build Time: 40 ms 31.636 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 200 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 229 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=3 ms Completed: 3 ms rowSize= 439 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.718 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=11 ms Completed: 11 ms rowSize= 3.916 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 22.990 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the hallux HP:0001844
Definition (1)
This term applies for all abnormalities of the big toe, also called hallux.
Parents (1)
img Abnormality of toe HP:0001780
Children (8)
img Long hallux HP:0001847
img Abnormality of the epiphyses of the hallux HP:0010056
img Broad hallux HP:0010055
img Preaxial polydactyly of foot HP:0001841
img Aplasia/Hypoplasia of the hallux HP:0008362
img Abnormality of the phalanges of the hallux HP:0010057
img Flexion contracture of the hallux HP:0010212
img Deviation/Displacement of the hallux HP:0010051
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of toe HP:0001780
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of toe HP:0001780
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of toe HP:0001780
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of toe HP:0001780
Genes (79)

Species:
human : 79
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
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
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP RolledUp, OMIM ID: 610543
HumanSHFL1791121Split-hand/foot malformation with long bone deficiency 1
img HP RolledUp, OMIM ID: 119100
HumanMSSD619407syndactyly, mesoaxial synostotic, with phalangeal reduction
img HP RolledUp, OMIM ID: 609432
HumanKIF7374654kinesin family member 7
img HP RolledUp, OMIM ID: 200990
HumanSUMF1285362sulfatase modifying factor 1
img HP RolledUp, OMIM ID: 272200
HumanBDA1B246260Brachydactyly, type A1, locus B
img HP RolledUp, OMIM ID: 607004
img HP RolledUp, OMIM ID: 112500
HumanHYLS1219844hydrolethalus syndrome 1
img HP RolledUp, OMIM ID: 236680
HumanMIPOL1145282mirror-image polydactyly 1
img HP RolledUp, OMIM ID: 135750
HumanB3GALT6126792UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
img HP RolledUp, OMIM ID: 271640
HumanCANT1124583calcium activated nucleotidase 1
img HP RolledUp, OMIM ID: 251450
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanSCARF291179scavenger receptor class F, member 2
img HP RolledUp, OMIM ID: 600920
HumanDYNC2H179659dynein, cytoplasmic 2, heavy chain 1
img HP RolledUp, OMIM ID: 263520
HumanLMBR164327limb development membrane protein 1
img HP RolledUp, OMIM ID: 174500
HumanSALL457167sal-like 4 (Drosophila)
img HP RolledUp, OMIM ID: 607323
HumanFAM20C56975family with sequence similarity 20, member C
img HP RolledUp, OMIM ID: 259775
HumanSLC29A355315solute carrier family 29 (equilibrative nucleoside transporter), member 3
img HP RolledUp, OMIM ID: 602782
HumanRAB2351715RAB23, member RAS oncogene family
img HP RolledUp, OMIM ID: 201000
HumanMLXIPL51085MLX interacting protein-like
img HP RolledUp, OMIM ID: 194050
HumanSF3B410262splicing factor 3b, subunit 4, 49kDa
img HP RolledUp, OMIM ID: 154400
HumanABCC910060ATP-binding cassette, sub-family C (CFTR/MRP), member 9
img HP RolledUp, OMIM ID: 239850
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001844Abnormality of the hallux0self