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Details
Link-It Detail - Human Phenotype - Abnormality of hair texture
Debug Stats
  • ### Total Build Time: 40 ms 31.541 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 210 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=5 ms Completed: 5 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 3.193 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.010 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=29 ms Completed: 29 ms rowSize= 23.336 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of hair texture HP:0010719
Definition (1)
An abnormality of the texture of the `hair` (FMA:53667).
Parents (1)
img Abnormality of the hair HP:0001595
Children (10)
img Curly hair HP:0002212
img Dry hair HP:0011359
img Thin hair HP:0002237
img Brittle hair HP:0002299
img Coarse hair HP:0002208
img Fine hair HP:0002213
img Pili torti HP:0003777
img Pili canaliculi HP:0002235
img Woolly hair HP:0002224
img Trichorrhexis nodosa HP:0009886
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the hair HP:0001595
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the hair HP:0001595
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the hair HP:0001595
Genes (134)

Species:
human : 134
Page Size
Current 25
  Page 1 of 6
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Current 1
SpeciesGeneGeneIdGene NameEvidence
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
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanHRM2100379199hair, curly
img HP RolledUp, OMIM ID: 139450
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDEL2Q32Q33100190983Chromosome 2q32-q33 deletion syndrome
img HP RolledUp, OMIM ID: 612313
HumanAGSPX100188767Angio serpiginosum
img HP RolledUp, OMIM ID: 300652
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanDEL17Q21.31791085
img HP TAS, OMIM ID: 610443
HumanCDAGS574043Craniosynostosis, anal anomalies, and porokeratosis syndrome
img HP RolledUp, OMIM ID: 603116
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
img HP IEA, OMIM ID: 601675
HumanSUMF1285362sulfatase modifying factor 1
img HP RolledUp, OMIM ID: 272200
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP TAS, OMIM ID: 610443
HumanLIPH200879lipase, member H
img HP RolledUp, OMIM ID: 604379
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanDSG4147409desmoglein 4
img HP RolledUp, OMIM ID: 607903
HumanHGSNAT138050heparan-alpha-glucosaminide N-acetyltransferase
img HP RolledUp, OMIM ID: 252930
HumanMPLKIP136647M-phase specific PLK1 interacting protein
img HP IEA, OMIM ID: 234050
HumanEDARADD128178EDAR-associated death domain
img HP RolledUp, OMIM ID: 224900
img HP RolledUp, OMIM ID: 129490
HumanB3GALT6126792UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
img HP RolledUp, OMIM ID: 271640
HumanKRT74121391keratin 74
img HP RolledUp, OMIM ID: 194300
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010719Abnormality of hair texture0self