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Details
Link-It Detail - Human Phenotype - Abnormality of the eyebrow
Debug Stats
  • ### Total Build Time: 49 ms 37.302 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 201 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 198 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=6 ms Completed: 6 ms rowSize= 1.094 KB
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 5.826 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 5.821 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 23.006 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the eyebrow HP:0000534
Definition (1)
An abnormality of the `eyebrow` (FMA:54237).
Parents (3)
img Abnormality of the hair HP:0001595
img Abnormality of the periorbital region HP:0000606
img Abnormality of the ocular region HP:0000284
Children (18)
img Laterally curved eyebrow HP:0007733
img Broad lateral eyebrow HP:0007933
img Laterally extended eyebrow HP:0011230
img Lateral thinning of eyebrows HP:0009923
img Absent eyebrow HP:0002223
img Extension of eyebrows towards upper eyelid HP:0010731
img Medial flaring of the eyebrow HP:0010747
img White eyebrow HP:0002226
img Thick eyebrow HP:0000574
img Highly arched eyebrow HP:0002553
img Horizontal eyebrow HP:0011228
img Aplasia/Hypoplasia of the eyebrow HP:0100840
img Broad eyebrow HP:0011229
img Thin eyebrows HP:0002554
img Sparse eyebrow HP:0000535
img Long eyebrows HP:0004523
img Bowed and upward slanting eyebrows HP:0008505
img Double eyebrow HP:0010730
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
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the periorbital region HP:0000606
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the periorbital region HP:0000606
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the ocular region HP:0000284
Genes (240)

Species:
human : 240
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanECTD7101101771Ectodermal dysplasia 7, hair/nail type
img HP RolledUp, OMIM ID: 614929
HumanECTD8101101768Ectodermal dysplasia 8, hair/tooth/nail type
img HP RolledUp, OMIM ID: 602401
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
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanMRXSCS100820761Mental retardation, X-linked, syndromic, Chudley-Schwartz type
img HP RolledUp, OMIM ID: 300861
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanKONDS100653373Kondoh syndrome
img HP RolledUp, OMIM ID: 606242
HumanDUP17Q21.31100529226
img HP RolledUp, OMIM ID: 613533
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP TAS, OMIM ID: 600383
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP RolledUp, OMIM ID: 613457
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP TAS, OMIM ID: 613406
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanHTGH100302716Hypertrichosis terminalis, generalized, with or without gingival hyperplasia
img HP RolledUp, OMIM ID: 135400
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 TAS, OMIM ID: 607872
HumanMICRODEL15Q13.3100188869
img HP RolledUp, OMIM ID: 612001
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000534Abnormality of the eyebrow0self