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Details
Link-It Detail - Human Phenotype - Abnormality of the hairline
Debug Stats
  • ### Total Build Time: 31 ms 35.486 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 390 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=2 ms Completed: 2 ms rowSize= 1.084 KB
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.104 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 8.600 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 22.955 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the hairline HP:0009553
Definition (1)
The hairline refers to the outline of `hair of the head` (FMA:54241). An abnormality of the hairline can refer to an unusually low or high border between areas of the scalp with and without hair or to abnormal projections of scalp hair.
Parents (3)
img Abnormal hair pattern HP:0010720
img Congenital abnormal hair pattern HP:0011361
img Abnormality of the scalp hair HP:0100037
Children (3)
img Abnormality of the frontal hairline HP:0000599
img Low posterior hairline HP:0002162
img Projection of scalp hair onto lateral cheek HP:0009554
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormal hair pattern HP:0010720
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormal hair pattern HP:0010720
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormal hair pattern HP:0010720
img All HP:0000001img Phenotypic abnormality HP:00001187img Congenital abnormal hair pattern HP:0011361
img All HP:0000001img Phenotypic abnormality HP:00001189img Congenital abnormal hair pattern HP:0011361
img All HP:0000001img Phenotypic abnormality HP:00001188img Congenital abnormal hair pattern HP:0011361
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the scalp hair HP:0100037
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the scalp hair HP:0100037
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the scalp hair HP:0100037
Genes (83)

Species:
human : 83
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanKONDS100653373Kondoh syndrome
img HP RolledUp, OMIM ID: 606242
HumanMMRFCGU100529147Microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations
img HP RolledUp, OMIM ID: 613680
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL18P100240747Chromosome 18p deletion syndrome
img HP RolledUp, OMIM ID: 146390
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP PCS, OMIM ID: 607872
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
img HP RolledUp, OMIM ID: 611936
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP PCS, OMIM ID: 610543
HumanTQDS780911Chromosome 10q deletion syndrome
img HP RolledUp, OMIM ID: 609625
HumanGDF6392255growth differentiation factor 6
img HP RolledUp, OMIM ID: 214300
img HP RolledUp, OMIM ID: 118100
HumanZLS353173Zimmerman-Laband Syndrome
img HP RolledUp, OMIM ID: 135500
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img HP RolledUp, OMIM ID: 219000
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanARX170302aristaless related homeobox
img HP RolledUp, OMIM ID: 300004
HumanSPRED1161742sprouty-related, EVH1 domain containing 1
img HP RolledUp, OMIM ID: 611431
HumanZDHHC15158866zinc finger, DHHC-type containing 15
img HP RolledUp, OMIM ID: 300577
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanFRAS180144Fraser syndrome 1
img HP RolledUp, OMIM ID: 219000
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP RolledUp, OMIM ID: 117550
HumanDOCK657572dedicator of cytokinesis 6
img HP RolledUp, OMIM ID: 614219
HumanZC4H255906zinc finger, C4H2 domain containing
img HP RolledUp, OMIM ID: 314580
HumanHDAC855869histone deacetylase 8
img HP RolledUp, OMIM ID: 300882
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0009553Abnormality of the hairline0self