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Details
Link-It Detail - Human Phenotype - Abnormal hair pattern
Debug Stats
  • ### Total Build Time: 69 ms 31.248 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 196 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 204 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=16 ms Completed: 16 ms rowSize= 770 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 3.575 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 3.935 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=39 ms Completed: 39 ms rowSize= 21.436 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.016 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal hair pattern HP:0010720
Definition (1)
An abnormality of the distribution of hair growth.
Parents (2)
img Abnormality of the hair HP:0001595
img Abnormality of the skin HP:0000951
Children (11)
img Facial hypertrichosis HP:0002219
img Early balding HP:0002234
img Hypotrichosis HP:0001006
img Synophrys HP:0000664
img Frontal balding HP:0002292
img Hirsutism HP:0001007
img Abnormal hair whorl HP:0010721
img Congenital abnormal hair pattern HP:0011361
img Acquired abnormal hair pattern HP:0011360
img Hypertrichosis HP:0000998
img Abnormality of the hairline HP:0009553
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:00001185img Abnormality of the skin HP:0000951
Genes (296)

Species:
human : 296
Page Size
Current 25
  Page 1 of 12
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanECTD7101101771Ectodermal dysplasia 7, hair/nail type
img HP RolledUp, OMIM ID: 614929
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
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
HumanKONDS100653373Kondoh syndrome
HumanDUP17Q21.31100529226
img HP RolledUp, OMIM ID: 613533
HumanMMRFCGU100529147Microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations
img HP RolledUp, OMIM ID: 613680
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanEDSS2100505394Ectodermal dysplasia-syndactyly syndrome 2
img HP RolledUp, OMIM ID: 613576
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanHTGH100302716Hypertrichosis terminalis, generalized, with or without gingival hyperplasia
img HP RolledUp, OMIM ID: 135400
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 RolledUp, OMIM ID: 607872
HumanDEL18Q100216483Chromosome 18q deletion syndrome
HumanMICRODEL15Q13.3100188869
img HP RolledUp, OMIM ID: 612001
HumanDUP3Q29100188862chromosome 3q29 microduplication syndrome
HumanMRT5100188831mental retardation, non-syndromic, autosomal recessive, 5
img HP RolledUp, OMIM ID: 611091
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP RolledUp, OMIM ID: 610543
HumanITC1100188785hypertrichosis universalis congenita, Ambras type
HumanAA1100034700Alopecia areata 1
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010720Abnormal hair pattern0self