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Details
Link-It Detail - Human Phenotype - Abnormality of the hair
Debug Stats
  • ### Total Build Time: 74 ms 33.113 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 198 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 195 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=8 ms Completed: 8 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 779 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 4.626 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.021 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=53 ms Completed: 53 ms rowSize= 23.159 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.018 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the hair HP:0001595
Definition (1)
An abnormality of the `hair` (FMA:53667).
Parents (2)
img Abnormality of the integument HP:0001574
img Abnormality of skin adnexa HP:0011138
Children (14)
img Abnormality of the eyelashes HP:0000499
img Sparse or absent hair HP:0002115
img Abnormality of the eyebrow HP:0000534
img Trichodysplasia HP:0002552
img Abnormal hair pattern HP:0010720
img Abnormality of hair density HP:0011357
img Abnormality of hair growth rate HP:0011363
img Abnormal hair laboratory examination HP:0003328
img Abnormality of hair pigmentation HP:0009887
img Abnormality of hair texture HP:0010719
img Abnormality of the scalp hair HP:0100037
img Slow-growing hair HP:0002217
img Abnormality of secondary sexual hair HP:0009888
img Abnormal hair quantity HP:0011362
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the integument HP:0001574
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of skin adnexa HP:0011138
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of skin adnexa HP:0011138
Genes (612)

Species:
human : 612
Page Size
Current 25
  Page 1 of 25
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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
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
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
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
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanKONDS100653373Kondoh syndrome
img HP RolledUp, OMIM ID: 606242
HumanAPMR3100653369Alopecia-mental retardation syndrome 3
img HP RolledUp, OMIM ID: 613930
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
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanEDSS2100505394Ectodermal dysplasia-syndactyly syndrome 2
img HP RolledUp, OMIM ID: 613576
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP RolledUp, OMIM ID: 613457
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001595Abnormality of the hair0self