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Details
Link-It Detail - Human Phenotype - Abnormal hair quantity
Debug Stats
  • ### Total Build Time: 41 ms 27.623 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 197 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 181 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=4 ms Completed: 4 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.041 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=28 ms Completed: 28 ms rowSize= 21.608 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.017 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal hair quantity HP:0011362
Definition (1)
An abnormal amount of hair.
Parents (1)
img Abnormality of the hair HP:0001595
Children (3)
img Hypertrichosis HP:0000998
img Hypotrichosis HP:0001006
img Hirsutism HP:0001007
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 (219)

Species:
human : 219
Page Size
Current 25
  Page 1 of 9
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanECTD7101101771Ectodermal dysplasia 7, hair/nail type
img HP RolledUp, OMIM ID: 614929
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
HumanDUP17Q21.31100529226
img HP RolledUp, OMIM ID: 613533
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanEDSS2100505394Ectodermal dysplasia-syndactyly syndrome 2
img HP RolledUp, OMIM ID: 613576
HumanHTGH100302716Hypertrichosis terminalis, generalized, with or without gingival hyperplasia
img HP RolledUp, OMIM ID: 135400
HumanDEL9P100240748Chromosome 9p deletion syndrome
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanMICRODEL15Q13.3100188869
HumanMRT5100188831mental retardation, non-syndromic, autosomal recessive, 5
img HP RolledUp, OMIM ID: 611091
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
HumanITC1100188785hypertrichosis universalis congenita, Ambras type
HumanCHMRQ780925Cerebellar hypoplasia, mental retardation, and quadrupedal locomotion
img HP RolledUp, OMIM ID: 610185
HumanNDUFS7374291NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
img HP RolledUp, OMIM ID: 256000
HumanZLS353173Zimmerman-Laband Syndrome
img HP RolledUp, OMIM ID: 135500
HumanPTRF284119polymerase I and transcript release factor
img HP RolledUp, OMIM ID: 613327
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanARX170302aristaless related homeobox
img HP RolledUp, OMIM ID: 300004
HumanBBS12166379Bardet-Biedl syndrome 12
img HP RolledUp, OMIM ID: 209900
HumanAPCDD1147495adenomatosis polyposis coli down-regulated 1
img HP RolledUp, OMIM ID: 605389
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011362Abnormal hair quantity0self