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Details
Link-It Detail - Human Phenotype - Abnormality of the face
Debug Stats
  • ### Total Build Time: 102 ms 35 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 198 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=0 Completed: 0 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 8.426 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.159 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=94 ms Completed: 94 ms rowSize= 23.626 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.018 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the face HP:0000271
Parents (1)
img Abnormality of the head HP:0000234
Children (26)
img Abnormality of the orbital region HP:0000315
img Facial cleft HP:0002006
img Abnormality of the mouth HP:0000153
img Abnormal facial shape HP:0001999
img Abnormality of facial musculature HP:0000301
img Facial hemangioma HP:0000329
img Abnormality of facial adipose tissue HP:0000291
img Abnormality of the forehead HP:0000290
img Abnormal facial expression HP:0005346
img Atrophodermia vermiculata HP:0100837
img Craniofacial dysostosis HP:0004439
img Abnormality of the periorbital region HP:0000606
img Hemifacial hypertrophy HP:0005323
img Mask-like facies HP:0000298
img Facial asymmetry HP:0000324
img Craniofacial hyperostosis HP:0004493
img Facial edema HP:0000282
img Abnormality of the chin HP:0000306
img Progeroid facial appearance HP:0005328
img Bitemporal narrowing HP:0000314
img Adenoma sebaceum HP:0009720
img Facial palsy HP:0010628
img Abnormality of the ocular region HP:0000284
img Abnormality of the nose HP:0000366
img Abnormality of the midface HP:0000309
img Abnormality of facial soft tissue HP:0011799
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the head HP:0000234
Genes (1435)

Species:
human : 1435
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
HumanPDA1100996949Patent ductus arteriosus, susceptibility to
img HP RolledUp, OMIM ID: 607411
HumanDUP16P11.2100909384
img HP RolledUp, OMIM ID: 614671
HumanOTDD100885788Otodental dysplasia chromsome deletion syndrome
img HP RolledUp, OMIM ID: 166750
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanDYT21100885773dystonia 21, torsion (autosomal dominant)
img HP RolledUp, OMIM ID: 614588
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
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
img HP RolledUp, OMIM ID: 614541
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanCPBHM100820762Chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia
img HP RolledUp, OMIM ID: 300863
HumanMRXSCS100820761Mental retardation, X-linked, syndromic, Chudley-Schwartz type
img HP RolledUp, OMIM ID: 300861
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanSCA34100750330spinocerebellar ataxia 34
img HP RolledUp, OMIM ID: 133190
HumanTET18P100750329Tetrasomy 18p
img HP RolledUp, OMIM ID: 614290
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanHPPD100682260Hypertelorism, preauricular sinus, punctal pits, and deafness
img HP RolledUp, OMIM ID: 614187
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP RolledUp, OMIM ID: 613884
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000271Abnormality of the face0self