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Details
Link-It Detail - Human Phenotype - Abnormality of the eyelid
Debug Stats
  • ### Total Build Time: 57 ms 35.218 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 200 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 198 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=4 ms Completed: 4 ms rowSize= 793 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 6.721 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 3.046 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=42 ms Completed: 42 ms rowSize= 23.124 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the eyelid HP:0000492
Definition (1)
An abnormality of the `eyelids` (FMA:75178).
Parents (2)
img Abnormality of the periorbital region HP:0000606
img Abnormality of the ocular region HP:0000284
Children (21)
img Epicanthus inversus HP:0000537
img Puffy eyelids HP:0000626
img Palpebral edema HP:0100540
img Blepharitis HP:0000498
img Abnormality of the palpebral fissures HP:0008050
img Epicanthus HP:0000286
img Abnormality of the eyelashes HP:0000499
img Eyelid apraxia HP:0000658
img Blepharospasm HP:0000643
img Telecanthus HP:0000506
img Hypoplasia of the lower eyelids HP:0007697
img Epiblepharon HP:0011225
img Aplasia of the eyelids HP:0009925
img Aplasia/Hypoplasia affecting the eyelid HP:0011226
img Ankyloblepharon HP:0009755
img Ectropion HP:0000656
img Cleft eyelid HP:0000625
img Entropion HP:0000621
img Dermatochalasis HP:0010750
img Nodular changes affecting the eyelids HP:0010732
img Blepharochalasis HP:0010749
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the periorbital region HP:0000606
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the periorbital region HP:0000606
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the ocular region HP:0000284
Genes (549)

Species:
human : 549
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
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
HumanC16DELQ22100874527Chromosome 16q22 deletion syndrome
img HP RolledUp, OMIM ID: 614541
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanTET18P100750329Tetrasomy 18p
img HP RolledUp, OMIM ID: 614290
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP RolledUp, OMIM ID: 613884
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanDEL1Q41Q42100529242Chromosome 1q41-q42 deletion syndrome
img HP RolledUp, OMIM ID: 612530
HumanTRIP4Q32.1Q32.2100529228
img HP RolledUp, OMIM ID: 613603
HumanDUP17Q21.31100529226
img HP RolledUp, OMIM ID: 613533
HumanDEL6Q11Q14100529221Chromosome 6q11-q14 deletion syndrome
img HP RolledUp, OMIM ID: 613544
HumanMMRFCGU100529147Microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations
img HP RolledUp, OMIM ID: 613680
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanDUP16P13.3100505393
img HP RolledUp, OMIM ID: 613458
HumanDEL14Q11Q22100505392Chromosome 14q11-q22 deletion syndrome
img HP RolledUp, OMIM ID: 613457
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000492Abnormality of the eyelid0self