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Details
Link-It Detail - Human Phenotype - Abnormality of facial adipose tissue
Debug Stats
  • ### Total Build Time: 22 ms 11.867 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 211 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=5 ms Completed: 5 ms rowSize= 1.087 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 786 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 3.025 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 5.606 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.030 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of facial adipose tissue HP:0000291
Parents (3)
img Abnormality of the face HP:0000271
img Abnormality of adipose tissue HP:0009124
img Abnormality of facial soft tissue HP:0011799
Children (2)
img Increased facial adipose tissue HP:0000287
img Loss of facial adipose tissue HP:0000292
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the face HP:0000271
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of adipose tissue HP:0009124
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of facial soft tissue HP:0011799
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanLMNB284823lamin B2
img HP RolledUp, OMIM ID: 608709
HumanZMPSTE2410269zinc metallopeptidase STE24
img HP RolledUp, OMIM ID: 608612
HumanPPARG5468peroxisome proliferator-activated receptor gamma
img HP RolledUp, OMIM ID: 151660
HumanLMNA4000lamin A/C
img HP RolledUp, OMIM ID: 248370
img HP RolledUp, OMIM ID: 151660
HumanERCC62074excision repair cross-complementing rodent repair deficiency, complementation group 6
img HP RolledUp, OMIM ID: 133540
HumanERCC81161excision repair cross-complementing rodent repair deficiency, complementation group 8
img HP RolledUp, OMIM ID: 216400
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000291Abnormality of facial adipose tissue0self