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Details
Link-It Detail - Disease - Plagiocephaly
Debug Stats
  • ### Total Build Time: 12 ms 9.266 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 324 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 442 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= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=8 ms Completed: 8 ms rowSize= 3.430 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 3.870 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.147 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Disease (1)
Plagiocephaly C0265529
Definition (1)
The condition characterized by uneven or irregular shape of the head often in parallelogram shape with a flat spot on the back or one side of the head. It can either result from the premature CRANIAL SUTURE closure (CRANIOSYNOSTOSIS) or from external forces (NONSYNOSTOTIC PLAGIOCEPHALY).
Relationships (5)

Relation Types:
diso_​to_​anat : 1
diso_​to_​diso : 4


Relationships:
none : 1
associated_​with : 1
isa : 1
location_​of : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO3img Craniosynostoses C0010278
DISO_to_ANATlocation_ofimg Head C0018670
DISO_to_DISOassociated_withimg Congenital disproportion C0332902
DISO_to_DISOisaimg Congenital plagiocephaly with pelvic obliquity C1827229
DISO_to_DISOpermuted_term_ofimg Plagiocephaly C0265529
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanTWIST17291twist basic helix-loop-helix transcription factor 1
img OMIM, Score=1000, UMLKSK CUI: C0265529
HumanFGFR22263fibroblast growth factor receptor 2
img OMIM, Score=1000, UMLKSK CUI: C0265529
HumanFGFR32261fibroblast growth factor receptor 3
img OMIM, Score=1000, UMLKSK CUI: C0265529
HumanBMP4652bone morphogenetic protein 4
img OMIM, Score=1000, UMLKSK CUI: C0265529
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0265529Plagiocephaly0self