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Details
Link-It Detail - Disease - Facies
Debug Stats
  • ### Total Build Time: 114 ms 16.490 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 310 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 376 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= 187 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 554 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 1.528 KB
  • CONCEPT_RELATIONSHIPS gt=85 ms Completed: 85 ms rowSize= 12.349 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.141 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Facies C0282631
Definition (1)
The appearance of the face that is often characteristic of a disease or pathological condition, as the elfin facies of WILLIAMS SYNDROME or the mongoloid facies of DOWN SYNDROME. (Random House Unabridged Dictionary, 2d ed)
Semantic Types (1)
Organism Attribute (T032)
Parents (1)
img Disease Attributes C0752357
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathologic Processes C00306604img Disease Attributes C0752357
Relationships (99)

Relation Types:
phys_​to_​anat : 5
phys_​to_​diso : 93
phys_​to_​phys : 1


Relationships:
none : 32
mapped_​to : 67
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
PHYS_to_DISO34img Abnormalities, Multiple C0000772
PHYS_to_DISO24img Abnormalities, Multiple C0000772
PHYS_to_DISO22img Intellectual Disability C0025362
PHYS_to_DISO15img Intellectual Disability C0025362
PHYS_to_DISO13img Abnormalities, Craniofacial C0376634
PHYS_to_DISO12img Developmental Disabilities C0008073
PHYS_to_DISO10img Developmental Disabilities C0008073
PHYS_to_DISO8img Chromosome Deletion C0008628
PHYS_to_DISO7img CL - Cleft lip C0008924
PHYS_to_DISO7img Cleft Palate C0008925
PHYS_to_DISO7img Congenital Heart Defects C0018798
PHYS_to_DISO7img Disorder, Growth C0018273
PHYS_to_DISO7img Fetal Alcohol Syndrome C0015923
PHYS_to_DISO7img MICROCEPHALY C0025958
PHYS_to_ANAT6img Face C0015450
PHYS_to_DISO6img Congenital Heart Defects C0018798
PHYS_to_DISO6img Disorder, Growth C0018273
PHYS_to_ANAT5img 22 chromosome C0008665
PHYS_to_ANAT5img Brain C0006104
PHYS_to_DISO5img 4-40 CONGENITAL ANOMALIES OF THE SKIN C0037268
PHYS_to_DISO5img Muscle Hypotonia C0026827
PHYS_to_ANAT4img Facial Muscles C0015460
PHYS_to_ANAT4img Femur C0015811
PHYS_to_DISO4img ABNORM MAXILLOFACIAL C0524948
PHYS_to_DISO4img Abnormalities, Craniofacial C0376634
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0282631Facies0self