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Details
Link-It Detail - Disease - Gastroschisis
Debug Stats
  • ### Total Build Time: 45 ms 21.309 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 324 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 393 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= 247 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 1,000 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 4.166 KB
  • CONCEPT_RELATIONSHIPS gt=26 ms Completed: 26 ms rowSize= 12.691 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 1.351 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.147 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Gastroschisis C0265706
Definition (1)
A congenital defect with major fissure in the ABDOMINAL WALL lateral to, but not at, the UMBILICUS. This results in the extrusion of VISCERA. Unlike OMPHALOCELE, herniated structures in gastroschisis are not covered by a sac or PERITONEUM.
Semantic Types (2)
Congenital Abnormality (T019)
Disease or Syndrome (T047)
Parents (2)
img Hernia, Abdominal C0178282
img Musculoskeletal Abnormalities C0151491
Ancestral Roots
RootRoot Plus OneDepthParent
img Pathological Conditions, Signs and Symptoms C0039058img Pathological Conditions, Anatomical C07521355img Hernia, Abdominal C0178282
img Musculoskeletal Diseases C0026857img Musculoskeletal Abnormalities C01514913img Musculoskeletal Abnormalities C0151491
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007684img Musculoskeletal Abnormalities C0151491
Relationships (27)

Relation Types:
diso_​to_​anat : 8
diso_​to_​diso : 17
diso_​to_​phen : 2


Relationships:
none : 20
associated_​with : 2
expanded_​form_​of : 1
location_​of : 2
mapped_​to : 1
related_​to : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO62img Complication Aspects C1171258
DISO_to_DISO42img Congenital exomphalos C1306503
DISO_to_DISO36img Complication Aspects C1171258
DISO_to_DISO33img Congenital exomphalos C1306503
DISO_to_ANAT28img Abdominal Wall C0836916
DISO_to_DISO20img Abnormalities, Multiple C0000772
DISO_to_ANAT16img Intestines C0021853
DISO_to_DISO16img DISORDER FETAL C0015929
DISO_to_PHEN15img genetic aspects C0017399
DISO_to_ANAT14img Amniotic Fluid C0002638
DISO_to_ANAT13img Abdominal Wall C0836916
DISO_to_DISO13img Intestinal Atresia C0021828
DISO_to_ANAT10img Meconium C0025047
DISO_to_DISO10img Abnormalities, Multiple C0000772
DISO_to_DISO9img COMPL POSTOP C0032787
DISO_to_DISO9img Pregnancy Complications C0032962
DISO_to_PHEN9img genetic aspects C0017399
DISO_to_ANAT8img Amniotic Fluid C0002638
DISO_to_DISO7img Intestinal Atresia C0021828
DISO_to_DISO7img Intestinal Diseases C0021831
DISO_to_ANATlocation_ofimg Abdominal Wall C0836916
DISO_to_ANATlocation_ofimg Intestines C0021853
DISO_to_DISOrelated_toimg ABDOMINAL WALL DEFECT C0238577
DISO_to_DISOexpanded_form_ofimg Congenital Fissure of the Abdominal Cavity C0265706
DISO_to_DISOassociated_withimg Congenital failure of fusion C0332915
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanWNT37473wingless-type MMTV integration site family, member 3
img OMIM, Score=1000, UMLKSK CUI: C0265706
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0265706Gastroschisis0self