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Details
Link-It Detail - Disease - Congenital malrotation of intestine
Debug Stats
  • ### Total Build Time: 16 ms 18.591 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 368 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 275 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=13 ms Completed: 13 ms rowSize= 12.898 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 3.825 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Congenital malrotation of intestine C0221210
Definition (1)
A congenital abnormality in which the intestine is abnormally rotated (twisted). It may result in intestinal obstruction.
Relationships (41)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 39


Relationships:
associated_​with : 13
is_​associated_​anatomic_​site_​of : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 18
manifestation_​of : 8
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Digestive System C0012240
DISO_to_ANATis_associated_anatomic_site_ofimg Intestines C0021853
DISO_to_DISOmanifestation_ofimg Abdominal distention and pain C2749840
DISO_to_DISOmanifestation_ofimg Atresia of ascending colon C2749842
DISO_to_DISOassociated_withimg Congenital clubbed paw C0685356
DISO_to_DISOisaimg Congenital dextrorotation C0332958
DISO_to_DISOassociated_withimg Congenital duodenal obstruction due to malrotation of intestine C0266184
DISO_to_DISOisaimg Congenital hyperrotation C0332953
DISO_to_DISOisaimg Congenital levorotation C0332959
DISO_to_DISOassociated_withimg Congenital malrotation of claw C0685766
DISO_to_DISOmanifestation_ofimg Congenital malrotation of intestine C0221210
DISO_to_DISOassociated_withimg Congenital malrotation of limb C0685343
DISO_to_DISOassociated_withimg Congenital malrotation of paw C0685353
DISO_to_DISOassociated_withimg Congenital mesenteroaxial volvulus of stomach C0266158
DISO_to_DISOisaimg Congenital non-rotation C0302299
DISO_to_DISOassociated_withimg Congenital organoaxial volvulus of stomach C0266157
DISO_to_DISOisaimg Congenital turning downward C0332957
DISO_to_DISOisaimg Congenital turning inward C0332955
DISO_to_DISOisaimg Congenital turning outward C0332954
DISO_to_DISOisaimg Congenital turning upward C0332956
DISO_to_DISOisaimg Congenital volvulus C0345252
DISO_to_DISOassociated_withimg Congenital volvulus of stomach C0266156
DISO_to_DISOmanifestation_ofimg Constipation C0009806
DISO_to_DISOisaimg Familial intestinal malrotation C0345255
DISO_to_DISOassociated_withimg Incomplete fixation of caecum C0266193
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanPORCN64840porcupine homolog (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0221210
HumanMKS154903Meckel syndrome, type 1
img OMIM, Score=1000, UMLKSK CUI: C0221210
HumanLRP24036low density lipoprotein receptor-related protein 2
img OMIM, Score=1000, UMLKSK CUI: C0221210
HumanGPC32719glypican 3
img OMIM, Score=1000, UMLKSK CUI: C0221210
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0221210Congenital malrotation of intestine0self