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Details
Link-It Detail - Disease - Prune Belly Syndrome
Debug Stats
  • ### Total Build Time: 187 ms 17.944 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 338 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 359 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=1 ms Completed: 1 ms rowSize= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=15 ms Completed: 15 ms rowSize= 559 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.557 KB
  • CONCEPT_RELATIONSHIPS gt=158 ms Completed: 158 ms rowSize= 13.741 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Prune Belly Syndrome C0033770
Definition (1)
A syndrome characterized by abdominal wall musculature deficiency, cryptorchism, and urinary tract abnormalities. The syndrome derives its name from its characteristic distended abdomen with wrinkled skin.
Semantic Types (1)
Congenital Abnormality (T019)
Parents (1)
img Abnormalities, Multiple C0000772
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007684img Abnormalities, Multiple C0000772
Relationships (42)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 1
diso_​to_​diso : 36
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 7
associated_​with : 1
classifies : 2
isa : 2
location_​of : 1
manifestation_​of : 24
mapped_​to : 4
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO19img Complication Aspects C1171258
DISO_to_DISO13img Complication Aspects C1171258
DISO_to_PHEN10img genetic aspects C0017399
DISO_to_ANAT5img Urinary Bladder C0005682
DISO_to_CHEM4img Hepatocyte Nuclear Factor 1-beta C0126037
DISO_to_ANAT3img Urethra C0041967
DISO_to_PHYS3img Mutation C0026882
DISO_to_ANATlocation_ofimg Rectus Abdominis C0206066
DISO_to_DISOmanifestation_ofimg (Dry mouth) or (salivary hyposecretion) C0043352
DISO_to_DISOmanifestation_ofimg ANAL IMPERFORATION C0003466
DISO_to_DISOmanifestation_ofimg Absent abdominal musculature C3149223
DISO_to_DISOclassifiesimg All other congenital anomalies C0810365
DISO_to_DISOmanifestation_ofimg Anus, Imperforate C0003466
DISO_to_DISOmanifestation_ofimg Bladder distention C0005687
DISO_to_DISOmanifestation_ofimg Caused by mutation in the muscarinic cholinergic receptor-3 gene (CHRM3, 118494.0001) C3276091
DISO_to_DISOmanifestation_ofimg Clubfoot C0009081
DISO_to_DISOmanifestation_ofimg Congenital Heart Defects C0018798
DISO_to_DISOassociated_withimg Congenital absence C0332907
DISO_to_DISOmanifestation_ofimg Congenital funnel chest C0016842
DISO_to_DISOmanifestation_ofimg Congenital pectus carinatum C0158731
DISO_to_DISOmanifestation_ofimg Congenital posterior urethral valve C0238506
DISO_to_DISOmapped_toimg Congenital prolapse of bladder C0266341
DISO_to_DISOmapped_toimg Congenital prolapse of bladder mucosa C0345342
DISO_to_DISOmanifestation_ofimg Cryptorchidism C0010417
DISO_to_DISOmanifestation_ofimg Dilatation of ureter C0521620
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0033770Prune Belly Syndrome0self