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Details
Link-It Detail - Disease - Poland Syndrome
Debug Stats
  • ### Total Build Time: 49 ms 19.520 KB
  • CONCEPT_NAME gt=16 ms Completed: 16 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 383 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=5 ms Completed: 5 ms rowSize= 546 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 4.082 KB
  • CONCEPT_RELATIONSHIPS gt=18 ms Completed: 18 ms rowSize= 12.740 KB
  • CONCEPT_GENES gt=1 ms Completed: 1 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Poland Syndrome C0032357
Definition (1)
A rare developmental disorder characterized by underdevelopment or absence of the pectoralis muscle in one side of the chest, usually associated with ipsilateral cutaneous syndactyly, and ipsilateral breast and nipple hypoplasia.
Semantic Types (2)
Disease or Syndrome (T047)
Congenital Abnormality (T019)
Parents (1)
img Syndactyly C0039075
Ancestral Roots
RootRoot Plus OneDepthParent
img Musculoskeletal Diseases C0026857img Bone Diseases C00059407img Syndactyly C0039075
img Musculoskeletal Diseases C0026857img Musculoskeletal Abnormalities C01514915img Syndactyly C0039075
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007686img Syndactyly C0039075
Relationships (34)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 31
diso_​to_​phen : 1


Relationships:
none : 7
alias_​of : 1
manifestation_​of : 25
related_​to : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO25img Complication Aspects C1171258
DISO_to_DISO23img Complication Aspects C1171258
DISO_to_ANAT11img Breast C0006141
DISO_to_ANAT10img Chest wall structure C0205076
DISO_to_DISO7img DEXTROCARDIA C0011813
DISO_to_DISO7img Mobius Syndrome C0221060
DISO_to_PHEN7img genetic aspects C0017399
DISO_to_DISOmanifestation_ofimg Absence of pectoralis minor muscle C1868158
DISO_to_DISOmanifestation_ofimg All features are unilateral C1868172
DISO_to_DISOmanifestation_ofimg Congenital hemivertebra C0265677
DISO_to_DISOmanifestation_ofimg Deltoid muscle hypoplasia C1868170
DISO_to_DISOmanifestation_ofimg Dextrocardia (in left-sided Poland sequence) C1868171
DISO_to_DISOmanifestation_ofimg Fused ribs C1844749
DISO_to_DISOmanifestation_ofimg Hypoplasia of infraspinatus muscle C1868168
DISO_to_DISOmanifestation_ofimg Hypoplasia of latissimus dorsi muscle C1868166
DISO_to_DISOmanifestation_ofimg Hypoplasia of serratus anterior muscle C1868167
DISO_to_DISOmanifestation_ofimg Hypoplasia of supraspinatus muscle C1868169
DISO_to_DISOmanifestation_ofimg Hypoplastic ribs C1868159
DISO_to_DISOmanifestation_ofimg Majority cases are sporadic C1867119
DISO_to_DISOmanifestation_ofimg Occurs on right side in 75% of cases C1868173
DISO_to_DISOrelated_toimg PECTORALIS MUSCLE, ABSENCE OF C1868156
DISO_to_DISOmanifestation_ofimg Pedigrees compatible with autosomal dominant inheritance have been reported C1868175
DISO_to_DISOalias_ofimg Poland Syndrome C0032357
DISO_to_DISOmanifestation_ofimg Poland syndrome can be associated with Moebius syndrome (157900) C1868176
DISO_to_DISOmanifestation_ofimg Sprengel anomaly C1860355
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0032357Poland Syndrome0self