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Details
Link-It Detail - Disease - Marshall syndrome
Debug Stats
  • ### Total Build Time: 77 ms 16.728 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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=69 ms Completed: 69 ms rowSize= 12.040 KB
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 3.142 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Marshall syndrome C0265235
Relationships (37)

Relation Types:
diso_​to_​anat : 1
diso_​to_​diso : 36


Relationships:
manifestation_​of : 37
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATmanifestation_ofimg Palpebronasal fold C0229249
DISO_to_DISOmanifestation_ofimg Absent frontal sinuses C1849544
DISO_to_DISOmanifestation_ofimg Anteverted nares C1853244
DISO_to_DISOmanifestation_ofimg Calvarial thickening C1849519
DISO_to_DISOmanifestation_ofimg Cataracts, congenital ICD10CM:Q12.0 C3275988
DISO_to_DISOmanifestation_ofimg Caused by mutation in the collagen XI, alpha-1 polypeptide gene (COL11A1, 120280.0002) C1835102
DISO_to_DISOmanifestation_ofimg Cleft Palate C0008925
DISO_to_DISOmanifestation_ofimg Congenital micrognathia C0025990
DISO_to_DISOmanifestation_ofimg Coxa valga C0239137
DISO_to_DISOmanifestation_ofimg Esotropia C0014877
DISO_to_DISOmanifestation_ofimg Falx, tentorial, and meningeal calcifications C1835096
DISO_to_DISOmanifestation_ofimg Flat midface C1858085
DISO_to_DISOmanifestation_ofimg Flat nasal bridge C1837403
DISO_to_DISOmanifestation_ofimg Glaucoma C0017601
DISO_to_DISOmanifestation_ofimg Hearing Loss, Sensorineural C0018784
DISO_to_DISOmanifestation_ofimg Hypertelorism C0020534
DISO_to_DISOmanifestation_ofimg Lens dislocation C0023309
DISO_to_DISOmanifestation_ofimg Long philtrum C1865014
DISO_to_DISOmanifestation_ofimg Low set ears ICD10CM:Q17.4 C3276227
DISO_to_DISOmanifestation_ofimg Marshall syndrome is allelic to Stickler syndrome, type 2 (604841) C2675051
DISO_to_DISOmanifestation_ofimg Micrognathism C0025990
DISO_to_DISOmanifestation_ofimg Mild platyspondyly C1848999
DISO_to_DISOmanifestation_ofimg Myopia C0027092
DISO_to_DISOmanifestation_ofimg Outward radial bowing C1835099
DISO_to_DISOmanifestation_ofimg Outward ulnar bowing C1835100
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanCOL11A11301collagen, type XI, alpha 1
img OMIM, Score=1000, UMLKSK CUI: C0265235
img OMIM, Score=1000, UMLKSK CUI: C0265235
img OMIM, Score=1000, UMLKSK CUI: C0265235
img GENERIF, Score=983, Pubmed Id: 17236192, UMLKSK CUI: C0265235
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0265235Marshall syndrome0self