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Details
Link-It Detail - Disease - SMITH-MCCORT DYSPLASIA
Debug Stats
  • ### Total Build Time: 7 ms 14.946 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 342 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=5 ms Completed: 5 ms rowSize= 12.048 KB
  • CONCEPT_GENES gt=1 ms Completed: 1 ms rowSize= 1.338 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.156 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
SMITH-MCCORT DYSPLASIA C1846431
Relationships (33)

Relation Types:
diso_​to_​diso : 33


Relationships:
expanded_​form_​of : 1
manifestation_​of : 32
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmanifestation_ofimg Allelic to Dyggve-Melchior-Clausen disease (223800) C2675922
DISO_to_DISOmanifestation_ofimg Anterior beaking of vertebral bodies C1846440
DISO_to_DISOmanifestation_ofimg Atlantoaxial instability C0410653
DISO_to_DISOmanifestation_ofimg Average intellect C0423900
DISO_to_DISOmanifestation_ofimg Caused by mutations in the FLJ90140 gene (FLJ90130, 607461.0005) C1846450
DISO_to_DISOmanifestation_ofimg DOLICHOCEPHALY C0221358
DISO_to_DISOmanifestation_ofimg Deformed sella turcica C1846437
DISO_to_DISOmanifestation_ofimg Delayed femoral head ossification C1846446
DISO_to_DISOmanifestation_ofimg Genu Varum C0544755
DISO_to_DISOmanifestation_ofimg Genu valga ICD10CM:M21.06 C3276330
DISO_to_DISOmanifestation_ofimg Hypoplastic acetabulae C1846442
DISO_to_DISOmanifestation_ofimg Hypoplastic facial bones C1846438
DISO_to_DISOmanifestation_ofimg Irregular epiphyses C1846449
DISO_to_DISOmanifestation_ofimg Irregular metaphyses C1846448
DISO_to_DISOmanifestation_ofimg Kyphosis C0022821
DISO_to_DISOmanifestation_ofimg Lacy iliac crest C1846441
DISO_to_DISOmanifestation_ofimg MICROCEPHALY C0025958
DISO_to_DISOmanifestation_ofimg Multicentric femoral head ossification C1846447
DISO_to_DISOmanifestation_ofimg ODONTOID HYPOPLASIA C1846439
DISO_to_DISOmanifestation_ofimg Platyspondyly C1865023
DISO_to_DISOexpanded_form_ofimg SMITH-MCCORT DYSPLASIA C1846431
DISO_to_DISOmanifestation_ofimg Scoliosis C0036439
DISO_to_DISOmanifestation_ofimg Short barrel-shaped chest C1846432
DISO_to_DISOmanifestation_ofimg Short ischia C1846443
DISO_to_DISOmanifestation_ofimg Short metacarpals C1837084
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanDYM54808dymeclin
img OMIM, Score=1000, UMLKSK CUI: C1846431
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1846431SMITH-MCCORT DYSPLASIA0self