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Details
Link-It Detail - Disease - Dyggve-Melchior-Clausen syndrome
Debug Stats
  • ### Total Build Time: 85 ms 15.227 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 362 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=1 ms Completed: 1 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=66 ms Completed: 66 ms rowSize= 12.288 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 1.349 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Dyggve-Melchior-Clausen syndrome C0265286
Relationships (50)

Relation Types:
diso_​to_​anat : 1
diso_​to_​diso : 49


Relationships:
expanded_​form_​of : 1
manifestation_​of : 49
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATmanifestation_ofimg Kyphosis thoracica C1184919
DISO_to_DISOmanifestation_ofimg Abnormally short neck C0521525
DISO_to_DISOmanifestation_ofimg Adult height 98-127 cm C1857182
DISO_to_DISOmanifestation_ofimg Allelic with Smith-McCort dysplasia (607326) C1857195
DISO_to_DISOmanifestation_ofimg Anterior beaking of vertebral bodies C1846440
DISO_to_DISOmanifestation_ofimg Big jaw C0033324
DISO_to_DISOmanifestation_ofimg Broad chest C1839248
DISO_to_DISOmanifestation_ofimg Broad feet C1866241
DISO_to_DISOmanifestation_ofimg Broad hand C0264142
DISO_to_DISOmanifestation_ofimg C1-C2 dislocation C1857185
DISO_to_DISOmanifestation_ofimg Calvarial thickening (parietal and occipital regions) C1857183
DISO_to_DISOmanifestation_ofimg Caused by mutations in the FLJ90130 gene (FLJ90130, 607461.0001) C1857194
DISO_to_DISOmanifestation_ofimg Coarse facies C0239539
DISO_to_DISOmanifestation_ofimg Cone-shaped epiphyses C1865037
DISO_to_DISOmanifestation_ofimg Congenital Camptodactyly C0685409
DISO_to_DISOmanifestation_ofimg Deformed sella turcica C1846437
DISO_to_DISOexpanded_form_ofimg Dyggve-Melchior-Clausen syndrome C0265286
DISO_to_DISOmanifestation_ofimg Flared acromion C1857181
DISO_to_DISOmanifestation_ofimg Flat acetabular roof C1837485
DISO_to_DISOmanifestation_ofimg Flat glenoid fossa C1855177
DISO_to_DISOmanifestation_ofimg Genu valga ICD10CM:M21.06 C3276330
DISO_to_DISOmanifestation_ofimg Growth retardation, postnatal C1865007
DISO_to_DISOmanifestation_ofimg Hyperpneumatization of paranasal sinuses C1857184
DISO_to_DISOmanifestation_ofimg Hypoplastic facial bones C1846438
DISO_to_DISOmanifestation_ofimg Hypoplastic odontoid process C1854976
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanDYM54808dymeclin
img OMIM, Score=1000, UMLKSK CUI: C0265286
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0265286Dyggve-Melchior-Clausen syndrome0self