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Details
Link-It Detail - Disease - Ectromelia
Debug Stats
  • ### Total Build Time: 28 ms 17.905 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 318 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 244 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=4 ms Completed: 4 ms rowSize= 564 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.855 KB
  • CONCEPT_RELATIONSHIPS gt=19 ms Completed: 19 ms rowSize= 12.540 KB
  • CONCEPT_GENES gt=1 ms Completed: 1 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.145 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Ectromelia C0013589
Definition (1)
A congenital defect characterized by the absence or hypoplasia of one or more extremities.
Semantic Types (1)
Congenital Abnormality (T019)
Parents (1)
img Limb Deformities, Congenital C0206762
Ancestral Roots
RootRoot Plus OneDepthParent
img Musculoskeletal Diseases C0026857img Musculoskeletal Abnormalities C01514914img Limb Deformities, Congenital C0206762
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007685img Limb Deformities, Congenital C0206762
Relationships (45)

Relation Types:
diso_​to_​anat : 7
diso_​to_​diso : 36
diso_​to_​phen : 2


Relationships:
none : 16
associated_​with : 2
isa : 4
location_​of : 2
mapped_​to : 21
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN32img genetic aspects C0017399
DISO_to_DISO27img Abnormalities, Multiple C0000772
DISO_to_DISO25img Abnormalities, Multiple C0000772
DISO_to_PHEN21img genetic aspects C0017399
DISO_to_DISO18img Complication Aspects C1171258
DISO_to_ANAT16img Fibula C0016068
DISO_to_ANAT12img Fibula C0016068
DISO_to_DISO11img Complication Aspects C1171258
DISO_to_ANAT8img Bone structure of tibia C0040184
DISO_to_DISO8img Congenital Hand Deformities C0018566
DISO_to_ANAT7img Bone structure of radius C0034627
DISO_to_DISO7img Abnormalities, Craniofacial C0376634
DISO_to_DISO6img chemically induced C0007994
DISO_to_ANAT5img Femur C0015811
DISO_to_DISO5img 4-13 CONGENITAL ANOMALIES OF THE UPPER LIMB C0749794
DISO_to_DISO5img Hypertelorism C0020534
DISO_to_ANATlocation_ofimg Extremities C0015385
DISO_to_ANATlocation_ofimg Structure of long bone C0222647
DISO_to_DISOmapped_toimg AARRS C1848651
DISO_to_DISOmapped_toimg ABSENCE OF LIMBS C0541755
DISO_to_DISOmapped_toimg ACLH C1832434
DISO_to_DISOisaimg AMELIA C0002447
DISO_to_DISOmapped_toimg APHALANGY WITH HEMIVERTEBRAE C1859754
DISO_to_DISOassociated_withimg Abnormally short growth C0332895
DISO_to_DISOmapped_toimg Absence of all four limbs with ectodermal dysplasia and lacrimal duct abnormalities C2931214
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0013589Ectromelia0self