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Details
Link-It Detail - Disease - Odontodysplasia
Debug Stats
  • ### Total Build Time: 122 ms 14.154 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 569 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=13 ms Completed: 13 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.113 KB
  • CONCEPT_RELATIONSHIPS gt=85 ms Completed: 85 ms rowSize= 7.208 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Odontodysplasia C0206554
Definition (1)
A localized arrested tooth development which appears to involve most commonly the anterior teeth, usually on one side of the midline, most often the maxillary central and lateral incisors. Roentgenographically, the teeth have a ghostlike appearance. Calcification and bits of prismatic enamel may be found in the pulp and the enamel is thin and absent in part. (Jablonski, Illustrated Dictionary of Dentistry, 1982)
Semantic Types (1)
Congenital Abnormality (T019)
Parents (1)
img Tooth Abnormalities C0040427
Ancestral Roots
RootRoot Plus OneDepthParent
img Stomatognathic Diseases C0038368img Tooth Diseases C00404354img Tooth Abnormalities C0040427
img Stomatognathic Diseases C0038368img Stomatognathic System Abnormalities C02430574img Tooth Abnormalities C0040427
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007685img Tooth Abnormalities C0040427
Relationships (15)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 1
diso_​to_​diso : 10
diso_​to_​phen : 1


Relationships:
none : 9
associated_​with : 1
location_​of : 1
mapped_​to : 3
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO6img Complication Aspects C1171258
DISO_to_PHEN5img genetic aspects C0017399
DISO_to_DISO4img Abnormalities, Multiple C0000772
DISO_to_ANAT3img Deciduous tooth C3266841
DISO_to_ANAT3img Maxilla C0024947
DISO_to_CHEM3img Connexin 43 C0110613
DISO_to_DISO3img Abnormalities, Eye C0015393
DISO_to_DISO3img BONE DEVELOPMENT DISORDER C0005941
DISO_to_DISO3img Disease, Maxillary C0024950
DISO_to_ANATlocation_ofimg Tooth C0040426
DISO_to_DISOassociated_withimg Congenital dysplasia C0332865
DISO_to_DISOmapped_toimg Merten-Singleton syndrome C0432254
DISO_to_DISOmapped_toimg OODD C0796093
DISO_to_DISOpermuted_term_ofimg Odontodysplasia C0206554
DISO_to_DISOmapped_toimg TRICHODENTAL DYSPLASIA C0406724
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0206554Odontodysplasia0self