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Details
Link-It Detail - Disease - Dentin Dysplasia
Debug Stats
  • ### Total Build Time: 85 ms 14.731 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 401 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= 247 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=16 ms Completed: 16 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=30 ms Completed: 30 ms rowSize= 4.113 KB
  • CONCEPT_RELATIONSHIPS gt=18 ms Completed: 18 ms rowSize= 5.223 KB
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 2.713 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Disease (1)
Dentin Dysplasia C0011430
Definition (1)
An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed)
Semantic Types (2)
Congenital Abnormality (T019)
Disease or Syndrome (T047)
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 (9)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 1
diso_​to_​diso : 5
diso_​to_​phen : 1


Relationships:
none : 3
associated_​with : 1
location_​of : 2
mapped_​to : 2
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN14img genetic aspects C0017399
DISO_to_CHEM9img Extracellular Matrix Protein C0079323
DISO_to_DISO9img Dentinogenesis Imperfecta C0011436
DISO_to_ANATlocation_ofimg Dentin C0011429
DISO_to_ANATlocation_ofimg Dentition, Primary C0079214
DISO_to_DISOassociated_withimg Congenital dysplasia C0332865
DISO_to_DISOmapped_toimg DENTIN DYSPLASIA, SHIELDS TYPE I C0399379
DISO_to_DISOpermuted_term_ofimg Dentin Dysplasia C0011430
DISO_to_DISOmapped_toimg Dentin dysplasia sclerotic bones C1852201
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanDSPP1834dentin sialophosphoprotein
img OMIM, Score=1000, UMLKSK CUI: C0011430
img GENERIF, Score=901, Pubmed Id: 18521831, UMLKSK CUI: C0011430
img OMIM, Score=1000, UMLKSK CUI: C0011430
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0011430Dentin Dysplasia0self