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Details
Link-It Detail - Disease - Anodontia
Debug Stats
  • ### Total Build Time: 33 ms 23.890 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 316 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 395 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= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 555 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 4.113 KB
  • CONCEPT_RELATIONSHIPS gt=13 ms Completed: 13 ms rowSize= 13.207 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 3.968 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.144 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Anodontia C0399352
Definition (1)
Congenital absence of the teeth; it may involve all (total anodontia) or only some of the teeth (partial anodontia, hypodontia), and both the deciduous and the permanent dentition, or only teeth of the permanent dentition. (Dorland, 27th ed)
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 (50)

Relation Types:
diso_​to_​anat : 6
diso_​to_​chem : 2
diso_​to_​diso : 39
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 19
associated_​with : 2
classifies : 1
expanded_​form_​of : 1
isa : 1
location_​of : 1
mapped_​to : 25
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN94img genetic aspects C0017399
DISO_to_ANAT73img Dens incisivus C0021156
DISO_to_DISO65img Complication Aspects C1171258
DISO_to_PHEN60img genetic aspects C0017399
DISO_to_DISO50img Complication Aspects C1171258
DISO_to_ANAT42img Dens incisivus C0021156
DISO_to_DISO31img Ectodermal Dysplasia C0013575
DISO_to_DISO26img Ectodermal Dysplasia C0013575
DISO_to_ANAT25img Bicuspid C1704302
DISO_to_ANAT20img Bicuspid C1704302
DISO_to_CHEM20img PAX 009 TRANSCRIPTION FACTOR C1571472
DISO_to_PHYS19img Odontogenesis C0028877
DISO_to_DISO17img Cleft Palate C0008925
DISO_to_DISO16img Cleft Palate C0008925
DISO_to_DISO15img Christ-Siemens-Touraine syndrome C0162359
DISO_to_DISO15img Malocclusion C0024636
DISO_to_ANAT14img Maxilla C0024947
DISO_to_CHEM14img TRANSCRIPTION FACTOR C0040648
DISO_to_DISO14img Jaw, Edentulous, Partially C0022367
DISO_to_ANATlocation_ofimg Dentition, Primary C0079214
DISO_to_DISOmapped_toimg ADULT SYNDROME C1863204
DISO_to_DISOmapped_toimg ANODONTIA OF PERMANENT DENTITION C1290511
DISO_to_DISOmapped_toimg Absent teeth C0457756
DISO_to_DISOmapped_toimg Aloi Tomasini Isaia syndrome C2931405
DISO_to_DISOexpanded_form_ofimg Anodontia C0399352
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanEDARADD128178EDAR-associated death domain
img OMIM, Score=1000, UMLKSK CUI: C0399352
HumanEDAR10913ectodysplasin A receptor
img OMIM, Score=1000, UMLKSK CUI: C0399352
HumanPVRL15818poliovirus receptor-related 1 (herpesvirus entry mediator C)
img OMIM, Score=1000, UMLKSK CUI: C0399352
HumanPAX95083paired box 9
img GENERIF, Score=827, Pubmed Id: 14689302, UMLKSK CUI: C0399352
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0399352Anodontia0self