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Details
Link-It Detail - Disease - Fibromatosis, Gingival
Debug Stats
  • ### Total Build Time: 18 ms 22.293 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 577 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
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 992 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 5.383 KB
  • CONCEPT_RELATIONSHIPS gt=9 ms Completed: 9 ms rowSize= 9.994 KB
  • CONCEPT_GENES gt=3 ms Completed: 3 ms rowSize= 3.621 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.156 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Disease (2)
Fibromatosis, Gingival C0016049
Fibromatoses, Gingival
Definition (1)
Generalized or localized diffuse fibrous overgrowth of the gingival tissue, usually transmitted as an autosomal dominant trait, but some cases are idiopathic and others produced by drugs. The enlarged gingiva is pink, firm, and has a leather-like consistency with a minutely pebbled surface and in severe cases the teeth are almost completely covered and the enlargement projects into the oral vestibule. (Dorland, 28th ed)
Semantic Types (1)
Congenital Abnormality (T019)
Parents (2)
img Gingival Overgrowth C0376480
img Mouth Abnormalities C0026633
Ancestral Roots
RootRoot Plus OneDepthParent
img Stomatognathic Diseases C0038368img Mouth Diseases C00266366img Gingival Overgrowth C0376480
img Stomatognathic Diseases C0038368img Stomatognathic System Abnormalities C02430574img Mouth Abnormalities C0026633
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007685img Mouth Abnormalities C0026633
img Stomatognathic Diseases C0038368img Mouth Diseases C00266364img Mouth Abnormalities C0026633
Relationships (22)

Relation Types:
diso_​to_​anat : 6
diso_​to_​chem : 1
diso_​to_​diso : 13
diso_​to_​phen : 2


Relationships:
none : 12
associated_​with : 1
isa : 3
location_​of : 1
mapped_​to : 4
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN25img genetic aspects C0017399
DISO_to_PHEN23img genetic aspects C0017399
DISO_to_DISO10img Complication Aspects C1171258
DISO_to_ANAT9img Gingiva C0017562
DISO_to_DISO8img Complication Aspects C1171258
DISO_to_ANAT6img Fibroblasts C0016030
DISO_to_DISO5img Abnormalities, Multiple C0000772
DISO_to_ANAT4img Fibroblasts C0016030
DISO_to_ANAT4img Gingiva C0017562
DISO_to_ANAT4img Hyalin C0020191
DISO_to_CHEM4img SON OF SEVENLESS HOMOLOG A 001 C0217396
DISO_to_DISO4img Abnormalities, Multiple C0000772
DISO_to_ANATlocation_ofimg Gingiva C0017562
DISO_to_DISOmapped_toimg CHERUBISM, GINGIVAL FIBROMATOSIS, EPILEPSY, MENTAL DEFICIENCY, HYPERTRICHOSIS, AND STUNTED GROWTH C0796133
DISO_to_DISOmapped_toimg FIBROMATOSIS, GINGIVAL, HEREDITARY, 3 C1864960
DISO_to_DISOmapped_toimg FIBROMATOSIS, GINGIVAL, WITH ABNORMAL FINGERS, FINGERNAILS, NOSE AND EARS, AND SPLENOMEGALY C0796013
DISO_to_DISOmapped_toimg FIBROMATOSIS, GINGIVAL, WITH PROGRESSIVE DEAFNESS C1851112
DISO_to_DISOassociated_withimg Fibromatoses C0016048
DISO_to_DISOpermuted_term_ofimg Fibromatoses, Gingival C0016049
DISO_to_DISOisaimg Hereditary gingival fibromatosis C0399440
DISO_to_DISOisaimg Idiopathic gingival fibromatosis C0545059
DISO_to_DISOisaimg Oculocerebral syndrome with hypopigmentation C0268496
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanANTXR2118429anthrax toxin receptor 2
img OMIM, Score=1000, UMLKSK CUI: C0016049
img OMIM, Score=1000, UMLKSK CUI: C0016049
HumanGINGF264644gingival fibromatosis, hereditary, 2
img OMIM, Score=1000, UMLKSK CUI: C0016049
HumanSOS16654son of sevenless homolog 1 (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0016049
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0016049Fibromatosis, Gingival0self