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HUMAN PHENOTYPE - ANNOTATIONS

The Human Phenotype Ontology (HPO) is downloaded weekly from http://compbio.charite.de/hudson/job/hpo/lastStableBuild/artifact/ontology/release/hp.obo. The file downloaded is considered the "last stable build" available for the ontology. For more about the HPO, view their website at http://www.human-phenotype-ontology.org/.

Term:Gingival fibromatosis
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Accession:HP:0000169 term browser browse the term
Definition:The presence of fibrosis of the gingiva.
Comment:Gingival fibromatosis is characterized by a slowly progressive benign enlargement of the oral gingival tissues. Both genetic and pharmacologically induced forms of gingival fibromatosis are known. The most common genetic form, hereditary gingival fibromatosis (HGF), is usually transmitted as an autosomal dominant trait, although sporadic cases are common and autosomal recessive inheritance has been reported.
Synonyms:exact_synonym: Gingival fibroma;   Gingival fibrous nodules
 narrow_synonym: Hereditary gingival fibromatosis;   Idiopathic gingival hyperplasia
 xref: MESH:C562884;   MESH:D005351;   NCI:C3041;   SNOMEDCT_US:109620006;   SNOMEDCT_US:58569000;   UMLS:C0016049;   UMLS:C0399440;   UMLS:C4280677



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Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Neoplasm 0
        Neoplasm by histology 0
          Fibrous tissue neoplasm 0
            Fibroma 0
              Gingival fibromatosis 0
Path 2
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of head or neck 0
        Abnormality of the head 0
          Abnormality of the face 0
            Abnormality of the mouth 0
              Abnormal oral morphology 0
                Abnormal oral cavity morphology 0
                  Abnormal oral mucosa morphology 0
                    Abnormality of the gingiva 0
                      Gingival fibromatosis 0
paths to the root