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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:Dentinogenesis imperfecta limited to primary teeth
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Accession:HP:0011060 term browser browse the term
Definition:Developmental dysplasia of dentin affecting only the primary dentition.
Synonyms:exact_synonym: Dentinogenesis imperfecta of baby teeth
 xref: MESH:D003805;   SNOMEDCT_US:109492001;   UMLS:C0011430;   UMLS:C4023558



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Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the musculoskeletal system 0
        Abnormality of the skeletal system 0
          Abnormal odontoid tissue morphology 0
            Dentinogenesis imperfecta 0
              Dentinogenesis imperfecta limited to primary teeth 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
                  Abnormality of the dentition 0
                    Abnormality of dental structure 0
                      Abnormal dentin morphology 0
                        Dentinogenesis imperfecta 0
                          Dentinogenesis imperfecta limited to primary teeth 0
paths to the root