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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:Amelogenesis imperfecta
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Accession:HP:0000705 term browser browse the term
Definition:A developmental dysplasia of the dental enamel.
Comment:Amelogenesis imperfecta (AI) is a term for a clinically and genetically heterogeneous group of diseases that affect the dental enamel, occasionally in conjunction with other dental, oral and extraoral tissues. This term has often been used to describe the phenotype associated with AI, but for new annotations it is recommended to describe the individual manifestations.
Synonyms:alt_id: HP:0006284;   HP:0006310;   HP:0006325;   HP:0006327;   HP:0006331
 xref: SNOMEDCT_US:78494001;   UMLS:C0002452


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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
            Abnormal dental enamel morphology 0
              Amelogenesis imperfecta 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 dental enamel morphology 0
                        Amelogenesis imperfecta 0
paths to the root