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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:Thyroid dysgenesis
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Accession:HP:0008188 term browser browse the term
Definition:Thyroid dysgenesis is a descriptive term that should be avoided if more precise information is available. However, the HPO keeps retains this term because it is commonly used in the medical literature. In humans, the process of thyroid morphogenesis occurs from the 3rd to 16th week of gestation. Alterations occurring during this period may result in a thyroid gland that is absent (thyroid agenesis or athyreosis), hypoplastic (thyroid hypoplasia), or located in an unusual position (thyroid ectopy). All these entities are grouped under the term thyroid dysgenesis.
Synonyms:exact_synonym: Thyroid dysplasia
 xref: UMLS:C1563716


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  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the endocrine system 0
        Abnormality of the thyroid gland 0
          Abnormal thyroid morphology 0
            Thyroid dysgenesis 0
              Ectopic thyroid + 0
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