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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:Agammaglobulinemia
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Accession:HP:0004432 term browser browse the term
Definition:A lasting absence of total IgG and total IgA and total IgM in the blood circulation, whereby at most trace quantities can be measured.
Synonyms:exact_synonym: Agammaglobulinaemia
 alt_id: HP:0008328
 xref: MESH:D000361;   SNOMEDCT_US:119249001;   UMLS:C0001768


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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 immune system 0
        Abnormality of immune system physiology 0
          Abnormality of humoral immunity 0
            Abnormal immunoglobulin level 0
              Decreased circulating antibody level 0
                Agammaglobulinemia 0
Path 2
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the immune system 0
        Abnormality of immune system physiology 0
          Abnormal leukocyte physiology 0
            Abnormal lymphocyte physiology 0
              Abnormality of B cell physiology 0
                Abnormal immunoglobulin level 0
                  Decreased circulating antibody level 0
                    Agammaglobulinemia 0
paths to the root