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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:Aplasia/Hypoplasia of the cerebellum
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Accession:HP:0007360 term browser browse the term
Synonyms:exact_synonym: Absent/small cerebellum;   Absent/underdeveloped cerebellum;   Atrophy/Degeneration affecting the cerebellum;   Atrophy/Hypoplasia of the cerebellum;   Cerebellar hypoplasia/atrophy
 alt_id: HP:0006857;   HP:0007368
 xref: UMLS:C3279222



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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 nervous system 0
        Abnormal nervous system morphology 0
          Morphological central nervous system abnormality 0
            Aplasia/Hypoplasia involving the central nervous system 0
              Aplasia/Hypoplasia of the cerebellum 0
                Aplasia/Hypoplasia of the cerebellar vermis + 0
                Cerebellar agenesis 0
                Cerebellar hypoplasia + 0
Path 2
Term Annotations click to browse term
  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the nervous system 0
        Abnormal nervous system morphology 0
          Morphological central nervous system abnormality 0
            Abnormality of brain morphology 0
              Abnormal hindbrain morphology 0
                Abnormal metencephalon morphology 0
                  Abnormal cerebellum morphology 0
                    Aplasia/Hypoplasia of the cerebellum 0
                      Aplasia/Hypoplasia of the cerebellar vermis + 0
                      Cerebellar agenesis 0
                      Cerebellar hypoplasia + 0
paths to the root