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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:Corticospinal tract hypoplasia
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Accession:HP:0007016 term browser browse the term
Synonyms:xref: UMLS:C1844007



show annotations for term's descendants           Sort by:
Corticospinal tract hypoplasia term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G L1CAM L1 cell adhesion molecule IAGP HPO MIM:307000 NCBI chr  X:153,861,514...153,886,173
Ensembl chr  X:153,861,514...153,886,173
JBrowse link
G PDHB pyruvate dehydrogenase E1 subunit beta IAGP HPO ORPHA:255138 NCBI chr 3:58,427,630...58,433,832
Ensembl chr 3:58,427,630...58,433,857
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  Human phenotype 73897
    Phenotypic abnormality 73592
      Abnormality of the nervous system 28560
        Abnormal nervous system morphology 5270
          Morphological central nervous system abnormality 5155
            Aplasia/Hypoplasia involving the central nervous system 2113
              Aplasia/Hypoplasia involving the corticospinal tracts 2
                Corticospinal tract hypoplasia 2
Path 2
Term Annotations click to browse term
  Human phenotype 73897
    Phenotypic abnormality 73592
      Abnormality of the nervous system 28560
        Abnormal nervous system morphology 5270
          Morphological central nervous system abnormality 5155
            Abnormal pyramidal tract morphology 70
              Abnormal corticospinal tract morphology 50
                Aplasia/Hypoplasia involving the corticospinal tracts 2
                  Corticospinal tract hypoplasia 2
paths to the root