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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 involving the corticospinal tracts
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Accession:HP:0007365 term browser browse the term
Synonyms:xref: UMLS:C4024901


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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 74032
    Phenotypic abnormality 73727
      Abnormality of the nervous system 28579
        Abnormal nervous system morphology 5274
          Morphological central nervous system abnormality 5159
            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 74032
    Phenotypic abnormality 73727
      Abnormality of the nervous system 28579
        Abnormal nervous system morphology 5274
          Morphological central nervous system abnormality 5159
            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