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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:Cranial nerve motor loss
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Accession:HP:0007097 term browser browse the term
Synonyms:xref: UMLS:C4024940



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Cranial nerve motor loss term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G SLC52A3 solute carrier family 52 member 3 IAGP HPO MIM:211530 NCBI chr20:760,080...780,033
Ensembl chr20:760,080...776,015
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Term paths to the root
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Term Annotations click to browse term
  Human phenotype 87531
    Phenotypic abnormality 87110
      Abnormality of the nervous system 29594
        Abnormal nervous system morphology 5495
          Abnormal peripheral nervous system morphology 467
            Abnormal cranial nerve morphology 79
              Cranial nerve motor loss 1
paths to the root