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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:CNS hypomyelination
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Accession:HP:0003429 term browser browse the term
Definition:Reduced amount of myelin in the central nervous system resulting from defective myelinogenesis.
Synonyms:xref: SNOMEDCT_US:111007000;   UMLS:C0544820;   UMLS:C4025616

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  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the nervous system 0
        Abnormal nervous system morphology 0
          Abnormal myelination 0
            Abnormal CNS myelination 0
              CNS hypomyelination 0
                Cerebral hypomyelination 0
                Spinal hypomyelination 0
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