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The Human Phenotype Ontology (HPO) is downloaded weekly from The file downloaded is considered the "last stable build" available for the ontology. For more about the HPO, view their website at

Term:Diffuse cerebral sclerosis
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Accession:HP:0006918 term browser browse the term
Synonyms:xref: MESH:D002549;   SNOMEDCT_US:49692006;   UMLS:C0007795

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Diffuse cerebral sclerosis term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G AIMP1 aminoacyl tRNA synthetase complex interacting multifunctional protein 1 IAGP HPO NCBI chr 4:106,315,544...106,349,456
Ensembl chr 4:106,315,544...106,349,456
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Term paths to the root
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Term Annotations click to browse term
  Human phenotype 16463
    Phenotypic abnormality 16461
      Abnormality of the nervous system 11458
        Abnormal nervous system morphology 4266
          Morphological central nervous system abnormality 4119
            Abnormality of brain morphology 3056
              Abnormal forebrain morphology 2166
                Abnormal cerebral morphology 2139
                  Diffuse cerebral sclerosis 1
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