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ONTOLOGY REPORT - ANNOTATIONS


Term:Partington Anderson Syndrome
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Accession:DOID:9004591 term browser browse the term
Synonyms:primary_id: MESH:C536299;   RDO:0001825
For additional species annotation, visit the Alliance of Genome Resources.


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Path 1
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  disease 15609
    syndrome 5791
      Partington Anderson Syndrome 0
Path 2
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  disease 15609
    Developmental Diseases 8986
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7802
        genetic disease 7293
          monogenic disease 4988
            autosomal genetic disease 3968
              autosomal dominant disease 2417
                complex cortical dysplasia with other brain malformations 503
                  Malformations of Cortical Development, Group I 357
                    microcephaly 226
                      Partington Anderson Syndrome 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.