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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:Oculopalatocerebral Syndrome
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Accession:DOID:9000698 term browser browse the term
Synonyms:exact_synonym: OPC DWARFISM;   Oculopalatocerebral Dwarfism
 primary_id: MESH:C564935;   RDO:0013727
 alt_id: OMIM:257910


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 41189
    syndrome 18075
      Oculopalatocerebral Syndrome 0
Path 2
Term Annotations click to browse term
  disease 41189
    Developmental Disease 36464
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 33606
        genetic disease 33187
          monogenic disease 18511
            autosomal genetic disease 16781
              autosomal dominant disease 10884
                complex cortical dysplasia with other brain malformations 2173
                  Malformations of Cortical Development, Group I 1862
                    microcephaly 1521
                      Oculopalatocerebral Syndrome 0
paths to the root