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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:ocular motor apraxia, Cogan type
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Accession:DOID:0080849 term browser browse the term
Definition:An eye disease that is characterized by defective or absent horizontal voluntary eye movements, and defective or absent horizontal ocular attraction movements. (DO)
Synonyms:exact_synonym: COMA;   Cogan's syndrome, type 2;   Ocular Motor Apraxia;   Oculomotor Apraxia, Cogan Type;   congenital oculomotor apraxia;   congenital saccade initiation failure
 primary_id: MESH:C537423
 alt_id: MIM:257550
 xref: GARD:16;   ORDO:1404


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15726
    syndrome 10497
      Cogan syndrome 1
        ocular motor apraxia, Cogan type 0
Path 2
Term Annotations click to browse term
  disease 15726
    disease of anatomical entity 15371
      nervous system disease 13482
        central nervous system disease 12044
          brain disease 11319
            disease of mental health 8189
              developmental disorder of mental health 5599
                specific developmental disorder 4566
                  communication disorder 399
                    agnosia 75
                      apraxia 35
                        ocular motor apraxia, Cogan type 0
paths to the root