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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:exotropia
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Accession:DOID:1143 term browser browse the term
Definition:A form of ocular misalignment where the visual axes diverge inappropriately. For example, medial rectus muscle weakness may produce this condition as the affected eye will deviate laterally upon attempted forward gaze. An exotropia occurs due to the relatively unopposed force exerted on the eye by the lateral rectus muscle, which pulls the eye in an outward direction.
Synonyms:exact_synonym: divergent concomitant strabismus;   divergent strabismus;   exodeviation;   exodeviations;   exophoria;   primary exotropia;   secondary exotropia
 narrow_synonym: CONCOMITANT EXOTROPIA
 primary_id: MESH:D005099
 xref: ICD10CM:H50.1;   ICD9CM:378.1;   NCI:C34601
For additional species annotation, visit the Alliance of Genome Resources.

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show annotations for term's descendants           Sort by:
exotropia term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Auts2 activator of transcription and developmental regulator AUTS2 ISO ClinVar Annotator: match by term: concomitant exotropia ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004936543:5,146,961...6,187,634 JBrowse link
G Cdh3 cadherin 3 ISO ClinVar Annotator: match by term: concomitant exotropia ClinVar PMID:28492532 NCBI chrNW_004936475:18,908,031...18,954,402
Ensembl chrNW_004936475:18,906,493...18,955,072 		JBrowse link
G Col4a2 collagen type IV alpha 2 chain ISO ClinVar Annotator: match by term: concomitant exotropia ClinVar PMID:28492532 NCBI chrNW_004936472:2,270,836...2,416,324
Ensembl chrNW_004936472:2,270,819...2,416,349 		JBrowse link
G Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 ISO ClinVar Annotator: match by term: concomitant exotropia ClinVar NCBI chrNW_004936471:38,419,147...38,606,312
Ensembl chrNW_004936471:38,419,129...38,606,323 		JBrowse link
G LOC101976443 lipoxygenase homology PLAT domains 1 ISO ClinVar Annotator: match by term: concomitant exotropia ClinVar PMID:24033266 PMID:26467025 PMID:28492532 PMID:29799290 PMID:30311386 NCBI chrNW_004936517:271,909...409,818
Ensembl chrNW_004936517:271,909...409,691 		JBrowse link
G Pomgnt2 protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) ISO ClinVar Annotator: match by term: concomitant exotropia ClinVar PMID:25741868 PMID:28492532 NCBI chrNW_004936695:2,117,506...2,141,859
Ensembl chrNW_004936695:2,139,661...2,141,403 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14633
    sensory system disease 6687
      eye disease 3443
        ocular motility disease 239
          strabismus 44
            exotropia 6
              alternating exotropia 0
              monocular exotropia 0
Path 2
Term Annotations click to browse term
  disease 14633
    disease of anatomical entity 14323
      nervous system disease 12606
        Neurologic Manifestations 9413
          sensory system disease 6687
            eye disease 3443
              refractive error 235
                hyperopia 51
                  strabismus 44
                    exotropia 6
                      alternating exotropia 0
                      monocular exotropia 0
paths to the root