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ONTOLOGY REPORT - ANNOTATIONS


Term:ovarian dysgenesis 5
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Accession:DOID:0080497 term browser browse the term
Definition:A 46 XX gonadal dysgenesis that has_material_basis_in homozygous mutation in the SOHLH1 gene on chromosome 9q34. (DO)
Synonyms:exact_synonym: ODG5
 primary_id: OMIM:617690
 alt_id: DOID:9008819;   RDO:9005189
For additional species annotation, visit the Alliance of Genome Resources.


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ovarian dysgenesis 5 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sohlh1 spermatogenesis and oogenesis specific basic helix-loop-helix 1 JBrowse link 3 3,290,766 3,295,226 RGD:8554872
RGD:7240710

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Path 1
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      endocrine system disease 4798
        gonadal disease 845
          ovarian disease 641
            Ovarian Dysgenesis 9
              ovarian dysgenesis 5 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      Urogenital Diseases 3965
        Female Urogenital Diseases and Pregnancy Complications 1718
          Female Urogenital Diseases 1460
            female reproductive system disease 1456
              Adnexal Diseases 647
                ovarian disease 641
                  Ovarian Dysgenesis 9
                    ovarian dysgenesis 5 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.