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ONTOLOGY REPORT - ANNOTATIONS


Term:hypogonadotropic hypogonadism 6 with or without anosmia
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Accession:DOID:0090086 term browser browse the term
Definition:A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the FGF8 gene on chromosome 10q24, sometimes in association with mutation in another gene. (DO)
Synonyms:primary_id: RDO:9003764
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hypogonadotropic hypogonadism 6 with or without anosmia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fgf8 fibroblast growth factor 8 JBrowse link 1 265,492,949 265,498,965 RGD:13592920

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          hypogonadotropic hypogonadism 6 with or without anosmia 1
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      endocrine system disease 4706
        gonadal disease 838
          hypogonadism 108
            hypogonadotropic hypogonadism 35
              hypogonadotropic hypogonadism 6 with or without anosmia 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.