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ONTOLOGY REPORT - ANNOTATIONS


Term:Congenital Nongoitrous Hypothyroidism 8
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Accession:DOID:9001092 term browser browse the term
Synonyms:exact_synonym: CHNG8
 primary_id: OMIM:301033
For additional species annotation, visit the Alliance of Genome Resources.


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Congenital Nongoitrous Hypothyroidism 8 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tbl1x transducin (beta)-like 1 X-linked JBrowse link X 44,959,883 44,988,551 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15603
    syndrome 5215
      hypothyroidism 140
        congenital hypothyroidism 46
          Congenital Nongoitrous Hypothyroidism 10
            Congenital Nongoitrous Hypothyroidism 8 1
Path 2
Term Annotations click to browse term
  disease 15603
    disease of anatomical entity 14934
      musculoskeletal system disease 4302
        connective tissue disease 2790
          bone disease 2242
            bone development disease 1001
              Dwarfism 309
                congenital hypothyroidism 46
                  Congenital Nongoitrous Hypothyroidism 10
                    Congenital Nongoitrous Hypothyroidism 8 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.