ONTOLOGY REPORT - ANNOTATIONS


Term:Gigantism
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Accession:DOID:9006084 term browser browse the term
Definition:The condition of accelerated and excessive GROWTH in children or adolescents who are exposed to excess HUMAN GROWTH HORMONE before the closure of EPIPHYSES. It is usually caused by somatotroph hyperplasia or a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. These patients are of abnormally tall stature, more than 3 standard deviations above normal mean height for age.
Synonyms:exact_synonym: Pituitary Gigantism
 primary_id: MESH:D005877;   RDO:0003166
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Gigantism term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ankrd26 ankyrin repeat domain 26 JBrowse link 4 150,548,656 150,616,928 RGD:9681744
G Nsd1 nuclear receptor binding SET domain protein 1 JBrowse link 17 9,840,859 9,955,391 RGD:11568154
RAHMAN SYNDROME term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hist1h1e histone cluster 1 H1 family member e JBrowse link 17 43,734,461 43,735,120 RGD:8554872
RGD:7240710
Simpson-Golabi-Behmel syndrome type 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gpc3 glypican 3 JBrowse link X 139,579,268 139,947,093 RGD:7240710
RGD:8554872
G Gpc4 glypican 4 JBrowse link X 139,354,325 139,464,876 RGD:11554173
G Med12 mediator complex subunit 12 JBrowse link X 71,174,653 71,197,812 RGD:8554872
G Retsat retinol saturase JBrowse link 4 100,465,365 100,474,128 RGD:11554173
TATTON-BROWN-RAHMAN SYNDROME term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dnmt3a DNA methyltransferase 3 alpha JBrowse link 6 28,205,375 28,346,052 RGD:7240710
RGD:8554872
Tenorio Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rnf125 ring finger protein 125 JBrowse link 18 15,193,226 15,225,454 RGD:7240710
RGD:8554872
THAUVIN-ROBINET-FAIVRE SYNDROME term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fibp FGF1 intracellular binding protein JBrowse link 1 220,840,078 220,844,412 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14919
    Developmental Diseases 7761
      bone development disease 894
        Gigantism 12
          RAHMAN SYNDROME 1
          Simpson-Golabi-Behmel syndrome type 1 4
          TATTON-BROWN-RAHMAN SYNDROME 1
          THAUVIN-ROBINET-FAIVRE SYNDROME 1
          Tenorio Syndrome 1
Path 2
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      nervous system disease 9147
        central nervous system disease 6945
          brain disease 6451
            thalamic disease 197
              hypothalamic disease 197
                pituitary gland disease 158
                  hyperpituitarism 35
                    Gigantism 12
                      RAHMAN SYNDROME 1
                      Simpson-Golabi-Behmel syndrome type 1 4
                      TATTON-BROWN-RAHMAN SYNDROME 1
                      THAUVIN-ROBINET-FAIVRE SYNDROME 1
                      Tenorio Syndrome 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.