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ONTOLOGY REPORT - ANNOTATIONS


Term:Rahman Syndrome
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Accession:DOID:9002839 term browser browse the term
Definition:A disease characterized by mild to severe intellectual disability associated with variable somatic overgrowth manifest as increased birth length, height, weight, and/or head circumference. (OMIM)
Synonyms:exact_synonym: RMNS
 primary_id: OMIM:617537
 alt_id: RDO:9001754
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Rahman Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G H1f4 H1.4 linker histone, cluster member JBrowse link 17 43,734,461 43,735,120 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16022
    syndrome 6143
      Rahman Syndrome 1
Path 2
Term Annotations click to browse term
  disease 16022
    disease of anatomical entity 15275
      nervous system disease 10770
        central nervous system disease 8860
          brain disease 8147
            thalamic disease 189
              hypothalamic disease 189
                pituitary gland disease 146
                  hyperpituitarism 34
                    Gigantism 9
                      Rahman 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.