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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;   RDO:9001754
For additional species annotation, visit the Alliance of Genome Resources.


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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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14025
    syndrome 4467
      RAHMAN SYNDROME 1
Path 2
Term Annotations click to browse term
  disease 14025
    disease of anatomical entity 13238
      nervous system disease 8245
        central nervous system disease 5483
          brain disease 5121
            thalamic disease 195
              hypothalamic disease 195
                pituitary gland disease 154
                  hyperpituitarism 35
                    Gigantism 12
                      RAHMAN SYNDROME 1
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