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ONTOLOGY REPORT - ANNOTATIONS


Term:Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism
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Accession:DOID:9006612 term browser browse the term
Synonyms:exact_synonym: PMRED
 primary_id: OMIM:614501;   RDO:9000660
For additional species annotation, visit the Alliance of Genome Resources.


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Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Snip1 Smad nuclear interacting protein 1 JBrowse link 15 19,275,273 19,282,753 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15620
    disease of anatomical entity 14949
      musculoskeletal system disease 4277
        Musculoskeletal Abnormalities 1302
          Craniofacial Abnormalities 1046
            Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism 1
Path 2
Term Annotations click to browse term
  disease 15620
    disease of anatomical entity 14949
      nervous system disease 10219
        central nervous system disease 8096
          brain disease 7565
            epilepsy 1080
              Psychomotor Retardation, Epilepsy, and Craniofacial Dysmorphism 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.