ONTOLOGY REPORT - ANNOTATIONS


Term:Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, Autosomal Dominant
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Accession:DOID:9007175 term browser browse the term
Synonyms:exact_synonym: ADRESD;   RESDAD
 primary_id: MESH:C563392;   RDO:0012659
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Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, Autosomal Dominant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Grin2a glutamate ionotropic receptor NMDA type subunit 2A JBrowse link 10 5,707,806 6,123,568 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14926
    Developmental Diseases 7782
      Neurodevelopmental Disorders 2775
        intellectual disability 1599
          Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, Autosomal Dominant 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14096
      nervous system disease 9148
        central nervous system disease 6948
          brain disease 6452
            disease of mental health 4334
              developmental disorder of mental health 2608
                specific developmental disorder 1771
                  communication disorder 217
                    agnosia 20
                      apraxia 15
                        Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, Autosomal Dominant 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.