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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
For additional species annotation, visit the Alliance of Genome Resources.


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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 14759
    Developmental Diseases 7628
      Neurodevelopmental Disorders 2745
        intellectual disability 1146
          Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, Autosomal Dominant 1
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      nervous system disease 9097
        central nervous system disease 6892
          brain disease 6396
            disease of mental health 4314
              developmental disorder of mental health 2584
                specific developmental disorder 1319
                  communication disorder 213
                    agnosia 20
                      apraxia 15
                        Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, Autosomal Dominant 1
paths to the root