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ONTOLOGY REPORT - ANNOTATIONS


Term:Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual Disability
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Accession:DOID:9005747 term browser browse the term
Synonyms:primary_id: RDO:9000674
For additional species annotation, visit the Alliance of Genome Resources.


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Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual Disability term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Auts2 AUTS2, activator of transcription and developmental regulator JBrowse link 12 27,155,362 28,252,752 RGD:8554872
G Caln1 calneuron 1 JBrowse link 12 29,307,117 29,796,996 RGD:8554872
G Galnt17 polypeptide N-acetylgalactosaminyltransferase 17 JBrowse link 12 28,381,879 29,268,457 RGD:8554872
G Pom121 POM121 transmembrane nucleoporin JBrowse link 12 24,316,575 24,341,943 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
          Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual Disability 4
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
                  intellectual disability 1146
                    Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual Disability 4
paths to the root