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
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Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual Disability term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Auts2 activator of transcription and developmental regulator AUTS2 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 14823
    Developmental Diseases 7637
      Neurodevelopmental Disorders 2755
        intellectual disability 1157
          Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual Disability 4
Path 2
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        central nervous system disease 6908
          brain disease 6412
            disease of mental health 4323
              developmental disorder of mental health 2594
                specific developmental disorder 1329
                  intellectual disability 1157
                    Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual Disability 4
paths to the root

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