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ONTOLOGY REPORT - ANNOTATIONS


Term:CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES
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Accession:DOID:9003251 term browser browse the term
Synonyms:exact_synonym: CADEDS
 primary_id: OMIM:617643;   RDO:9005145
For additional species annotation, visit the Alliance of Genome Resources.


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CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G KCNMA1 potassium calcium-activated channel subfamily M alpha 1 JBrowse link 10 76,869,601 77,637,969 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16489
    Developmental Diseases 10312
      Neurodevelopmental Disorders 5303
        Developmental Disabilities 486
          CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES 1
Path 2
Term Annotations click to browse term
  disease 16489
    disease of anatomical entity 15414
      nervous system disease 11652
        sensory system disease 4824
          eye and adnexa disease 2309
            eye disease 2309
              visual pathway disease 536
                visual cortex disease 534
                  visual epilepsy 534
                    CEREBELLAR ATROPHY, DEVELOPMENTAL DELAY, AND SEIZURES 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.