ONTOLOGY REPORT - ANNOTATIONS


Term:cerebral cavernous malformation 3
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Accession:DOID:0060671 term browser browse the term
Definition:A cerebral cavernous malformation that_has_material_basis in mutation in the PDCD10 gene on chromosome 3q26.1. (DO)
Synonyms:exact_synonym: CCM3;   CEREBRAL CAVERNOUS MALFORMATIONS 3
 primary_id: MESH:C566393;   RDO:0014760
 alt_id: OMIM:603285
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cerebral cavernous malformation 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Pdcd10 programmed cell death 10 JBrowse link 2 173,966,701 174,012,730 RGD:7240710
RGD:8554872

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  disease 14920
    Developmental Diseases 7769
      Neurodevelopmental Disorders 2765
        intellectual disability 1594
          cerebral cavernous malformation 3 1
Path 2
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  disease 14920
    disease of anatomical entity 14086
      Hemic and Lymphatic Diseases 1591
        hematopoietic system disease 1375
          blood coagulation disease 392
            hemorrhagic disease 378
              vascular hemostatic disease 184
                cavernous hemangioma 10
                  cerebral cavernous malformation 10
                    cerebral cavernous malformation 3 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.