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ONTOLOGY REPORT - ANNOTATIONS


Term:Kenny-Caffey Syndrome, Type 2
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Accession:DOID:9008715 term browser browse the term
Synonyms:exact_synonym: KCS2;   Kenny syndrome;   Kenny-Caffey syndrome 2;   dwarfism, cortical thickening of tubular bones, and transient hypocalcemia
 primary_id: MESH:C537020
 alt_id: OMIM:127000;   RDO:0002771
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Kenny-Caffey Syndrome, Type 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fam111a family with sequence similarity 111, member A JBrowse link 1 229,003,778 229,019,532 RGD:7240710
RGD:8554872
G Tbce tubulin folding cofactor E JBrowse link 17 53,983,126 54,029,028 RGD:11554173

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15590
    syndrome 5131
      Kenny-Caffey Syndrome 2
        Kenny-Caffey Syndrome, Type 2 2
Path 2
Term Annotations click to browse term
  disease 15590
    disease of anatomical entity 14919
      Skin and Connective Tissue Diseases 4196
        connective tissue disease 2761
          bone disease 2210
            bone development disease 980
              osteochondrodysplasia 406
                Caffey disease 5
                  Kenny-Caffey Syndrome 2
                    Kenny-Caffey Syndrome, Type 2 2
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.