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ONTOLOGY REPORT - ANNOTATIONS


Term:Kenny Caffey Syndrome
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Accession:DOID:9008715 term browser browse the term
Synonyms:exact_synonym: Dwarfism, cortical thickening of tubular bones, and transient hypocalcemia;   KCS2;   Kenny syndrome;   Kenny-Caffey syndrome, type 2
 primary_id: MESH:C537020;   RDO:0002771
 alt_id: OMIM:127000
For additional species annotation, visit the Alliance of Genome Resources.


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Kenny Caffey Syndrome 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 14759
    syndrome 4210
      Kenny Caffey Syndrome 2
Path 2
Term Annotations click to browse term
  disease 14759
    disease of anatomical entity 13978
      musculoskeletal system disease 3973
        connective tissue disease 2568
          bone disease 2114
            bone development disease 891
              osteochondrodysplasia 402
                Caffey disease 6
                  Kenny Caffey Syndrome 2
paths to the root