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Term:Maroteaux Fonfria Syndrome
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Accession:DOID:9001430 term browser browse the term
Synonyms:exact_synonym: Apert syndrome with polydactyly of hands and feet;   Apparent Apert syndrome with polydactyly
 primary_id: MESH:C536023;   RDO:0001434
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Path 1
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  disease 15502
    syndrome 5379
      Maroteaux Fonfria Syndrome 0
Path 2
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  disease 15502
    disease of anatomical entity 14856
      Skin and Connective Tissue Diseases 5066
        connective tissue disease 3771
          bone disease 3277
            bone development disease 1089
              dysostosis 316
                synostosis 209
                  craniosynostosis 172
                    acrocephalosyndactylia 8
                      Maroteaux Fonfria Syndrome 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.