About: Fibular aplasia-ectrodactyly syndrome

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Fibular aplasia-ectrodactyly syndrome is a very rare genetic disorder which is characterized by aplasia/hypoplasia of the fibula, ectrodactyly, and/or brachydactyly/syndactyly. Additional symptoms include shortness of the femur and tibial/knee/hip/ankle defects. This disorder is inherited in an autosomal dominant manner.

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  • Fibular aplasia-ectrodactyly syndrome is a very rare genetic disorder which is characterized by aplasia/hypoplasia of the fibula, ectrodactyly, and/or brachydactyly/syndactyly. Additional symptoms include shortness of the femur and tibial/knee/hip/ankle defects. This disorder is inherited in an autosomal dominant manner. (en)
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  • (en)
  • Brachydactyly-ectrodactyly with fibular aplasia or hypoplasia (en)
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  • 70777463 (xsd:integer)
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  • Fibular aplasia-ectrodactyly syndrome (en)
dbp:synonyms
  • Brachydactyly-ectrodactyly with fibular aplasia or hypoplasia (en)
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  • Fibular aplasia-ectrodactyly syndrome is a very rare genetic disorder which is characterized by aplasia/hypoplasia of the fibula, ectrodactyly, and/or brachydactyly/syndactyly. Additional symptoms include shortness of the femur and tibial/knee/hip/ankle defects. This disorder is inherited in an autosomal dominant manner. (en)
rdfs:label
  • Fibular aplasia-ectrodactyly syndrome (en)
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