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GTR Home > Conditions/Phenotypes > Brachydactyly type A2


Brachydactyly type A2 is an autosomal dominant disorder characterized by malformations of the middle phalanx of the index finger and by anomalies of the second toe (summary by Su et al., 2011). [from OMIM]

Available tests

42 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: BDA2, BMP2A, SSFSC, SSFSC1, BMP2
    Summary: bone morphogenetic protein 2

  • Also known as: ALK-6, ALK6, AMD3, AMDD, BDA1D, BDA2, CDw293, BMPR1B
    Summary: bone morphogenetic protein receptor type 1B

  • Also known as: BDA1C, BMP-14, BMP14, CDMP1, DUPANS, LAP-4, LAP4, OS5, SYM1B, SYNS2, GDF5
    Summary: growth differentiation factor 5

Clinical features


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