Hypertrophic osteoarthropathy, primary, autosomal recessive, 2

MONDO:0013756

Any primary hypertrophic osteoarthropathy in which the cause of the disease is a mutation in the SLCO2A1 gene.

Also known as: SLCO2A1 primary hypertrophic osteoarthropathy, hypertrophic osteoarthropathy, primary, autosomal recessive 2, hypertrophic osteoarthropathy, primary, autosomal recessive, 2, hypertrophic osteoarthropathy, primary, autosomal recessive, type 2, primary hypertrophic osteoarthropathy caused by mutation in SLCO2A1, PDP, autosomal recessive, PHOAR2, pachydermoperiostosis, autosomal recessive

0 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic osteoarthropathy, primary, autosomal recessive, 2 itself.

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Including sub-types (0) Tagged with Hypertrophic osteoarthropathy, primary, autosomal recessive, 2 (0)

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