Hypertrophic osteoarthropathy, primary, autosomal recessive, 1

MONDO:0024546

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

Also known as: HPGD primary hypertrophic osteoarthropathy, hypertrophic osteoarthropathy, primary, autosomal recessive 1, hypertrophic osteoarthropathy, primary, autosomal recessive, 1, primary hypertrophic osteoarthropathy caused by mutation in HPGD, Cranioosteoarthropathy, Currarino idiopathic osteoarthropathy, PDP, autosomal recessive, PHOAR1

0 clinical trials for this condition and its sub-types, 0 tagged with Hypertrophic osteoarthropathy, primary, autosomal recessive, 1 itself.

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Including sub-types (0) Tagged with Hypertrophic osteoarthropathy, primary, autosomal recessive, 1 (0)

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