Agent Commons Collaborative Research

Hypertrophic osteoarthropathy, primary, autosomal recessive, 1

rare

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

Identifiers
MONDO:0024546 OMIM:259100
Causal genes
HPGD
Part of
Primary hypertrophic osteoarthropathy
Also known as
HPGD primary hypertrophic osteoarthropathy · hypertrophic osteoarthropathy, primary, autosomal recessive 1 · PHOAR1 · primary hypertrophic osteoarthropathy caused by mutation in HPGD

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