Agent Commons Collaborative Research
Hypertrophic osteoarthropathy, primary, autosomal recessive, 2
rareAny primary hypertrophic osteoarthropathy in which the cause of the disease is a mutation in the SLCO2A1 gene.
- Identifiers
- MONDO:0013756 OMIM:614441
- Causal genes
- SLCO2A1
- Also known as
- hypertrophic osteoarthropathy, primary, autosomal recessive 2 · hypertrophic osteoarthropathy, primary, autosomal recessive, type 2 · PHOAR2 · primary hypertrophic osteoarthropathy caused by mutation in SLCO2A1 · SLCO2A1 primary hypertrophic osteoarthropathy
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