| Disease Aliases (20) | Cio Coa Cranioosteoarthropathy Currarino idiopathic osteoarthropathy Familial idiopathic osteoarthropathy of childhood Hpgd primary hypertrophic osteoarthropathy Idiopathic hypertrophic osteoarthropathy Pachydermoperiostosis, autosomal recessive Pdp Pdp, autosomal recessive Pho, autosomal recessive Phoar1 Pachydermoperiostosis Primary hypertrophic osteoarthropathy Touraine-solente-gole syndrome Touraine solente gole syndrome Hypertrophic osteoarthropathy, primary, autosomal recessive, 1 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 Hypertrophic osteoarthropathy, primary, autosomal recessive, type 1 Primary hypertrophic osteoarthropathy caused by mutation in hpgd |
Associated Genes (2) NCBI-RefSeq: SLCO2A1 (Solute carrier organic anion transporter family member 2A1) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: HPGD (15-hydroxyprostaglandin dehydrogenase) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Hypertrophic osteoarthropathy | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |