disease has feature Increased bone mineral density syndromic disease hereditary disease primary hypertrophic osteoarthropathy https://github.com/monarch-initiative/mondo/issues/3395 https://www.malacards.org/card/primary_hypertrophic_osteoarthropathy hypertrophic osteoarthropathy, primary, autosomal recessive, 1 A genetically and clinically heterogeneous inherited disorder characterized by digital clubbing and osteoarthropathy, with variable features of pachydermia, delayed closure of the fontanels, and congenital heart disease. There are two types of PHO: pachydermoperiostosis and cranio-osteoarthropathy. NANDO:1200642 NANDO:2201004 Orphanet:248095 PHO NANDO:2100288 hypertrophic osteoarthropathy, primary SCTID:88220006 hypertropic osteoarthropathy, primary PDP DOID:14283 OMIMPS:259100 PHOAR1 pachydermoperiostosis of nail [ambiguous] idiopathic hypertrophic osteoarthropathy MESH:D010004 Touraine-Solente-Gole syndrome MONDO:0016620 Orphanet:2796 pachydermoperiostosis UMLS:C0029411 MedDRA:10051686 MEDGEN:18210 icd11.foundation:792225761 NCIT:C85023 GARD:0020667 hypertrophic osteoarthropathy, primary, autosomal recessive, type 1 Touraine Solente Gole syndrome obsolete primary bone dysplasia with increased bone density dermis disorder