disease has feature Increased bone mineral density hyperostosis hereditary disease sclerosteosis https://www.malacards.org/card/sclerosteosis SCTID:17568006 ICD9:756.59 DOID:0060251 OMIMPS:269500 cortical hyperostosis-syndactyly syndrome GARD:0004771 MONDO:0017838 NANDO:2201369 UMLS:C0265301 Orphanet:3152 Sclerosteosis is a very rare serious sclerosing hyperostosis syndrome characterized clinically by variable syndactyly and progressive skeletal overgrowth (particularly of the skull), resulting in distinctive facial features (mandibular overgrowth, frontal bossing, midfacial hypoplasia), cranial nerve entrapment causing facial palsy and deafness, and potentially lethal elevation of intracranial pressure. MESH:C537525 cortical hyperostosis with syndactyly icd11.foundation:371637416 NCIT:C131133 MEDGEN:120530 obsolete primary bone dysplasia with increased bone density