Morgagni-Stewart-Morel syndrome https://rarediseases.info.nih.gov/diseases/8593/morgagni-stewart-morel-syndrome https://www.malacards.org/card/hyperostosis_frontalis_interna MSM syndrome NCIT:C84772 Morgagni-Stewart-Morel syndrome is characterized by thickening of the inner table of the frontal bone, sometimes associated with obesity and hypertrichosis. It mainly affects women over 35 years of age. The prevalence and clinical significance of hyperostosis frontalis interna is unknown. Transmission is either X-linked or autosomal dominant. OMIM:144800 GARD:0008593 Hyperostosis Frontalis Interna Orphanet:77296 hyperostosis frontalis interna SCTID:82054006 MESH:D006957 NORD:1268 MONDO:0007766 MEDGEN:9367 UMLS:C0020494 Morgagni-Stewart-Morel syndrome hyperostosis frontalis interna, obesity, shortness and cognitive impairment disorder of development or morphogenesis