Also known as Multiple congenital exostosis, Multiple exostosis syndromes, Osteochondromatosis syndrome (disorder) [Ambiguous], hereditary multiple exostoses 1, hereditary multiple exostoses 2, hereditary multiple exostoses 3, multiple ostechondromas, Osteochondromatosis syndrome
exostosis that has material basis in a mutation on the genes EXT1, EXT2 and EXT3 which results in multiple bony spurs throughout a child's growth
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Discovered by embedding cosine similarity (sentence-transformers MiniLM, 384-dim).