craniosynostosis-fibular aplasia syndrome https://github.com/monarch-initiative/mondo/issues/6751 https://www.malacards.org/card/craniosynostosis_with_fibular_aplasia OMIM:218550 UMLS:C1857492 GARD:0024646 craniosynostosis with fibular aplasia Craniosynostosis-fibular aplasia is an extremely rare genetic disease, reported in only 2 brothers to date, characterized by the combination of craniosynostosis (involving both coronal sutures), congenital absence of the fibula, cryptorchidism, and bilateral simian creases. Intelligence is normal and an autosomal recessive mode of inheritance has been proposed. There have been no further reports in the literature since 1972. MONDO:0009038 Lowry syndrome SCTID:732250002 MESH:C565665 Orphanet:1533 MEDGEN:347468 syndromic craniosynostosis