has characteristic has characteristic disease has feature Reduced bone mineral density hereditary disease congenital osteogenesis imperfecta-microcephaly-cataracts syndrome https://github.com/monarch-initiative/mondo/issues/4069 https://www.malacards.org/card/congenital_osteogenesis_imperfecta_microcephaly_cataracts_syndrome https://www.malacards.org/card/osteogenesis_imperfecta_congenita_microcephaly_and_cataracts_2 Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome is characterized by multiple fractures in the prenatal period, microcephaly and bilateral cataracts. It has been described in three infants all of whom died in utero or a few hours after birth. The mode of inheritance appears to be autosomal recessive. MONDO:0009803 MEDGEN:337988 Orphanet:2772 MESH:C537558 UMLS:C1850184 OMIM:259410 GARD:0004139 obsolete primary bone dysplasia with decreased bone density congenital