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- Bbaeef9a8401718342683aabff9519a2c hasDbXref "Orphanet:2772" @default.
- Bbaeef9a8401718342683aabff9519a2c type Axiom @default.
- Bbaeef9a8401718342683aabff9519a2c annotatedProperty IAO_0000115 @default.
- Bbaeef9a8401718342683aabff9519a2c annotatedSource MONDO_0009803 @default.
- Bbaeef9a8401718342683aabff9519a2c annotatedTarget "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." @default.