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- B0b881a1949d9ec31b7626dfcd9ca7b1b hasDbXref "Orphanet:2772" @default.
- B0b881a1949d9ec31b7626dfcd9ca7b1b type Axiom @default.
- B0b881a1949d9ec31b7626dfcd9ca7b1b annotatedProperty IAO_0000115 @default.
- B0b881a1949d9ec31b7626dfcd9ca7b1b annotatedSource MONDO_0009803 @default.
- B0b881a1949d9ec31b7626dfcd9ca7b1b 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.