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2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Congenital Anomalies 740-759 > Chromosomal Anomalies 758.* > 2007 ICD-9-CM Diagnosis 758.1 Patau's syndrome This code may be outdated. View the most recent version of ICD-9-CM 758.1 The presence of an additional (third) chromosome on an otherwise diploid chromosome 13 with variable abnormalities, most characteristic of which are microcephaly, microphthalmia, hypertelorism, cleft lip or palate, polydactyly, and cardiovascular, genitourinary, and neurological abnormalities. It is one of the most frequent causes of perinatal deaths. 758.1 is a specific code that can be used to specify a diagnosis 758.1 contains 19 index entries View the ICD-9-CM Volume 1 758.* hierarchy 758.1 also known as: Trisomy: 13 D1 Index entries containing 758.1: Abnormal, abnormality, abnormalities - see also Anomaly autosomes NEC 758.5 13 758.1 D1 758.1 Accessory (congenital) chromosome(s) NEC 758.5 13-15 758.1 D1 758.1 Additional - see also Accessory chromosome(s) 758.5 13-15 758.1 Anomaly, anomalous (congenital) (unspecified type) 759.9 chromosomes, chromosomal 758.9 13 (13-15) 758.1 D1 758.1 Arrhinencephaly 742.2 due to trisomy 13 (13-15) 758.1 Holoprosencephaly 742.2 due to trisomy 13 758.1 Patau's syndrome (trisomy D1) 758.1 Syndrome - see also Disease due to abnormality autosomal NEC (see also Abnormal, autosomes NEC) 758.5 13 758.1 D1 758.1 Patau's (trisomy D1) 758.1 trisomy NEC 758.5 13 or D1 758.1 Translocation autosomes NEC 758.5 13-15 758.1 D1 758.1 Trisomy (syndrome) NEC 758.5 13 (partial) 758.1 D1 758.1 group D1 758.1