Free ICD-9-CM Diagnosis Codes
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2008
> Congential Anomalies
740-759
> Chromosomal anomalies
758.*
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2008 ICD-9-CM Diagnosis Code 758.9
Conditions due to anomaly of unspecified chromosome
758.89
759
758.9 is a billable ICD-9-CM medical code that can be used to specify a diagnosis on a reimbursement claim.
Newer versions of 758.9:
2009
2010
Diagnosis Definition(s)
clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material, either a whole chromosome or a chromosome segment.
ICD-9-CM Volume 2 Index Entries That Refer To 758.9
Anomaly, anomalous (congenital) (unspecified type)
759.9
chromosomes, chromosomal
758.9
13 (13-15)
758.1
18 (16-18)
758.2
21 or 22
758.0
autosomes NEC (see also Abnormal, autosomes)
758.5
deletion
758.39
Christchurch
758.39
D1
758.1
758.2
G
758.0
mitochondrial
758.9
mosaics
758.89
sex
758.81
complement, XO
758.6
complement, XXX
758.81
complement, XXY
758.7
complement, XYY
758.81
gonadal dysgenesis
758.6
Klinefelter's
758.7
Turner's
758.6
trisomy 21
758.0
Mosaicism, mosaic (chromosomal)
758.9
autosomal
758.5
sex
758.81