2012 ICD-9-CM Diagnosis Code 758.89
Other conditions due to chromosome anomalies
- Short description: Oth con d/t chrm anm NEC.
- ICD-9-CM 758.89 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 758.89 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
- You are viewing the 2012 version of ICD-9-CM 758.89.
- More recent version(s) of ICD-9-CM 758.89: 2013 2014 2015.
Convert to ICD-10-CM:
758.89 converts approximately to:
- 2015/16 ICD-10-CM Q99.8 Other specified chromosome abnormalities
Approximate Synonyms
- 14q partial distal trisomy syndrome
- 14q partial proximal trisomy syndrome
- 14q partial trisomy syndrome
- 16p partial trisomy syndrome
- 16q partial monosomy syndrome
- 2p partial trisomy syndrome
- Anomaly of chromosome pair 1
- Anomaly of chromosome pair 10
- Anomaly of chromosome pair 11
- Anomaly of chromosome pair 12
- Anomaly of chromosome pair 14
- Anomaly of chromosome pair 15
- Anomaly of chromosome pair 16
- Anomaly of chromosome pair 17
- Anomaly of chromosome pair 19
- Anomaly of chromosome pair 2
- Anomaly of chromosome pair 20
- Anomaly of chromosome pair 21
- Anomaly of chromosome pair 3
- Anomaly of chromosome pair 4
- Anomaly of chromosome pair 5
- Anomaly of chromosome pair 6
- Anomaly of chromosome pair 7
- Anomaly of chromosome pair 8
- Anomaly of chromosome pair 9
- Balanced autosomal rearrangement in abnormal individual
- Balanced autosomal translocation
- Balanced rearrangement and structural marker
- Balanced sex/autosomal rearrangement in abnormal individual
- Balanced translocation and insertion in normal individual
- Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency
- Chromosomal alterations of group A
- Chromosomal alterations of group B
- Chromosomal alterations of group C and X
- Chromosomal alterations of group D
- Chromosomal alterations of group E
- Chromosomal alterations of group F
- Chromosomal alterations of group G and Y
- Chromosomal disorder
- Complete trisomy 14 syndrome
- Complete trisomy 16 syndrome
- Duplication of chromosome
- Duplication with other complex rearrangement
- Extra unidentified structurally abnormal chromosome
- Familial extra unidentified structurally abnormal chromosome
- Faun tail syndrome
- Group chromosomal alteration
- Male with sex chromosome mosaicism
- Mitochondrial mutation
- Monosomy 21, mosaicism
- Opitz-Frias syndrome
- Pallister-Killian syndrome
- Partial tetrasomy 9 syndrome
- Ring chromosome 1 syndrome
- Ring chromosome 10 syndrome
- Ring chromosome 11 syndrome
- Ring chromosome 18 syndrome
- Ring chromosome 20 syndrome
- Ring chromosome 21 syndrome
- Ring chromosome 4 syndrome
- Ring chromosome 9 syndrome
- Triploidy syndrome
- Triploidy, diploidy, mixoploidy syndrome
- Unbalanced translocation of chromosome
- Whole chromosome monosomy - meiotic nondisjunction
- Whole chromosome trisomy syndrome
- Whole chromosome trisomy, meiotic nondisjunction
- Whole chromosome trisomy, mosaicism