758.89 - Other Conditions Due To Chromosome Anomalies
The ICD 9 Code for Other conditions due to chromosome anomalies is listed as 758.89.
Additional information concerning this code and description can be found below including ICD 10 crosswalks / GEMS, and chapter information where available.
| ICD 9 CM Field | Value |
|---|---|
| Diagnosis Code: | 758.89 |
| Long Description: | Other conditions due to chromosome anomalies |
| Short Description: | Oth con d/t chrm anm NEC |
| Chapter: | Congenital Anomalies |
| Block: | Chromosomal anomalies (758-758) |
| Related Descriptions: |
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 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 |
| ICD-10-CM Diagnosis Codes General Equivalence Mappings (GEMS): | |
| ICD-10-CM Code: | Q99.8 - Other specified chromosome abnormalities (approximate) |
| ICD-9-CM Siblings (same level / similar specificity) of 758.89: | |
| 758.81 - Other conditions due to sex chromosome anomalies | |