Diagnosis Code: 758.89

Short Description: Oth con d/t chrm anm NEC

Long Description: Other conditions due to chromosome anomalies

Code Classification:

• Congenital anomalies (740–759)
  • Congenital anomalies (740-759)
    • 758 Chromosomal anomalies
      • 758.89 Oth con d/t chrm anm NEC

Code Version: 2015 ICD-9-CM

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
• Group chromosomal alteration
• Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
• Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation
• Male with sex chromosome mosaicism
• Methyl-cytosine phosphate guanine binding protein-2 duplication syndrome
• Mitochondrial mutation
• Monosomy 21, mosaicism
• Mosaic variegated aneuploidy syndrome
• Opitz-Frias syndrome
• Pallister-Killian syndrome
• Partial tetrasomy 9 syndrome
• Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
• Ring chromosome 1 syndrome
• Ring chromosome 10 syndrome
• Ring chromosome 11 syndrome
• Ring chromosome 14 syndrome
• Ring chromosome 18 syndrome
• Ring chromosome 20 syndrome
• Ring chromosome 21 syndrome
• Ring chromosome 4 syndrome
• Ring chromosome 9 syndrome
• Schöpf-Schulz-Passarge syndrome
• Snyder-Robinson x-linked mental retardation syndrome
• Spondylocarpotarsal synostosis syndrome
• Spondyloepimetaphyseal dysplasia, Strudwick type
• Spondyloperipheral dysplasia
• Tetrasomy 18p
• 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
• X-linked mental retardation, syndromic 13

References to Index of Diseases and Injuries

The code 758.89 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Abnormal, abnormality, abnormalities - see also Anomaly
  • chromosomal NEC 758.89
    • analysis, nonspecific result 795.2
    • autosomes (see also Abnormal, autosomes NEC) 758.5
    • fetal, (suspected) affecting management of pregnancy 655.1
    • sex 758.81

• Anomaly, anomalous (congenital) (unspecified type) 759.9
  • chromosomes, chromosomal 758.9
    • mosaics 758.89

• Syndrome - see also Disease
  • due to abnormality
    • chromosomal 758.89
      • sex 758.81

• Translocation
  • chromosomes NEC 758.89

Crosswalk Information

The code 758.89 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

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