Chromosome ICD-10 Code

  • Q98.9 - Sex chromosome abnormality, male phenotype, unspecified
  • Q98.6 - Male with structurally abnormal sex chromosome
  • Q99.8 - Other specified chromosome abnormalities
  • Q95.1 - Chromosome inversion in normal individual
  • Q99.0 - Chimera 46, XX/46, XY
  • Q99.8 - Other specified chromosome abnormalities
  • Q99.1 - 46, XX true hermaphrodite
  • Q99.9 - Chromosomal abnormality, unspecified
  • Q99.2 - Fragile X chromosome
  • Q99.1 - 46, XX true hermaphrodite
  • Q93.3 - Deletion of short arm of chromosome 4
  • Q93.4 - Deletion of short arm of chromosome 5
  • Q93.5 - Other deletions of part of a chromosome
  • Q93.59 - Other deletions of part of a chromosome
  • Q93.1 - Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
  • Q93.0 - Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
  • Q93.2 - Chromosome replaced with ring, dicentric or isochromosome
  • Q97.2 - Mosaicism, lines with various numbers of X chromosomes
  • Q98.8 - Other specified sex chromosome abnormalities, male phenotype
  • Q98.9 - Sex chromosome abnormality, male phenotype, unspecified
  • Q98.7 - Male with sex chromosome mosaicism
  • Q97.8 - Other specified sex chromosome abnormalities, female phenotype
  • Q97.9 - Sex chromosome abnormality, female phenotype, unspecified
  • Q97.0 - Karyotype 47, XXX
  • Q97.3 - Female with 46, XY karyotype
  • Q97.1 - Female with more than three X chromosomes
  • Q98.5 - Karyotype 47, XYY
  • Q98.3 - Other male with 46, XX karyotype
  • O35.15 - Maternal care for (suspected) chromosomal abnormality in fetus, sex chromosome abnormality
  • Q98.6 - Male with structurally abnormal sex chromosome
  • Q96.2 - Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
  • Q93.51 - Angelman syndrome
  • Q93.52 - Phelan-McDermid syndrome
  • Q98.1 - Klinefelter syndrome, male with more than two X chromosomes
  • Q98.4 - Klinefelter syndrome, unspecified
  • Q98.0 - Klinefelter syndrome karyotype 47, XXY
  • Q96.4 - Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
  • Q92.0 - Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
  • Q92.1 - Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
  • Q98.1 - Klinefelter syndrome, male with more than two X chromosomes