Billable/Specific ICD-10-CM Codes - Page 209

There are 35,750 ICD-10-CM codes which are billable/specific and can be used to indicate a diagnosis for reimbursement purposes as there are no codes with a greater level of specificity under each code.

  • Q89.2 - Congenital malformations of other endocrine glands
  • Q89.3 - Situs inversus
  • Q89.4 - Conjoined twins
  • Q89.7 - Multiple congenital malformations, not elsewhere classified
  • Q89.8 - Other specified congenital malformations
  • Q89.9 - Congenital malformation, unspecified
  • Q90.0 - Trisomy 21, nonmosaicism (meiotic nondisjunction)
  • Q90.1 - Trisomy 21, mosaicism (mitotic nondisjunction)
  • Q90.2 - Trisomy 21, translocation
  • Q90.9 - Down syndrome, unspecified
  • Q91.0 - Trisomy 18, nonmosaicism (meiotic nondisjunction)
  • Q91.1 - Trisomy 18, mosaicism (mitotic nondisjunction)
  • Q91.2 - Trisomy 18, translocation
  • Q91.3 - Trisomy 18, unspecified
  • Q91.4 - Trisomy 13, nonmosaicism (meiotic nondisjunction)
  • Q91.5 - Trisomy 13, mosaicism (mitotic nondisjunction)
  • Q91.6 - Trisomy 13, translocation
  • Q91.7 - Trisomy 13, unspecified
  • Q92.0 - Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction)
  • Q92.1 - Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
  • Q92.2 - Partial trisomy
  • Q92.5 - Duplications with other complex rearrangements
  • Q92.61 - Marker chromosomes in normal individual
  • Q92.62 - Marker chromosomes in abnormal individual
  • Q92.7 - Triploidy and polyploidy
  • Q92.8 - Other specified trisomies and partial trisomies of autosomes
  • Q92.9 - Trisomy and partial trisomy of autosomes, unspecified
  • Q93.0 - Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)
  • Q93.1 - Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
  • Q93.2 - Chromosome replaced with ring, dicentric or isochromosome
  • Q93.3 - Deletion of short arm of chromosome 4
  • Q93.4 - Deletion of short arm of chromosome 5
  • Q93.51 - Angelman syndrome
  • Q93.52 - Phelan-McDermid syndrome
  • Q93.59 - Other deletions of part of a chromosome
  • Q93.7 - Deletions with other complex rearrangements
  • Q93.81 - Velo-cardio-facial syndrome
  • Q93.82 - Williams syndrome
  • Q93.88 - Other microdeletions
  • Q93.89 - Other deletions from the autosomes
  • Q93.9 - Deletion from autosomes, unspecified
  • Q95.0 - Balanced translocation and insertion in normal individual
  • Q95.1 - Chromosome inversion in normal individual
  • Q95.2 - Balanced autosomal rearrangement in abnormal individual
  • Q95.3 - Balanced sex/autosomal rearrangement in abnormal individual
  • Q95.5 - Individual with autosomal fragile site
  • Q95.8 - Other balanced rearrangements and structural markers
  • Q95.9 - Balanced rearrangement and structural marker, unspecified
  • Q96.0 - Karyotype 45, X
  • Q96.1 - Karyotype 46, X iso (Xq)
  • Q96.2 - Karyotype 46, X with abnormal sex chromosome, except iso (Xq)
  • Q96.3 - Mosaicism, 45, X/46, XX or XY
  • Q96.4 - Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome
  • Q96.8 - Other variants of Turner's syndrome
  • Q96.9 - Turner's syndrome, unspecified
  • Q97.0 - Karyotype 47, XXX
  • Q97.1 - Female with more than three X chromosomes
  • Q97.2 - Mosaicism, lines with various numbers of X chromosomes
  • Q97.3 - Female with 46, XY karyotype
  • Q97.8 - Other specified sex chromosome abnormalities, female phenotype
  • Q97.9 - Sex chromosome abnormality, female phenotype, unspecified
  • Q98.0 - Klinefelter syndrome karyotype 47, XXY
  • Q98.1 - Klinefelter syndrome, male with more than two X chromosomes
  • Q98.3 - Other male with 46, XX karyotype
  • Q98.4 - Klinefelter syndrome, unspecified
  • Q98.5 - Karyotype 47, XYY
  • Q98.6 - Male with structurally abnormal sex chromosome
  • Q98.7 - Male with sex chromosome mosaicism
  • Q98.8 - Other specified sex chromosome abnormalities, male phenotype
  • Q98.9 - Sex chromosome abnormality, male phenotype, unspecified
  • Q99.0 - Chimera 46, XX/46, XY
  • Q99.1 - 46, XX true hermaphrodite
  • Q99.2 - Fragile X chromosome
  • Q99.8 - Other specified chromosome abnormalities
  • Q99.9 - Chromosomal abnormality, unspecified
  • R00.0 - Tachycardia, unspecified
  • R00.1 - Bradycardia, unspecified
  • R00.2 - Palpitations
  • R00.8 - Other abnormalities of heart beat
  • R00.9 - Unspecified abnormalities of heart beat
  • R01.0 - Benign and innocent cardiac murmurs
  • R01.1 - Cardiac murmur, unspecified
  • R01.2 - Other cardiac sounds
  • R03.0 - Elevated blood-pressure reading, without diagnosis of hypertension
  • R03.1 - Nonspecific low blood-pressure reading
  • R04.0 - Epistaxis
  • R04.1 - Hemorrhage from throat
  • R04.2 - Hemoptysis
  • R04.81 - Acute idiopathic pulmonary hemorrhage in infants
  • R04.89 - Hemorrhage from other sites in respiratory passages
  • R04.9 - Hemorrhage from respiratory passages, unspecified
  • R05.1 - Acute cough
  • R05.2 - Subacute cough
  • R05.3 - Chronic cough
  • R05.4 - Cough syncope
  • R05.8 - Other specified cough
  • R05.9 - Cough, unspecified
  • R06.00 - Dyspnea, unspecified
  • R06.01 - Orthopnea
  • R06.02 - Shortness of breath