Billable/Specific ICD-10-CM Codes - Page 207

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.

  • Q72.01 - Congenital complete absence of right lower limb
  • Q72.02 - Congenital complete absence of left lower limb
  • Q72.03 - Congenital complete absence of lower limb, bilateral
  • Q72.10 - Congenital absence of unspecified thigh and lower leg with foot present
  • Q72.11 - Congenital absence of right thigh and lower leg with foot present
  • Q72.12 - Congenital absence of left thigh and lower leg with foot present
  • Q72.13 - Congenital absence of thigh and lower leg with foot present, bilateral
  • Q72.20 - Congenital absence of both lower leg and foot, unspecified lower limb
  • Q72.21 - Congenital absence of both lower leg and foot, right lower limb
  • Q72.22 - Congenital absence of both lower leg and foot, left lower limb
  • Q72.23 - Congenital absence of both lower leg and foot, bilateral
  • Q72.30 - Congenital absence of unspecified foot and toe(s)
  • Q72.31 - Congenital absence of right foot and toe(s)
  • Q72.32 - Congenital absence of left foot and toe(s)
  • Q72.33 - Congenital absence of foot and toe(s), bilateral
  • Q72.40 - Longitudinal reduction defect of unspecified femur
  • Q72.41 - Longitudinal reduction defect of right femur
  • Q72.42 - Longitudinal reduction defect of left femur
  • Q72.43 - Longitudinal reduction defect of femur, bilateral
  • Q72.50 - Longitudinal reduction defect of unspecified tibia
  • Q72.51 - Longitudinal reduction defect of right tibia
  • Q72.52 - Longitudinal reduction defect of left tibia
  • Q72.53 - Longitudinal reduction defect of tibia, bilateral
  • Q72.60 - Longitudinal reduction defect of unspecified fibula
  • Q72.61 - Longitudinal reduction defect of right fibula
  • Q72.62 - Longitudinal reduction defect of left fibula
  • Q72.63 - Longitudinal reduction defect of fibula, bilateral
  • Q72.70 - Split foot, unspecified lower limb
  • Q72.71 - Split foot, right lower limb
  • Q72.72 - Split foot, left lower limb
  • Q72.73 - Split foot, bilateral
  • Q72.811 - Congenital shortening of right lower limb
  • Q72.812 - Congenital shortening of left lower limb
  • Q72.813 - Congenital shortening of lower limb, bilateral
  • Q72.819 - Congenital shortening of unspecified lower limb
  • Q72.891 - Other reduction defects of right lower limb
  • Q72.892 - Other reduction defects of left lower limb
  • Q72.893 - Other reduction defects of lower limb, bilateral
  • Q72.899 - Other reduction defects of unspecified lower limb
  • Q72.90 - Unspecified reduction defect of unspecified lower limb
  • Q72.91 - Unspecified reduction defect of right lower limb
  • Q72.92 - Unspecified reduction defect of left lower limb
  • Q72.93 - Unspecified reduction defect of lower limb, bilateral
  • Q73.0 - Congenital absence of unspecified limb(s)
  • Q73.1 - Phocomelia, unspecified limb(s)
  • Q73.8 - Other reduction defects of unspecified limb(s)
  • Q74.0 - Other congenital malformations of upper limb(s), including shoulder girdle
  • Q74.1 - Congenital malformation of knee
  • Q74.2 - Other congenital malformations of lower limb(s), including pelvic girdle
  • Q74.3 - Arthrogryposis multiplex congenita
  • Q74.8 - Other specified congenital malformations of limb(s)
  • Q74.9 - Unspecified congenital malformation of limb(s)
  • Q75.001 - Craniosynostosis unspecified, unilateral
  • Q75.002 - Craniosynostosis unspecified, bilateral
  • Q75.009 - Craniosynostosis unspecified
  • Q75.01 - Sagittal craniosynostosis
  • Q75.021 - Coronal craniosynostosis unilateral
  • Q75.022 - Coronal craniosynostosis bilateral
  • Q75.029 - Coronal craniosynostosis unspecified
  • Q75.03 - Metopic craniosynostosis
  • Q75.041 - Lambdoid craniosynostosis, unilateral
  • Q75.042 - Lambdoid craniosynostosis, bilateral
  • Q75.049 - Lambdoid craniosynostosis, unspecified
  • Q75.051 - Cloverleaf skull
  • Q75.052 - Pansynostosis
  • Q75.058 - Other multi-suture craniosynostosis
  • Q75.08 - Other single-suture craniosynostosis
  • Q75.1 - Craniofacial dysostosis
  • Q75.2 - Hypertelorism
  • Q75.3 - Macrocephaly
  • Q75.4 - Mandibulofacial dysostosis
  • Q75.5 - Oculomandibular dysostosis
  • Q75.8 - Other specified congenital malformations of skull and face bones
  • Q75.9 - Congenital malformation of skull and face bones, unspecified
  • Q76.0 - Spina bifida occulta
  • Q76.1 - Klippel-Feil syndrome
  • Q76.2 - Congenital spondylolisthesis
  • Q76.3 - Congenital scoliosis due to congenital bony malformation
  • Q76.411 - Congenital kyphosis, occipito-atlanto-axial region
  • Q76.412 - Congenital kyphosis, cervical region
  • Q76.413 - Congenital kyphosis, cervicothoracic region
  • Q76.414 - Congenital kyphosis, thoracic region
  • Q76.415 - Congenital kyphosis, thoracolumbar region
  • Q76.419 - Congenital kyphosis, unspecified region
  • Q76.425 - Congenital lordosis, thoracolumbar region
  • Q76.426 - Congenital lordosis, lumbar region
  • Q76.427 - Congenital lordosis, lumbosacral region
  • Q76.428 - Congenital lordosis, sacral and sacrococcygeal region
  • Q76.429 - Congenital lordosis, unspecified region
  • Q76.49 - Other congenital malformations of spine, not associated with scoliosis
  • Q76.5 - Cervical rib
  • Q76.6 - Other congenital malformations of ribs
  • Q76.7 - Congenital malformation of sternum
  • Q76.8 - Other congenital malformations of bony thorax
  • Q76.9 - Congenital malformation of bony thorax, unspecified
  • Q77.0 - Achondrogenesis
  • Q77.1 - Thanatophoric short stature
  • Q77.2 - Short rib syndrome
  • Q77.3 - Chondrodysplasia punctata
  • Q77.4 - Achondroplasia