Non-Billable/Non-Specific ICD-10-CM Codes - Page 48

There are 8,831 ICD-10-CM codes which are non-billable/non-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.

  • Q50.0 - Congenital absence of ovary
  • Q50.3 - Other congenital malformations of ovary
  • Q51.1 - Doubling of uterus with doubling of cervix and vagina
  • Q51.2 - Other doubling of uterus
  • Q51.8 - Other congenital malformations of uterus and cervix
  • Q51.81 - Other congenital malformations of uterus
  • Q51.82 - Other congenital malformations of cervix
  • Q52.1 - Doubling of vagina
  • Q52.12 - Longitudinal vaginal septum
  • Q52.7 - Other and unspecified congenital malformations of vulva
  • Q53.0 - Ectopic testis
  • Q53.1 - Undescended testicle, unilateral
  • Q53.11 - Abdominal testis, unilateral
  • Q53.2 - Undescended testicle, bilateral
  • Q53.21 - Abdominal testis, bilateral
  • Q55.2 - Other and unspecified congenital malformations of testis and scrotum
  • Q55.6 - Other congenital malformations of penis
  • Q61.0 - Congenital renal cyst
  • Q61.1 - Polycystic kidney, infantile type
  • Q62.1 - Congenital occlusion of ureter
  • Q62.3 - Other obstructive defects of renal pelvis and ureter
  • Q62.6 - Malposition of ureter
  • Q64.1 - Exstrophy of urinary bladder
  • Q64.3 - Other atresia and stenosis of urethra and bladder neck
  • Q64.7 - Other and unspecified congenital malformations of bladder and urethra
  • Q65.0 - Congenital dislocation of hip, unilateral
  • Q65.3 - Congenital partial dislocation of hip, unilateral
  • Q65.8 - Other congenital deformities of hip
  • Q66.0 - Congenital talipes equinovarus
  • Q66.1 - Congenital talipes calcaneovarus
  • Q66.2 - Congenital metatarsus (primus) varus
  • Q66.21 - Congenital metatarsus primus varus
  • Q66.22 - Congenital metatarsus adductus
  • Q66.3 - Other congenital varus deformities of feet
  • Q66.4 - Congenital talipes calcaneovalgus
  • Q66.5 - Congenital pes planus
  • Q66.7 - Congenital pes cavus
  • Q66.8 - Other congenital deformities of feet
  • Q66.9 - Congenital deformity of feet, unspecified
  • Q70.0 - Fused fingers
  • Q70.1 - Webbed fingers
  • Q70.2 - Fused toes
  • Q70.3 - Webbed toes
  • Q71.0 - Congenital complete absence of upper limb
  • Q71.1 - Congenital absence of upper arm and forearm with hand present
  • Q71.2 - Congenital absence of both forearm and hand
  • Q71.3 - Congenital absence of hand and finger
  • Q71.4 - Longitudinal reduction defect of radius
  • Q71.5 - Longitudinal reduction defect of ulna
  • Q71.6 - Lobster-claw hand
  • Q71.8 - Other reduction defects of upper limb
  • Q71.81 - Congenital shortening of upper limb
  • Q71.89 - Other reduction defects of upper limb
  • Q71.9 - Unspecified reduction defect of upper limb
  • Q72.0 - Congenital complete absence of lower limb
  • Q72.1 - Congenital absence of thigh and lower leg with foot present
  • Q72.2 - Congenital absence of both lower leg and foot
  • Q72.3 - Congenital absence of foot and toe(s)
  • Q72.4 - Longitudinal reduction defect of femur
  • Q72.5 - Longitudinal reduction defect of tibia
  • Q72.6 - Longitudinal reduction defect of fibula
  • Q72.7 - Split foot
  • Q72.8 - Other reduction defects of lower limb
  • Q72.81 - Congenital shortening of lower limb
  • Q72.89 - Other reduction defects of lower limb
  • Q72.9 - Unspecified reduction defect of lower limb
  • Q75.0 - Craniosynostosis
  • Q75.00 - Craniosynostosis unspecified
  • Q75.02 - Coronal craniosynostosis
  • Q75.04 - Lambdoid craniosynostosis
  • Q75.05 - Multi-suture craniosynostosis
  • Q76.4 - Other congenital malformations of spine, not associated with scoliosis
  • Q76.41 - Congenital kyphosis
  • Q76.42 - Congenital lordosis
  • Q79.5 - Other congenital malformations of abdominal wall
  • Q79.6 - Ehlers-Danlos syndromes
  • Q85.0 - Neurofibromatosis (nonmalignant)
  • Q85.8 - Other phakomatoses, not elsewhere classified
  • Q87.1 - Congenital malformation syndromes predominantly associated with short stature
  • Q87.4 - Marfan syndrome
  • Q87.41 - Marfan syndrome with cardiovascular manifestations
  • Q87.8 - Other specified congenital malformation syndromes, not elsewhere classified
  • Q89.0 - Congenital absence and malformations of spleen
  • Q92.6 - Marker chromosomes
  • Q93.5 - Other deletions of part of a chromosome
  • Q93.8 - Other deletions from the autosomes
  • R04.8 - Hemorrhage from other sites in respiratory passages
  • R06.0 - Dyspnea
  • R06.8 - Other abnormalities of breathing
  • R07.8 - Other chest pain
  • R09.0 - Asphyxia and hypoxemia
  • R09.8 - Other specified symptoms and signs involving the circulatory and respiratory systems
  • R09.A - Foreign body sensation of the circulatory and respiratory system
  • R10.1 - Pain localized to upper abdomen
  • R10.3 - Pain localized to other parts of lower abdomen
  • R10.8 - Other abdominal pain
  • R10.81 - Abdominal tenderness
  • R10.82 - Rebound abdominal tenderness
  • R11.1 - Vomiting
  • R13.1 - Dysphagia