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