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ALL MEDICAL CODES IN CATEGORY Q00-Q99

2025 ICD-10-CM code Q22.1

Congenital pulmonary valve stenosis.

2025 ICD-10-CM code Q18.4

Macrostomia.

2025 ICD-10-CM code Q92.61

Marker chromosomes in normal individual. This condition involves the presence of small, extra chromosomes called marker chromosomes, which are typically seen in individuals with a normal phenotype.

2025 ICD-10-CM code Q05.0

Cervical spina bifida with hydrocephalus. This condition involves a defect in the closure of the spinal column in the cervical region, accompanied by an excessive accumulation of cerebrospinal fluid in the brain.

2025 ICD-10-CM code Q70.10

Webbed fingers, unspecified hand.

2025 ICD-10-CM code Q72.01

Congenital complete absence of right lower limb.

2025 ICD-10-CM code Q07.02

Arnold-Chiari syndrome with hydrocephalus.

2025 ICD-10-CM code Q72.813

Congenital shortening of lower limb, bilateral.

2025 ICD-10-CM code Q17.4

Misplaced ear. Low-set ears.

2025 ICD-10-CM code Q51.28

Other and unspecified doubling of uterus. This includes conditions like septate uterus NOS where the uterus is partially or completely divided.

2025 ICD-10-CM code Q70

Syndactyly (fusion of fingers or toes).

2025 ICD-10-CM code Q71.41

Longitudinal reduction defect of right radius. This congenital condition affects the development of the radius bone in the right forearm.

2025 ICD-10-CM code Q66.1

Congenital talipes calcaneovarus. This is a birth defect where the foot is twisted out of shape or position.

2025 ICD-10-CM code Q50.32

Ovarian streak, 46,XX with streak gonads.

2025 ICD-10-CM code Q72.43

This code describes a longitudinal reduction defect of the femur, bilaterally.

2025 ICD-10-CM code Q76.414

Congenital kyphosis, thoracic region.

2025 ICD-10-CM code Q28.2

Arteriovenous malformation of cerebral vessels. This condition is a congenital abnormality characterized by a tangle of abnormal blood vessels connecting arteries and veins in the brain.

2025 ICD-10-CM code Q51

Congenital malformations of the uterus and cervix.

2025 ICD-10-CM code Q64.11

Supravesical fissure of urinary bladder. This is a congenital defect where the bladder doesn't fully close at the top.

2025 ICD-10-CM code Q72.92

Unspecified reduction defect of the left lower limb. This condition is a congenital anomaly characterized by the incomplete development of the left lower limb.

2025 ICD-10-CM code Q30.0

Choanal atresia. This is a congenital blockage of the nasal passages, usually by bone or membrane.

2025 ICD-10-CM code Q18.3

Webbing of neck (Pterygium colli)

2025 ICD-10-CM code Q66.42

Congenital talipes calcaneovalgus, left foot.

2025 ICD-10-CM code Q26.6

Portal vein-hepatic artery fistula. This is a congenital abnormality where there is an abnormal connection between the portal vein and the hepatic artery.

2025 ICD-10-CM code Q16.3

Congenital malformation of ear ossicles. This includes congenital fusion of ear ossicles.

2025 ICD-10-CM code Q50.1

This code represents a developmental ovarian cyst, a congenital condition.

2025 ICD-10-CM code Q95.5

Individual with autosomal fragile site.

2025 ICD-10-CM code Q61.2

Polycystic kidney, adult type (also known as autosomal dominant polycystic kidney disease).

2025 ICD-10-CM code Q87.410

Marfan syndrome with aortic dilation.

2025 ICD-10-CM code Q10.7

Congenital malformation of orbit.

2025 ICD-10-CM code Q53.13

Unilateral high scrotal testis. This condition refers to an undescended testicle that is located higher in the scrotum than is typical.

2025 ICD-10-CM code Q51.1

Doubling of uterus with doubling of cervix and vagina. This condition involves a congenital duplication of both the uterus and cervix.

2025 ICD-10-CM code Q66.221

Congenital metatarsus adductus, right foot.

2025 ICD-10-CM code Q64.4

Malformation of urachus. This includes cyst of urachus, patent urachus, and prolapse of urachus.

2025 ICD-10-CM code Q71.819

Congenital shortening of unspecified upper limb.

2025 ICD-10-CM code Q34.8

Other specified congenital malformations of respiratory system. This includes conditions like nasopharyngeal atresia.

2025 ICD-10-CM code Q87.2

Congenital malformation syndromes predominantly involving limbs.

2025 ICD-10-CM code Q51.8

Other congenital malformations of uterus and cervix.

2025 ICD-10-CM code Q89.9

Congenital malformation, unspecified.

2025 ICD-10-CM code Q82.6

Congenital sacral dimple. This is a minor congenital malformation characterized by a small dimple or pit in the skin at the base of the spine, in the sacral area. 

2025 ICD-10-CM code Q79.3

Gastroschisis.

2025 ICD-10-CM code Q71.43

Longitudinal reduction defect of the radius, bilaterally.

2025 ICD-10-CM code Q36.9

Cleft lip, unilateral. Cleft lip NOS.

2025 ICD-10-CM code Q79.59

Other congenital malformations of abdominal wall.

2025 ICD-10-CM code Q50.0

Congenital absence of ovary.

2025 ICD-10-CM code Q27.34

Arteriovenous malformation of renal vessel. This is a congenital condition where there is an abnormal tangle of blood vessels connecting arteries and veins in the kidney, disrupting normal blood flow and oxygen circulation.

2025 ICD-10-CM code Q63

Other congenital malformations of kidney

2025 ICD-10-CM code Q75.0

Craniosynostosis. This is a birth defect where the bones in a baby's skull join together too early.

2025 ICD-10-CM code Q64.79

Other congenital malformations of bladder and urethra

2025 ICD-10-CM code Q53.9

Undescended testicle, unspecified. Cryptorchism NOS.