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ALL MEDICAL CODES IN CATEGORY Congenital malformations

2025 ICD-10-CM code Q55.64

Hidden penis, also known as buried penis or concealed penis.

2025 ICD-10-CM code Q31.3

Laryngocele, a congenital dilatation of the laryngeal saccule.

2025 ICD-10-CM code Q17.1

Macrotia is a congenital condition characterized by abnormally large ears.

2025 ICD-10-CM code Q31.5

Congenital laryngomalacia is a condition present at birth where the soft tissues above the voice box are weak and floppy, causing noisy breathing (stridor).

2025 ICD-10-CM code Q43.5

Ectopic anus is a congenital malformation where the anus is not in its normal anatomical position.

2025 ICD-10-CM code Q66.50

Congenital pes planus (flat feet) of unspecified foot.

2025 ICD-10-CM code Q30

Congenital malformations of the nose.

2025 ICD-10-CM code Q33.4

Congenital bronchiectasis is a condition where the bronchi (airways in the lungs) are abnormally widened, present from birth.

2025 ICD-10-CM code Q63.0

Accessory kidney is a congenital anomaly characterized by the presence of an extra kidney.

2025 ICD-10-CM code Q04.9

Congenital malformation of the brain, unspecified.

2025 ICD-10-CM code Q85.8

Other phakomatoses, not elsewhere classified.

2025 ICD-10-CM code Q70.4

Polysyndactyly, unspecified.This code is used for cases of multiple supernumerary digits or fused digits without specifying the location or type.

2025 ICD-10-CM code Q12.3

Congenital aphakia is the absence of the eye lens at birth.

2025 ICD-10-CM code Q86.1

Fetal hydantoin syndrome, also known as Meadow's syndrome, is a group of birth defects caused by exposure to anticonvulsant drugs during pregnancy.

2025 ICD-10-CM code Q91

Trisomy 18 and Trisomy 13

2025 ICD-10-CM code Q87.81

Alport syndrome, a rare genetic disorder affecting the kidneys, ears, and eyes.

2025 ICD-10-CM code Q95.0

Balanced translocation and insertion in a normal individual.

2025 ICD-10-CM code Q39.5

Congenital dilatation of the esophagus; also known as congenital cardiospasm.

2025 ICD-10-CM code Q23.2

Congenital mitral stenosis; a narrowing of the mitral valve present at birth.

2025 ICD-10-CM code Q43.1

Hirschsprung's disease, also known as aganglionic megacolon, is a congenital condition characterized by the absence of ganglion cells in a segment of the bowel, leading to intestinal obstruction.

2025 ICD-10-CM code Q10.5

Congenital stenosis and stricture of the lacrimal duct.

2025 ICD-10-CM code Q87.43

Marfan syndrome with skeletal manifestations.

2025 ICD-10-CM code Q61.1

Polycystic kidney, infantile type.This code describes a rare, inherited kidney disorder characterized by multiple cysts in the kidneys.

2025 ICD-10-CM code Q01.0

Frontal encephalocele, a congenital neural tube defect where brain tissue protrudes through a skull opening in the frontal region.

2025 ICD-10-CM code Q89

Other congenital malformations, not elsewhere classified.

2025 ICD-10-CM code Q71.23

Congenital absence of both forearms and hands, bilaterally.

2025 ICD-10-CM code Q90

Down syndrome, a chromosomal abnormality characterized by an extra copy of chromosome 21.

2025 ICD-10-CM code Q77.9

Osteochondrodysplasia with defects in the growth of tubular bones and spine, unspecified.

2025 ICD-10-CM code Q42

Congenital absence, atresia, and stenosis of the large intestine.

2025 ICD-10-CM code Q76

Congenital malformations of the spine and bony thorax.

2025 ICD-10-CM code Q22.8

Other congenital malformations of the tricuspid valve.

2025 ICD-10-CM code Q10.1

Congenital ectropion, a condition where the eyelid is turned outward.

2025 ICD-10-CM code Q36

Cleft lip, a congenital fissure of the lip.

2025 ICD-10-CM code Q64.0

Epispadias is a congenital defect where the urethra opens on the upper surface of the penis.

2025 ICD-10-CM code Q72.13

Congenital absence of thigh and lower leg with foot present, bilateral.

2025 ICD-10-CM code Q55

Other congenital malformations of the male genital organs.

2025 ICD-10-CM code Q72.53

Bilateral longitudinal reduction defect of the tibia.

2025 ICD-10-CM code Q04

Other congenital malformations of the brain.

2025 ICD-10-CM code Q56.3

Pseudohermaphroditism, unspecified.This code is used when a person is born with ambiguous genitalia, and the specific type of pseudohermaphroditism cannot be determined.

2025 ICD-10-CM code Q04.1

Arhinencephaly, a congenital absence of the olfactory bulbs and olfactory tracts.

2025 ICD-10-CM code Q83.2

Absent nipple, a congenital condition present at birth.

2025 ICD-10-CM code Q37.9

Unspecified cleft palate with unilateral cleft lip.

2025 ICD-10-CM code Q72.21

Congenital absence of both lower leg and foot on the right lower limb.

2025 ICD-10-CM code Q11.1

Other anophthalmos; absence of one or both eyes.

2025 ICD-10-CM code Q64.73

Congenital urethrorectal fistula is a birth defect where an abnormal connection exists between the urethra and rectum.

2025 ICD-10-CM code Q97.2

Mosaicism, lines with various numbers of X chromosomes.This is a congenital disorder involving variations in the number of X chromosomes across different cells in the body.

2025 ICD-10-CM code Q81.9

Epidermolysis bullosa, unspecified; a group of inherited skin disorders causing blistering.

2025 ICD-10-CM code Q62.60

Malposition of the ureter, unspecified.

2025 ICD-10-CM code Q05.7

Lumbar spina bifida without hydrocephalus.

2025 ICD-10-CM code Q55.21

Polyorchism is a congenital anomaly characterized by the presence of more than two testes.