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ALL MEDICAL CODES IN CATEGORY Congenital malformations
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 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 Q04.9
Congenital malformation of the brain, unspecified.
2025 ICD-10-CM code Q91
Trisomy 18 and Trisomy 13
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 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 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 Q10.1
Congenital ectropion, a condition where the eyelid is turned outward.
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 Q37.9
Unspecified cleft palate with unilateral cleft lip.
2025 ICD-10-CM code Q62.60
Malposition of the ureter, unspecified.
2025 ICD-10-CM code Q20.9
Unspecified congenital malformation of cardiac chambers and connections.
2025 ICD-10-CM code Q21.0
Ventricular septal defect (VSD), a hole in the wall between the heart's ventricles.
2025 ICD-10-CM code Q72.30
Congenital absence of unspecified foot and toe(s).
2025 ICD-10-CM code Q68
Other congenital musculoskeletal deformities, excluding reduction defects of limbs and congenital myotonic chondrodystrophy.
2025 ICD-10-CM code Q38.3
This code signifies other congenital malformations of the tongue, excluding specific conditions like ankyloglossia or macroglossia.
2025 ICD-10-CM code Q71.22
Congenital absence of both forearm and hand on the left upper limb.
2025 ICD-10-CM code Q04.0
Congenital malformations of the corpus callosum, also known as agenesis of the corpus callosum.
2025 ICD-10-CM code Q85.1
Tuberous sclerosis, also known as Bourneville's disease or epiloia, is a genetic disorder characterized by the development of benign tumors in various organs.
2025 ICD-10-CM code Q62.6
Malposition of the ureter.
2025 ICD-10-CM code Q51.828
Other congenital malformations of the cervix.
2025 ICD-10-CM code Q69.0
Accessory finger(s) is an ICD-10-CM code representing the presence of extra fingers.
2025 ICD-10-CM code Q13.1
Absence of iris (Aniridia). Use additional code for associated glaucoma (H42).
2025 ICD-10-CM code Q51.0
Agenesis and aplasia of the uterus; congenital absence of the uterus.
2025 ICD-10-CM code Q50.02
Congenital absence of both ovaries.
2025 ICD-10-CM code Q83.3
Accessory nipple, also known as a supernumerary nipple, is an extra nipple that develops along the milk line during embryonic development.
2025 ICD-10-CM code Q20.4
Double inlet ventricle; a congenital heart defect where both atria connect to a single ventricle.
2025 ICD-10-CM code Q23.0
Congenital stenosis of the aortic valve, a narrowing of the aortic valve present at birth.
2025 ICD-10-CM code Q64.1
Exstrophy of the urinary bladder.
2025 ICD-10-CM code Q82.3
Incontinentia pigmenti is a rare, X-linked dominant genetic disorder primarily affecting females, characterized by skin lesions following Blaschko's lines, and potentially affecting teeth, hair, nails, eyes, and the central nervous system.
2025 ICD-10-CM code Q71.0
Congenital complete absence of an upper limb.
2025 ICD-10-CM code Q67.4
Other congenital deformities of the skull, face, and jaw.
2025 ICD-10-CM code Q04.2
Holoprosencephaly is a rare birth defect affecting brain development.
2025 ICD-10-CM code Q40.0
Congenital hypertrophic pyloric stenosis, a narrowing of the pylorus (the opening between the stomach and small intestine) in infants, caused by muscle thickening.
2025 ICD-10-CM code Q14.9
Congenital malformation of the posterior segment of the eye, unspecified.
2025 ICD-10-CM code Q62.10
Congenital occlusion of the ureter, unspecified.
2025 ICD-10-CM code Q71.9
Unspecified reduction defect of the upper limb.
2025 ICD-10-CM code Q86
Congenital malformation syndromes due to known exogenous causes, not elsewhere classified.
2025 ICD-10-CM code Q17.5
Prominent ear, also known as bat ear.
2025 ICD-10-CM code Q24
Other congenital malformations of heart
2025 ICD-10-CM code Q17.1
Macrotia is a congenital condition characterized by abnormally large ears.
2025 ICD-10-CM code Q87.43
Marfan syndrome with skeletal manifestations.
2025 ICD-10-CM code Q72
Reduction defects of the lower limb.
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