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ALL MEDICAL CODES IN CATEGORY Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)

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 Q78.3

Progressive diaphyseal dysplasia (Camurati-Engelmann syndrome)

2025 ICD-10-CM code Q33.3

Congenital agenesis of lung (lobe).

2025 ICD-10-CM code Q17.1

Macrotia is a congenital condition characterized by abnormally large ears.

2025 ICD-10-CM code Q69

Polydactyly, a congenital condition characterized by the presence of extra fingers or toes.

2025 ICD-10-CM code Q79.69

Other Ehlers-Danlos syndromes.This code is used to classify various forms of Ehlers-Danlos syndrome not otherwise specified.

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 Q77.7

Spondyloepiphyseal dysplasia is a genetic disorder affecting bone and cartilage development, resulting in skeletal abnormalities.

2025 ICD-10-CM code Q66.50

Congenital pes planus (flat feet) of unspecified foot.

2025 ICD-10-CM code Q05.5

Cervical spina bifida without hydrocephalus.

2025 ICD-10-CM code Q65.6

Congenital unstable hip; also known as congenital dislocatable hip.

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 Q76.427

Congenital lordosis in the lumbosacral region.

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 Q70.01

Fused fingers on the right hand.

2025 ICD-10-CM code Q99.9

This code represents an unspecified chromosomal abnormality.

2025 ICD-10-CM code Q93.4

Deletion of the short arm of chromosome 5, also known as Cri-du-chat syndrome.

2025 ICD-10-CM code Q39.5

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

2025 ICD-10-CM code Q70.9

Syndactyly, unspecified; fusion of fingers or toes.

2025 ICD-10-CM code Q76.411

Congenital kyphosis affecting the occipito-atlanto-axial region.

2025 ICD-10-CM code Q76.429

Congenital lordosis, unspecified region.

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 Q98.5

Karyotype 47, XYY is a chromosomal abnormality characterized by an extra Y chromosome.

2025 ICD-10-CM code Q55.61

Curvature of the penis (lateral).

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 Q61.19

Other polycystic kidney, infantile type. This code is used to classify a specific type of polycystic kidney disease in infants.

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 Q25.45

Double aortic arch, also known as a vascular ring of the aorta.

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 Q72.31

Congenital absence of the right foot and toes.

2025 ICD-10-CM code Q74.3

Arthrogryposis multiplex congenita (AMC) is a group of disorders characterized by congenital contractures in multiple joints, usually present at birth.

2025 ICD-10-CM code Q93.9

Deletion from autosomes, unspecified.

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