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

2025 ICD-10-CM code Q78.3

Progressive diaphyseal dysplasia (Camurati-Engelmann syndrome)

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 Q66.50

Congenital pes planus (flat feet) of unspecified foot.

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 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 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 Q76.411

Congenital kyphosis affecting the occipito-atlanto-axial region.

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 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 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 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 Q68.0

Congenital deformity of the sternocleidomastoid muscle, also known as congenital torticollis.

2025 ICD-10-CM code Q55

Other congenital malformations of the male genital organs.

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 Q93.81

Velo-cardio-facial syndrome, a chromosomal abnormality.

2025 ICD-10-CM code Q64.75

Double urinary meatus is a congenital anomaly characterized by the presence of two external urethral openings.

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 Q06.3

Other congenital cauda equina malformations.

2025 ICD-10-CM code Q79.51

Congenital hernia of the bladder.

2025 ICD-10-CM code Q07.8

Other specified congenital malformations of nervous system.

2025 ICD-10-CM code Q43.0

Meckel's diverticulum (displaced) (hypertrophic). Persistent omphalomesenteric duct. Persistent vitelline duct.

2025 ICD-10-CM code Q26.1

Persistent left superior vena cava.

2025 ICD-10-CM code Q87.8

Other specified congenital malformation syndromes, not elsewhere classified.

2025 ICD-10-CM code Q21.8

Other congenital malformations of cardiac septa. This includes conditions like Eisenmenger's defect and Pentalogy of Fallot.

2025 ICD-10-CM code Q17.1

Macrotia is a congenital condition characterized by abnormally large ears.

2025 ICD-10-CM code Q79.61

Classical Ehlers-Danlos syndrome (cEDS) is a genetic disorder affecting connective tissues, resulting in hyperelastic skin, hypermobile joints, and fragile blood vessels.

2025 ICD-10-CM code Q72.0

Congenital complete absence of a lower limb.

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 Q50.2

Congenital torsion of ovary.

2025 ICD-10-CM code Q55.21

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

2025 ICD-10-CM code Q55.23

Scrotal transposition, a congenital condition where the location of the scrotum is abnormal.

2025 ICD-10-CM code Q55.29

Other congenital malformations of testis and scrotum