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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 Q66.82
Congenital vertical talus deformity affecting the left foot.
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 Q72.32
Congenital absence of the left foot and toes.
2025 ICD-10-CM code Q27.30
Arteriovenous malformation, site unspecified; an abnormal connection between arteries and veins.
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 Q40.9
Congenital malformation of the upper alimentary tract, unspecified.
2025 ICD-10-CM code Q82.0
Hereditary lymphedema. This condition is a congenital disorder characterized by swelling due to impaired lymphatic drainage.
2025 ICD-10-CM code Q03
Congenital hydrocephalus. This condition refers to the accumulation of cerebrospinal fluid in the brain that is present at birth.
2025 ICD-10-CM code Q72.03
Congenital complete absence of lower limb, bilateral.
2025 ICD-10-CM code Q55.0
Absence and aplasia of testis (monorchism).
2025 ICD-10-CM code Q65.82
Congenital coxa vara. This is a birth defect affecting the hip joint, where the angle between the head and neck of the femur and its shaft is reduced.
2025 ICD-10-CM code Q98.3
This code represents a male individual with a 46, XX karyotype, a condition where a male has two X chromosomes instead of one X and one Y chromosome.
2025 ICD-10-CM code Q72.53
Bilateral longitudinal reduction defect of the tibia.
Alport syndrome, a rare genetic disorder affecting the kidneys, ears, and eyes.
2025 ICD-10-CM code Q89
Other congenital malformations, not elsewhere classified.
2025 ICD-10-CM code Q52.11
Transverse vaginal septum is a congenital malformation characterized by a complete or partial blockage of the vagina.
2025 ICD-10-CM code Q71.811
Congenital shortening of the right upper limb.
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