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ALL MEDICAL CODES IN CATEGORY Congenital malformations, deformations and chromosomal abnormalities
2025 ICD-10-CM code Q87.11
Prader-Willi syndrome.
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 Q77.7
Spondyloepiphyseal dysplasia is a genetic disorder affecting bone and cartilage development, resulting in skeletal abnormalities.
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 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 Q68.0
Congenital deformity of the sternocleidomastoid muscle, also known as congenital torticollis.
2025 ICD-10-CM code Q69.9
Polydactyly, unspecified; presence of supernumerary digits.
2025 ICD-10-CM code Q37.9
Unspecified cleft palate with unilateral cleft lip.
2025 ICD-10-CM code Q66.82
Congenital vertical talus deformity affecting the left foot.
2025 ICD-10-CM code Q93.81
Velo-cardio-facial syndrome, a chromosomal abnormality.
2025 ICD-10-CM code Q72.12
Congenital absence of the left thigh and lower leg, with the foot present.
2025 ICD-10-CM code Q06.3
Other congenital cauda equina malformations.
2025 ICD-10-CM code Q66.90
Congenital deformity of the feet, unspecified, and unspecified foot.
2025 ICD-10-CM code Q72.32
Congenital absence of the left foot and toes.
2025 ICD-10-CM code Q72.89
Other reduction defects of the lower limb.
2025 ICD-10-CM code Q72.81
Congenital shortening of the lower limb.
2025 ICD-10-CM code Q71.51
Longitudinal reduction defect of the right ulna.
2025 ICD-10-CM code Q98.4
Klinefelter syndrome, unspecified.
2025 ICD-10-CM code Q18.4
Macrostomia.
2025 ICD-10-CM code Q05.0
Cervical spina bifida with hydrocephalus. This condition involves a defect in the closure of the spinal column in the cervical region, accompanied by an excessive accumulation of cerebrospinal fluid in the brain.
2025 ICD-10-CM code Q71.20
Congenital absence of both forearm and hand, unspecified upper limb.
2025 ICD-10-CM code Q33
Congenital malformations of lung. This encompasses various lung malformations present at birth.
2025 ICD-10-CM code Q51.28
Other and unspecified doubling of uterus. This includes conditions like septate uterus NOS where the uterus is partially or completely divided.
2025 ICD-10-CM code Q71.41
Longitudinal reduction defect of right radius. This congenital condition affects the development of the radius bone in the right forearm.
2025 ICD-10-CM code Q76.414
Congenital kyphosis, thoracic region.
2025 ICD-10-CM code Q28.2
Arteriovenous malformation of cerebral vessels. This condition is a congenital abnormality characterized by a tangle of abnormal blood vessels connecting arteries and veins in the brain.
2025 ICD-10-CM code Q37.4
Cleft hard and soft palate with bilateral cleft lip.
2025 ICD-10-CM code Q64.11
Supravesical fissure of urinary bladder. This is a congenital defect where the bladder doesn't fully close at the top.
2025 ICD-10-CM code Q61.3
Polycystic kidney, unspecified.
2025 ICD-10-CM code Q67.1
Congenital compression facies. This condition describes facial deformities caused by compression during fetal development.
2025 ICD-10-CM code Q11
This code encompasses developmental defects of the eye, including absence of the eye (anophthalmos), abnormally small eye (microphthalmos), and abnormally large eye (macrophthalmos).
2025 ICD-10-CM code Q18.3
Webbing of neck (Pterygium colli)
2025 ICD-10-CM code Q99.8
Other specified chromosome abnormalities.
2025 ICD-10-CM code Q43.7
Persistent cloaca. Cloaca NOS.
2025 ICD-10-CM code Q66.02
Congenital talipes equinovarus, left foot.
2025 ICD-10-CM code Q45.2
Congenital pancreatic cyst. This condition is present from birth.
2025 ICD-10-CM code Q35.5
Cleft hard palate with cleft soft palate.
2025 ICD-10-CM code Q01
Encephalocele. Includes: Arnold-Chiari syndrome, type III, encephalocystocele, encephalomyelocele, hydroencephalocele, hydromeningocele, cranial, meningocele, cerebral, meningoencephalocele.
2025 ICD-10-CM code Q10.7
Congenital malformation of orbit.
2025 ICD-10-CM code Q64.4
Malformation of urachus. This includes cyst of urachus, patent urachus, and prolapse of urachus.
2025 ICD-10-CM code Q91.2
Trisomy 18, translocation.
2025 ICD-10-CM code Q83
Congenital malformations of breast
2025 ICD-10-CM code Q71.819
Congenital shortening of unspecified upper limb.
2025 ICD-10-CM code Q34.8
Other specified congenital malformations of respiratory system. This includes conditions like nasopharyngeal atresia.
2025 ICD-10-CM code Q35.7
Cleft uvula.
2025 ICD-10-CM code Q79.3
Gastroschisis.
2025 ICD-10-CM code Q78.1
Polyostotic fibrous dysplasia.This condition is characterized by the replacement of normal bone with fibrous tissue in multiple bones.
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