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ALL MEDICAL CODES IN CATEGORY Congenital malformations of the nervous system

2025 ICD-10-CM code Q05.5

Cervical spina bifida without hydrocephalus.

2025 ICD-10-CM code Q04.9

Congenital malformation of the brain, unspecified.

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 Q04.1

Arhinencephaly, a congenital absence of the olfactory bulbs and olfactory tracts.

2025 ICD-10-CM code Q05.7

Lumbar spina bifida without hydrocephalus.

2025 ICD-10-CM code Q04.4

Septo-optic dysplasia of the brain, a rare congenital disorder characterized by hypoplasia of the optic nerves, midline brain abnormalities, and pituitary gland hypoplasia.

2025 ICD-10-CM code Q06.2

Diastematomyelia is a congenital spinal cord malformation characterized by a longitudinal split in the spinal cord.

2025 ICD-10-CM code Q06.3

Other congenital cauda equina malformations.

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 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 Q01

Encephalocele. Includes: Arnold-Chiari syndrome, type III, encephalocystocele, encephalomyelocele, hydroencephalocele, hydromeningocele, cranial, meningocele, cerebral, meningoencephalocele.

2025 ICD-10-CM code Q00.0

Anencephaly.

2025 ICD-10-CM code Q06.8

Other specified congenital malformations of spinal cord.

2025 ICD-10-CM code Q03.9

Congenital hydrocephalus, unspecified.

2025 ICD-10-CM code Q01.8

Encephalocele of other sites. This condition involves a protrusion of brain tissue and meninges through a defect in the skull, occurring in locations other than the frontal or occipital regions.

2025 ICD-10-CM code Q05.3

Sacral spina bifida with hydrocephalus.

2025 ICD-10-CM code Q01.9

Encephalocele, unspecified: A protrusion of brain tissue through a skull opening.

2025 ICD-10-CM code Q06.1

Hypoplasia and dysplasia of the spinal cord.

2025 ICD-10-CM code Q05.2

Lumbar spina bifida with hydrocephalus; also includes lumbosacral spina bifida with hydrocephalus.

2025 ICD-10-CM code Q06.0

Amyelia, a congenital malformation characterized by the absence of a portion of the spinal cord.

2025 ICD-10-CM code Q07.02

Arnold-Chiari syndrome with hydrocephalus.

2025 ICD-10-CM code Q03.8

Other congenital hydrocephalus. This condition involves enlarged cerebrospinal fluid cavities in the head present from birth.

2025 ICD-10-CM code Q05

Spina bifida is a birth defect where the spine doesn't fully close during pregnancy. This can cause a range of physical disabilities.

2025 ICD-10-CM code Q00

Anencephaly and similar malformations.

2025 ICD-10-CM code Q07.01

Arnold-Chiari syndrome with spina bifida.

2025 ICD-10-CM code Q07.9

Congenital malformation of the nervous system, unspecified.

2025 ICD-10-CM code Q06

Other congenital malformations of spinal cord.

2025 ICD-10-CM code Q04.3

Reduction deformities of the brain, characterized by the absence or incomplete development of brain parts.

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 Q05.4

Unspecified spina bifida with hydrocephalus.

2025 ICD-10-CM code Q05.8

Sacral spina bifida without hydrocephalus.

2025 ICD-10-CM code Q01.2

Occipital encephalocele. This is a birth defect where part of the brain protrudes through an opening in the back of the skull.

2025 ICD-10-CM code Q04.6

Congenital cerebral cysts. This encompasses conditions like porencephaly and schizencephaly.

2025 ICD-10-CM code Q07.03

Arnold-Chiari syndrome with spina bifida and hydrocephalus.

2025 ICD-10-CM code Q01.1

Nasofrontal encephalocele; a protrusion of brain tissue through a defect in the skull at the fronto-nasal junction.

2025 ICD-10-CM code Q04.5

Megalencephaly is a condition characterized by an abnormally large brain size, typically diagnosed at birth or during early childhood, often leading to developmental delays and neurological issues.

2025 ICD-10-CM code Q00.1

Craniorachischisis is a severe congenital malformation where the brain and spinal cord are open.

2025 ICD-10-CM code Q00.2

Iniencephaly is a rare birth defect characterized by defects in the occipital bone, cervical vertebrae, and retroflexion of the head.

2025 ICD-10-CM code Q04.2

Holoprosencephaly is a rare birth defect affecting brain development.

2025 ICD-10-CM code Q07.0

Arnold-Chiari syndrome. This is a congenital malformation where parts of the cerebellum are displaced.

2025 ICD-10-CM code Q07.8

Other specified congenital malformations of nervous system.

2025 ICD-10-CM code Q02

Microcephaly. Codefirst, if applicable, congenital Zika virus disease.

2025 ICD-10-CM code Q06.4

Hydromyelia (excess cerebrospinal fluid within the spinal cord's central canal).

2025 ICD-10-CM code Q05.9

Spina bifida, unspecified.

2025 ICD-10-CM code Q05.6

Thoracic spina bifida without hydrocephalus.

2025 ICD-10-CM code Q03.0

Malformations of aqueduct of Sylvius. This includes anomaly, obstruction, or stenosis of the aqueduct.

2025 ICD-10-CM code Q03.1

Atresia of foramina of Magendie and Luschka (Dandy-Walker syndrome).

2025 ICD-10-CM code Q07.00

Arnold-Chiari syndrome without spina bifida or hydrocephalus.

2025 ICD-10-CM code Q05.1

Thoracic spina bifida with hydrocephalus.

2025 ICD-10-CM code Q04.8

This ICD-10-CM code classifies other specified congenital malformations of the brain, excluding conditions like cyclopia and macrocephaly.

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