AutoICD API

Q04.0

Billable

Congenital malformations of corpus callosum

Congenital malformations of corpus callosum

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Agenesis of corpus callosum

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(8)
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(191)

SNOMED CT

UMLS

Clinical Terms

  • Cleft iris
  • Agenesis corpus callosum
  • Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome
  • Disorder of serine metabolism
  • ASCT1 deficiency
  • Corpus callosum agenesis, abnormal genitalia syndrome
  • Temtamy syndrome
  • ACC
  • Congenital malformation of corpus callosum (disorder)
  • Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome
  • Infantile osteopetrosis with neuroaxonal dysplasia syndrome
  • corpus callosum agenesis
  • Temtamy Shalash syndrome
  • Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome
  • Corpus Callosum Dysgenesis
  • Corpus callosum anomalies
  • Callosal agenesis
  • Agenesis of corpus callosum (disorder)
  • Hypogeneses, Corpus Callosum
  • Andermann syndrome
  • Corpus Callosum Absences
  • Absence of Corpus Callosum
  • Microcephaly, polymicrogyria, corpus callosum agenesis syndrome
  • Aplasia of corpus callosum
  • Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome
  • Corpus Callosum Ageneses
  • Corpus Callosum Dysgeneses
  • Dysgenesis of corpus callosum
  • Microcephaly, thin corpus callosum, intellectual disability syndrome
  • Agenesis, Corpus Callosum
  • Congenital malformation of corpus callosum
  • Mass of preauricular region
  • Corpus Callosum, Agenesis Of
  • Hypoplasia of corpus callosum
  • Agenesis of corpus callosum with lipoma
  • Da Silva syndrome
  • Agenesis of corpus callosum and abnormal genitalia syndrome
  • Corpus Callosum Hypogenesis
  • Dysgeneses, Corpus Callosum
  • Agenesis of corpus callosum
  • Proud Levine Carpenter syndrome
  • Absence of the corpus callosum
  • Congenital hypoplasia of cerebral white matter
  • Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome
  • Dysgenesis, Corpus Callosum
  • Charlevoix disease
  • Notched iris
  • Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome
  • X-linked lissencephaly with ambiguous genitalia
  • Corpus Callosum Hypogeneses
  • Curatolo Cilio Pessagno syndrome
  • Dysplastic or absent corpus callosum
  • agenesis callosum corpus
  • Spastic quadriplegia, thin corpus callosum, progressive postnatal microcephaly syndrome
  • Acrocallosal syndrome
  • Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome
  • Congenital coloboma of iris
  • Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome
  • Corpus Callosum Absence
  • ACC - Agenesis of corpus callosum
  • 7q36.3 microduplication syndrome
  • Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome
  • Agenesis of the corpus callosum
  • L1 syndrome
  • Congenital anomaly of corpus callosum
  • X-linked lissencephaly with abnormal genitalia syndrome
  • X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome
  • Microcephaly, corpus callosum agenesis, abnormal genitalia syndrome
  • Atrophy of corpus callosum
  • Congenital absence of corpus callosum
  • Hypogenesis, Corpus Callosum
  • Hemispheric cerebral hypoplasia
  • Infantile osteopetrosis with neuroaxonal dysplasia
  • Graham Cox syndrome
  • Ageneses, Corpus Callosum
  • White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome
  • Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome
  • Absent corpus callosum
  • Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome
  • Congenital hypoplasia of cerebral hemisphere
  • X-linked complicated corpus callosum dysgenesis
  • CRASH syndrome
  • Agenesis of corpus callosum with polyneuropathy
  • Hypogenesis of corpus callosum
  • Proud syndrome
  • Partial agenesis of corpus callosum
  • Agenesis of corpus callosum with peripheral neuropathy
Frequently Asked Questions
What is the ICD-10 code for congenital malformations of corpus callosum?

The ICD-10-CM code for congenital malformations of corpus callosum is Q04.0. The full clinical description is "Congenital malformations of corpus callosum". Q04.0 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q04.0 mean?

ICD-10-CM code Q04.0 represents “Congenital malformations of corpus callosum”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q04.0 a billable code?

Yes, Q04.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q04.0 in?

Q04.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q04.0?

Q04.0 has Excludes1 notes indicating codes that cannot be used together with it, including: cyclopia (Q87.0); macrocephaly (Q75.3).

What SNOMED CT codes does Q04.0 map to?

Q04.0 maps to 31 SNOMED CT concepts: 1208720000, 5102002, 1237418002, 715951007, 763797003, and 26 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q04.0?

Q04.0 is linked to 2 UMLS Concept Unique Identifiers: C0175754, C0431366. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q04.0 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformations of corpus callosum affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q04.0?

Q04.0 maps to the ICD-11 code: LA05.3 (Corpus callosum agenesis).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.