Q04.0
BillableCongenital malformations of corpus callosum
Congenital malformations of corpus callosum
Status
Billable / Specific
Parent Code
Q04Coding 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
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- ACC - Agenesis of corpus callosum5102002
- Absent corpus callosum5102002
- Agenesis of corpus callosum5102002
- Congenital absence of corpus callosum5102002
- Cleft iris51485001
- Congenital coloboma of iris51485001
- Notched iris51485001
- Congenital anomaly of corpus callosum204042007
- Congenital malformation of corpus callosum204042007
- Dysgenesis of corpus callosum204042007
- Hypoplasia of corpus callosum204043002
- Aplasia of corpus callosum204044008
- Agenesis of corpus callosum with lipoma253139000
- Partial agenesis of corpus callosum253140003
- Atrophy of corpus callosum253142006
- Disorder of serine metabolism303097007
- Mass of preauricular region447868007
- Agenesis of corpus callosum with peripheral neuropathy702439002
- Agenesis of corpus callosum with polyneuropathy702439002
- Andermann syndrome702439002
- Charlevoix disease702439002
- Acrocallosal syndrome715951007
- CRASH syndrome716996008
- Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome716996008
- Hypoplasia of corpus callosum, intellectual disability, adducted thumbs, spasticity, hydrocephalus syndrome716996008
- L1 syndrome716996008
- X-linked lissencephaly with abnormal genitalia syndrome717632002
- X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome717632002
- X-linked lissencephaly with ambiguous genitalia717632002
- Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome719947004
- Temtamy Shalash syndrome719947004
- Temtamy syndrome719947004
- Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome722282008
- Graham Cox syndrome722282008
- Da Silva syndrome722455002
- Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome722455002
- Infantile osteopetrosis with neuroaxonal dysplasia724226009
- Infantile osteopetrosis with neuroaxonal dysplasia syndrome724226009
- Agenesis of corpus callosum and abnormal genitalia syndrome763797003
- Corpus callosum agenesis, abnormal genitalia syndrome763797003
- Microcephaly, corpus callosum agenesis, abnormal genitalia syndrome763797003
- Proud Levine Carpenter syndrome763797003
- Proud syndrome763797003
- Microcephaly, thin corpus callosum, intellectual disability syndrome770721009
- Microcephaly, polymicrogyria, corpus callosum agenesis syndrome773305003
- Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome773497001
- Curatolo Cilio Pessagno syndrome783703004
- White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome783703004
- X-linked complicated corpus callosum dysgenesis1010630006
- Congenital hypoplasia of cerebral hemisphere1144337000
- Hemispheric cerebral hypoplasia1144337000
- Congenital hypoplasia of cerebral white matter1144343003
- Microcephaly, corpus callosum and cerebellar vermis hypoplasia, facial dysmorphism, intellectual disability syndrome1167375003
- 7q36.3 microduplication syndrome1208720000
- Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome1208720000
- Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome1208727002
- ASCT1 deficiency1237418002
- Spastic quadriplegia, thin corpus callosum, progressive postnatal microcephaly syndrome1237418002
- Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome1237418002
- Microcephaly, corpus callosum hypoplasia, intellectual disability, facial dysmorphism syndrome1254650002
UMLS
- ACCC0175754
- ACC - Agenesis of corpus callosumC0175754
- Absence of Corpus CallosumC0175754
- Absence of corpus callosumC0175754
- Absence of the corpus callosumC0175754
- Absent corpus callosumC0175754
- Ageneses, Corpus CallosumC0175754
- Agenesis corpus callosumC0175754
- Agenesis of Corpus CallosumC0175754
- Agenesis of corpus callosumC0175754
- Agenesis of corpus callosum (disorder)C0175754
- Agenesis of the corpus callosumC0175754
- Agenesis, Corpus CallosumC0175754
- CORPUS CALLOSUM, AGENESIS OFC0175754
- Callosal agenesisC0175754
- Congenital absence of corpus callosumC0175754
- Corpus Callosum AbsenceC0175754
- Corpus Callosum AbsencesC0175754
- Corpus Callosum AgenesesC0175754
- Corpus Callosum AgenesisC0175754
- Corpus Callosum DysgenesesC0175754
- Corpus Callosum DysgenesisC0175754
- Corpus Callosum HypogenesesC0175754
- Corpus Callosum HypogenesisC0175754
- Corpus Callosum, Agenesis OfC0175754
- Corpus callosum agenesisC0175754
- Corpus callosum hypogenesisC0175754
- Corpus callosum, agenesis ofC0175754
- Dysgeneses, Corpus CallosumC0175754
- Dysgenesis, Corpus CallosumC0175754
- Dysplastic or absent corpus callosumC0175754
- Hypogeneses, Corpus CallosumC0175754
- Hypogenesis of corpus callosumC0175754
- Hypogenesis, Corpus CallosumC0175754
- agenesis callosum corpusC0175754
- agenesis corpus callosumC0175754
- agenesis of corpus callosumC0175754
- corpus callosum agenesisC0175754
- Congenital anomaly of corpus callosumC0431366
- Congenital malformation of corpus callosumC0431366
- Congenital malformation of corpus callosum (disorder)C0431366
- Congenital malformations of corpus callosumC0431366
- Corpus callosum anomaliesC0431366
- Dysgenesis of corpus callosumC0431366
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.
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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.