2020 ICD-10-CM Diagnosis Code Q04.0

Congenital malformations of corpus callosum

    2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
  • Q04.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2020 edition of ICD-10-CM Q04.0 became effective on October 1, 2019.
  • This is the American ICD-10-CM version of Q04.0 - other international versions of ICD-10 Q04.0 may differ.
Applicable To
  • Agenesis of corpus callosum
The following code(s) above Q04.0 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to Q04.0:
  • Q00-Q99
    2020 ICD-10-CM Range Q00-Q99

    Congenital malformations, deformations and chromosomal abnormalities

    Note
    • Codes from this chapter are not for use on maternal records
    Type 2 Excludes
    • inborn errors of metabolism (E70-E88)
    Congenital malformations, deformations and chromosomal abnormalities
  • Q04
    ICD-10-CM Diagnosis Code Q04

    Other congenital malformations of brain

      2016 2017 2018 2019 2020 Non-Billable/Non-Specific Code
    Type 1 Excludes
    Other congenital malformations of brain
Approximate Synonyms
  • Absent corpus callosum
  • Agenesis of corpus callosum
  • Congenital malformation of corpus callosum
  • Corpus callosum anomaly, congenital
Clinical Information
  • A congenital abnormality characterized by the complete absence of the corpus callosum. It may be an isolated abnormality or associated with other central nervous system abnormalities or syndromes. Clinical manifestations vary. In cases of isolated corpus callosum agenesis, symptoms may be absent or minimal. In cases that are associated with other central nervous system abnormalities or syndromes, symptoms include developmental delays, motor coordination difficulties, and vision impairment.
  • Birth defect that results in a partial or complete absence of the corpus callosum. It may be isolated or a part of a syndrome (e.g., aicardi's syndrome; acrocallosal syndrome; andermann syndrome; and holoprosencephaly). Clinical manifestations include neuromotor skill impairment and intellectual disability of variable severity.
Present On Admission
POA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
  • Q04.0 is considered exempt from POA reporting.
ICD-10-CM Q04.0 is grouped within Diagnostic Related Group(s) (MS-DRG v37.0):
  • 091 Other disorders of nervous system with mcc
  • 092 Other disorders of nervous system with cc
  • 093 Other disorders of nervous system without cc/mcc
  • 791 Prematurity with major problems
  • 793 Full term neonate with major problems

Convert Q04.0 to ICD-9-CM

Code History
  • 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
  • 2017 (effective 10/1/2016): No change
  • 2018 (effective 10/1/2017): No change
  • 2019 (effective 10/1/2018): No change
  • 2020 (effective 10/1/2019): No change
Code annotations containing back-references to Q04.0:
  • Type 1 Excludes: Q04.3
    ICD-10-CM Diagnosis Code Q04.3

    Other reduction deformities of brain

      2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
    Applicable To
    • Absence of part of brain
    • Agenesis of part of brain
    • Agyria
    • Aplasia of part of brain
    • Hydranencephaly
    • Hypoplasia of part of brain
    • Lissencephaly
    • Microgyria
    • Pachygyria
    Type 1 Excludes
    • congenital malformations of corpus callosum (Q04.0)

Diagnosis Index entries containing back-references to Q04.0:

ICD-10-CM Codes Adjacent To Q04.0
Q01.2 Occipital encephalocele
Q01.8 Encephalocele of other sites
Q01.9 Encephalocele, unspecified
Q02 Microcephaly
Q03 Congenital hydrocephalus
Q03.0 Malformations of aqueduct of Sylvius
Q03.1 Atresia of foramina of Magendie and Luschka
Q03.8 Other congenital hydrocephalus
Q03.9 Congenital hydrocephalus, unspecified
Q04 Other congenital malformations of brain
Q04.0 Congenital malformations of corpus callosum
Q04.1 Arhinencephaly
Q04.2 Holoprosencephaly
Q04.3 Other reduction deformities of brain
Q04.4 Septo-optic dysplasia of brain
Q04.5 Megalencephaly
Q04.6 Congenital cerebral cysts
Q04.8 Other specified congenital malformations of brain
Q04.9 Congenital malformation of brain, unspecified
Q05 Spina bifida
Q05.0 Cervical spina bifida with hydrocephalus

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.