Q04.2
BillableHoloprosencephaly
Holoprosencephaly
Status
Billable / Specific
Parent Code
Q04Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- Kundrat syndrome30278004
- Kundrat's syndrome30278004
- Pseudotrisomy D>1< syndrome30278004
- Familial alobar holoprosencephaly30915001
- HPE - Holoprosencephaly30915001
- Holoprosencephaly30915001
- Holoprosencephaly sequence30915001
- Congenital absence of pancreas82949000
- Cebocephalus204052006
- Cebocephaly204052006
- Agenesis of pancreas204806003
- Cingulosynapsis253136007
- Lobar holoprosencephaly253136007
- Olfactory aplasia253136007
- Alobar holoprosencephaly253137003
- Semi-lobar holoprosencephaly253138008
- Congenital stenosis of nasal pyriform aperture702644002
- Pyriform aperture stenosis702644002
- Camero Lituania Cohen syndrome715434005
- Genoa syndrome715434005
- Holoprosencephaly craniosynostosis syndrome715434005
- Holoprosencephaly and postaxial polydactyly syndrome716091000
- Pseudotrisomy 13 syndrome716091000
- Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome716169009
- Morse Rawnsley Sargent syndrome716169009
- Agnathia, holoprosencephaly, situs inversus syndrome722283003
- Hartsfield Bixler Demyer syndrome766032007
- Hartsfield syndrome766032007
- Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome766032007
- Holoprosencephaly with caudal dysgenesis syndrome771146007
- Middle interhemispheric variant of holoprosencephaly866053004
- Syntelencephaly866053004
- Holoprosencephaly co-occurrent with congenital nasal pyriform aperture stenosis890346002
- Holoprosencephaly with apertura pyriformis890346002
- Holoprosencephaly with nasal pyriformis aperture890346002
- Aplasia of pancreas1144555008
- Pancreatic aplasia1144555008
- HPE (holoprosencephaly) minor form1197215004
- Holoprosencephaly minor form1197215004
- Holoprosencephaly-like1197215004
- Microform holoprosencephaly1197215004
- Pancreatic agenesis, holoprosencephaly syndrome1222660008
UMLS
- Familial alobar holoprosencephalyC0079541
- HPE - HoloprosencephalyC0079541
- HPE, FAMILIALC0079541
- HPECC0079541
- HoloprosencephaliesC0079541
- HoloprosencephalyC0079541
- Holoprosencephaly (HPE)C0079541
- Holoprosencephaly sequenceC0079541
- Holoprosencephaly sequence (disorder)C0079541
- Single brain ventricleC0079541
- holoprosencephalyC0079541
Frequently Asked Questions
What is the ICD-10 code for holoprosencephaly?
The ICD-10-CM code for holoprosencephaly is Q04.2. The full clinical description is "Holoprosencephaly". Q04.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q04.2 mean?
ICD-10-CM code Q04.2 represents "Holoprosencephaly". 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 Q04.2 a billable code?
Yes, Q04.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q04.2 in?
Q04.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q04.2?
Q04.2 has Excludes1 notes indicating codes that cannot be used together with it, including: cyclopia (Q87.0); macrocephaly (Q75.3).
What SNOMED CT codes does Q04.2 map to?
Q04.2 maps to 20 SNOMED CT concepts: 204806003, 722283003, 253137003, 1144555008, 715434005, and 15 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q04.2?
Q04.2 is linked to 1 UMLS Concept Unique Identifier: C0079541. 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.