Q43.1
BillableHirschsprung's disease
Hirschsprung's disease
Status
Billable / Specific
Parent Code
Q43Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Aganglionosis
- Congenital (aganglionic) megacolon
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
- Congenital dilatation of colon24291004
- Congenital megacolon24291004
- Central alveolar hypoventilation syndrome24825006
- Waardenburg syndrome47434006
- Waardenburg's syndrome47434006
- Secondary congenital megacolon197140007
- Secondary megacolon - congenital197140007
- Aganglionic megacolon204739008
- Aganglionosis204739008
- Congenital aganglionic megacolon204739008
- HD - Hirschsprung's disease204739008
- Hirschsprung disease204739008
- Hirschsprung's disease204739008
- Long segment Hirschsprung disease204740005
- Long segment Hirschsprung's disease204740005
- Short segment Hirschsprung disease204741009
- Short segment Hirschsprung's disease204741009
- Total intestinal aganglionosis204745000
- TCA - Total colonic aganglionosis253780003
- Total colonic aganglionosis253780003
- Aganglionosis of Auerbach plexus360434004
- Aganglionosis of Auerbach's plexus360434004
- Aganglionosis of colon360441005
- CCHS - Congenital central hypoventilation399040002
- Congenital central hypoventilation399040002
- Congenital pulmonary hypoventilation399040002
- Ondine curse399040002
- Hirschsprung disease-intellectual disability syndrome703535000
- Hirschsprung disease-mental retardation syndrome703535000
- Mowat-Wilson syndrome703535000
- Shah Waardenburg syndrome715952000
- Waardenburg Hirschsprung syndrome715952000
- Waardenburg Shah syndrome715952000
- Waardenburg syndrome co-occurrent with Hirschsprung disease715952000
- Waardenburg syndrome type 4715952000
- Goldberg Shprintzen megacolon syndrome717822006
- Megacolon microcephaly syndrome717822006
- Congenital central alveolar hypoventilation with Hirschsprung disease syndrome719972004
- Haddad syndrome719972004
- Ondine Hirschsprung disease719972004
- Ondine Hirschsprung syndrome719972004
- Hirschsprung disease with deafness and polydactyly syndrome721221000
- Santos Mateus Leal syndrome721221000
- Hirschsprung disease with type D brachydactyly syndrome721222007
- Al Gazali Donnai Muller syndrome721223002
- Hirschsprung disease with nail hypoplasia and dysmorphism721223002
- Hirschsprung disease of rectosigmoid region721608001
- Rectosigmoid Hirschsprung disease721608001
- Extensive aganglionosis Hirschsprung disease721609009
- Aganglionosis of large intestine723183004
- Neurologic Waardenburg Shah syndrome765325002
- PCWH - peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease765325002
- Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease765325002
- Hirschsprung disease, ganglioneuroblastoma syndrome783737007
- Hirschsprung disease and intellectual disability due to 2q22 microdeletion890118006
- Hirschsprung disease and intellectual disability due to del(2)(q22)890118006
- Hirschsprung disease and intellectual disability due to monosomy 2q22890118006
- Mowat-Wilson syndrome due to 2q22 microdeletion890118006
- Mowat-Wilson syndrome due to del(2)q(22)890118006
- Mowat-Wilson syndrome due to monosomy 2q22890118006
- Aganglionosis of small intestine1142282000
- Congenital aganglionosis of small intestine1142282000
- Congenital hypoplasia of nail unit1144442009
UMLS
- Aganglionic MegacolonC0019569
- Aganglionic megacolonC0019569
- AganglionosisC0019569
- CONGEN MEGACOLONC0019569
- Congenital (aganglionic) megacolonC0019569
- Congenital MegacolonC0019569
- Congenital aganglionic megacolonC0019569
- Congenital aganglionic megacolon (disorder)C0019569
- Congenital intestinal aganglionosisC0019569
- Congenital megacolonC0019569
- Disease, HirschsprungC0019569
- Disease, Hirschsprung'sC0019569
- Enlarged colon lacking nerve cellsC0019569
- HD - Hirschsprung's diseaseC0019569
- HIRSCHSPRUNG DISC0019569
- HIRSCHSPRUNGS DISC0019569
- HSCRC0019569
- Hirschsprung DiseaseC0019569
- Hirschsprung diseaseC0019569
- Hirschsprung megacolonC0019569
- Hirschsprung's DiseaseC0019569
- Hirschsprung's diseaseC0019569
- Hirschsprungs DiseaseC0019569
- MEGACOLON CONGENC0019569
- Megacolon congenitalC0019569
- Megacolon, AganglionicC0019569
- Megacolon, CongenitalC0019569
- Pelvirectal achalasiaC0019569
- aganglionic megacolonC0019569
- aganglionosisC0019569
- congenital megacolonC0019569
- disease hirschsprungC0019569
- disease hirschsprung'sC0019569
- disease hirschsprungsC0019569
- diseases hirschsprungC0019569
- hirschsprung diseaseC0019569
- hirschsprung's diseaseC0019569
- hirschsprungs diseaseC0019569
- megacolon congenitalC0019569
- pelvirectal achalasiaC0019569
Frequently Asked Questions
What is the ICD-10 code for hirschsprung's disease?
The ICD-10-CM code for hirschsprung's disease is Q43.1. The full clinical description is "Hirschsprung's disease". Q43.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q43.1 mean?
ICD-10-CM code Q43.1 represents "Hirschsprung's disease". 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 Q43.1 a billable code?
Yes, Q43.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q43.1 in?
Q43.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q43.1 map to?
Q43.1 maps to 27 SNOMED CT concepts: 204739008, 360434004, 360441005, 723183004, 1142282000, and 22 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q43.1?
Q43.1 is linked to 1 UMLS Concept Unique Identifier: C0019569. 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.