Q43.9
BillableCongenital malformation of intestine, unspecified
Congenital malformation of intestine, unspecified
Status
Billable / Specific
Parent Code
Q43Coding Notes
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 anomaly of large intestine1492007
- Congenital anomaly of anus11194003
- Anorectal anomaly33225004
- Anorectal malformation33225004
- Congenital anomaly of small intestine55193002
- Anorectal fistula72779005
- Congenital absence of radius84918006
- Congenital anomaly of rectum86993003
- Congenital anomaly of intestinal tract126764002
- Congenital abnormality of duodenum128335001
- Congenital anomaly of duodenum128335001
- Anal atresia204712000
- Aproctia204712000
- Atresia ani204712000
- Congenital atresia of anus204712000
- Congenital imperforate anus204712000
- Imperforate anus204712000
- Telecanthus246803005
- Congenital fistula of rectum253773000
- Congenital fistula of anus253774006
- Congenital nephritis276585000
- Congenital fistula of rectum and anus302952007
- MOTA - Manitoba oculotrichoanal syndrome703539006
- Manitoba oculotrichoanal syndrome703539006
- Marles syndrome703539006
- Marles-Greenburg-Persaud syndrome703539006
- CDAGS (craniosynostosis, clavicular hypoplasia, delayed closure of fontanelle, anal anomalies, genitourinary malformations, skin eruption) syndrome720812002
- CDAGS syndrome720812002
- Craniosynostosis, anal anomaly, porokeratosis syndrome720812002
- Thymic, renal, anal, lung dysplasia syndrome723555007
- Thymic-renal-anal-lung dysplasia723555007
- STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome723581006
- STAR syndrome723581006
- Syndactyly, telecanthus, anogenital and renal malformation syndrome723581006
- Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome723676007
- Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome763066009
- Houlston Ironton Temple syndrome763066009
- Deafness, nephritis, anorectal malformation syndrome766249007
- Lowe Kohn Cohen syndrome766249007
- Absent radius, anogenital anomalies syndrome771264005
- Congenital anorectal fistula due to high anorectal malformation897594002
- High anorectal malformation with fistula897594002
- Congenital anorectal fistula due to low anorectal malformation897595001
- Low anorectal malformation with fistula897595001
- Congenital anorectal fistula due to intermediate anorectal malformation1003398002
- Intermediate anorectal malformation with fistula1003398002
- Aplasia of bone of forearm1145452004
- Aplasia of bone of radius and/or ulna1145452004
- Aplasia of radius1145466009
- Aplastic desmosis coli1222675000
- Primary desmosis coli1222675000
- Congenital non-syndromic anorectal malformation1264114007
- Non-syndromic ARM (anorectal malformation)1264114007
- Non-syndromic anorectal malformation1264114007
UMLS
- Congenital abnormality of intestineC1290601
- Congenital anomaly of intestinal tractC1290601
- Congenital anomaly of intestinal tract (disorder)C1290601
- Congenital anomaly of lower alimentary tractC1290601
- Congenital anomaly of lower alimentary tract (disorder)C1290601
- Congenital anomaly of lower gastrointestinal tractC1290601
- Congenital deformity of lower alimentary tractC1290601
- Congenital malformation of intestine, unspecifiedC1290601
Frequently Asked Questions
What is the ICD-10 code for congenital malformation of intestine, unspecified?
The ICD-10-CM code for congenital malformation of intestine, unspecified is Q43.9. The full clinical description is "Congenital malformation of intestine, unspecified". Q43.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q43.9 mean?
ICD-10-CM code Q43.9 represents "Congenital malformation of intestine, unspecified". 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 Q43.9 a billable code?
Yes, Q43.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q43.9 in?
Q43.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q43.9 map to?
Q43.9 maps to 30 SNOMED CT concepts: 771264005, 204712000, 33225004, 72779005, 1145452004, and 25 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q43.9?
Q43.9 is linked to 1 UMLS Concept Unique Identifier: C1290601. 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.