Q44.71
BillableAlagille syndrome
Alagille syndrome
Status
Billable / Specific
Parent Code
Q44.7Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Alagille-Watson syndrome
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Code Also
A second code may be required; sequencing depends on circumstances
- , if applicable, associated malformations affecting other systems
Also Known As / Clinical Terms
SNOMED CT
UMLS
- ALGSC0085280
- AHDC0085280
- ALAGILLE SYNDROMEC0085280
- ALAGILLE-WATSON SYNDROMEC0085280
- ARTERIOHEPATIC DYSPLASIAC0085280
- AWSC0085280
- Alagille SyndromeC0085280
- Alagille Watson SyndromeC0085280
- Alagille syndromeC0085280
- Alagille's SyndromeC0085280
- Alagille's syndromeC0085280
- Alagille-Watson SyndromeC0085280
- Alagille-Watson syndromeC0085280
- Alagilles SyndromeC0085280
- Arteriohepatic DysplasiaC0085280
- Arteriohepatic Dysplasia (AHD)C0085280
- Arteriohepatic dysplasiaC0085280
- Arteriohepatic dysplasia (AHD)C0085280
- Arteriohepatic dysplasia (disorder)C0085280
- CHOLESTASIS WITH PERIPHERAL PULM STENOSISC0085280
- CHOLESTASIS WITH PERIPHERAL PULMONARY STENOSISC0085280
- Cardiovertebral SyndromeC0085280
- Cardiovertebral syndromeC0085280
- Cholestasis with Peripheral Pulmonary StenosisC0085280
- Cholestasis with peripheral pulmonary stenosisC0085280
- Dysplasia, ArteriohepaticC0085280
- Dysplasia, Arteriohepatic (AHD)C0085280
- HEPATIC DUCTULAR HYPOPLASIA, SYNDROMATICC0085280
- Hepatic Ductular Hypoplasia, SyndromaticC0085280
- Hepatic ductular hypoplasiaC0085280
- Hepatofacioneurocardiovertebral SyndromeC0085280
- Hepatofacioneurocardiovertebral syndromeC0085280
- Syndrome, AlagilleC0085280
- Syndrome, Alagille WatsonC0085280
- Syndrome, Alagille'sC0085280
- Syndrome, Alagille-WatsonC0085280
- Syndrome, CardiovertebralC0085280
- Syndrome, HepatofacioneurocardiovertebralC0085280
- Syndrome, Watson AlagilleC0085280
- Syndrome, Watson MillerC0085280
- Watson Alagille SyndromeC0085280
- Watson Miller SyndromeC0085280
- Watson-Alagille syndromeC0085280
- Watson-Miller syndromeC0085280
- alagille syndromeC0085280
- alagille-watson syndromeC0085280
- alagilles syndromeC0085280
- arteriohepatic dysplasiaC0085280
- syndrome alagilleC0085280
- syndrome, Watson-MillerC0085280
Frequently Asked Questions
What is the ICD-10 code for alagille syndrome?
The ICD-10-CM code for alagille syndrome is Q44.71. The full clinical description is "Alagille syndrome". Q44.71 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q44.71 mean?
ICD-10-CM code Q44.71 represents "Alagille syndrome". 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 Q44.71 a billable code?
Yes, Q44.71 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q44.71 in?
Q44.71 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q44.71 map to?
Q44.71 maps to 2 SNOMED CT concepts: 31742004, 308861002. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q44.71?
Q44.71 is linked to 1 UMLS Concept Unique Identifier: C0085280. 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.