Q13.81
BillableRieger anomaly
Rieger anomaly
Status
Billable / Specific
Parent Code
Q13.8Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Axenfeld-Rieger syndrome
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
- cleft lip and cleft palate (Q35-Q37)
- congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)
- congenital malformation of larynx (Q31.-)
- congenital malformation of lip NEC (Q38.0)
- congenital malformation of nose (Q30.-)
- congenital malformation of parathyroid gland (Q89.2)
- congenital malformation of thyroid gland (Q89.2)
Code Also
A second code may be required; sequencing depends on circumstances
- any other associated congenital malformations such as cardiac defects
Also Known As / Clinical Terms
SNOMED CT
- Rieger anomaly47507006
- Rieger syndrome47507006
- Rieger's syndrome47507006
- Acquired partial lipodystrophy75659004
- Barraquer syndrome75659004
- Barraquer-Simons disease75659004
- Barraquer-Simons syndrome75659004
- Hollander-Simons syndrome75659004
- Lipodystrophic diabetes with partial lipoatrophy75659004
- Macrodystrophia lipomatosa progressiva75659004
- Partial lipoatrophy75659004
- Progressive lipodystrophy75659004
- Progressive partial lipodystrophy75659004
- Irido-trabecular dysgenesis204154009
- Mesodermal dysgenesis of iris204154009
- Lipodystrophy, partial, with Rieger anomaly, short stature, and insulinopenic diabetes mellitus237608006
- Axenfeld syndrome417604002
- Axenfeld-Rieger syndrome417604002
UMLS
- Rieger anomalyC0265341
- Rieger SyndromeC0265341
- Rieger syndromeC0265341
- Rieger syndrome (disorder)C0265341
- Rieger's anomalyC0265341
- Rieger's syndromeC0265341
- axenfeld syndromeC0265341
- axenfeld's syndromeC0265341
- axenfelds syndromeC0265341
- rieger anomalyC0265341
- rieger syndromeC0265341
- rieger's syndromeC0265341
- riegers syndromeC0265341
- ARSC3495488
- AXRSC3495488
- Axenfeld syndromeC3495488
- Axenfeld-Rieger syndromeC3495488
- Axenfeld-Rieger syndrome (disorder)C3495488
- Iridogoniodysgenesis with somatic anomaliesC3495488
Frequently Asked Questions
What is the ICD-10 code for rieger anomaly?
The ICD-10-CM code for rieger anomaly is Q13.81. The full clinical description is "Rieger anomaly". Q13.81 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q13.81 mean?
ICD-10-CM code Q13.81 represents "Rieger anomaly". 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 Q13.81 a billable code?
Yes, Q13.81 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q13.81 in?
Q13.81 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
Are additional codes required with Q13.81?
Yes, when using Q13.81 you should also code: code for associated glaucoma (H42).
What SNOMED CT codes does Q13.81 map to?
Q13.81 maps to 5 SNOMED CT concepts: 75659004, 417604002, 204154009, 237608006, 47507006. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q13.81?
Q13.81 is linked to 2 UMLS Concept Unique Identifiers: C0265341, C3495488. 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.