AutoICD API

Q13.81

Billable

Rieger anomaly

Rieger anomaly

Status

Billable / Specific

Parent Code

Q13.8

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Axenfeld-Rieger syndrome

Excludes 2

Conditions not included here, but the patient may have both

Use Additional Code

Additional codes that should follow this code

Code Also

A second code may be required; sequencing depends on circumstances

  • any other associated congenital malformations such as cardiac defects
Related Codes(1)
Q13.89

Other congenital malformations of anterior segment of eye

Billable
Also Known As / Clinical Terms(63)

SNOMED CT

UMLS

Clinical Terms

  • Acquired partial lipodystrophy
  • Irido-trabecular dysgenesis
  • Axenfeld syndrome
  • axenfelds syndrome
  • rieger's syndrome
  • Iridogoniodysgenesis with somatic anomalies
  • Macrodystrophia lipomatosa progressiva
  • riegers syndrome
  • Lipodystrophic diabetes with partial lipoatrophy
  • Partial lipoatrophy
  • rieger syndrome
  • AXRS
  • axenfeld's syndrome
  • Rieger's anomaly
  • Axenfeld-Rieger syndrome
  • Hollander-Simons syndrome
  • Rieger syndrome (disorder)
  • Mesodermal dysgenesis of iris
  • Barraquer-Simons disease
  • Barraquer syndrome
  • Progressive lipodystrophy
  • ARS
  • Barraquer-Simons syndrome
  • Axenfeld-Rieger syndrome (disorder)
  • Lipodystrophy, partial, with Rieger anomaly, short stature, and insulinopenic diabetes mellitus
  • Progressive partial lipodystrophy
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, also report: 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: C3495488, C0265341. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q13.81 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like rieger anomaly affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q13.81?

There is no direct ICD-11 mapping available for Q13.81 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.