Q13.1
BillableAbsence of iris
Absence of iris
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Aniridia
Excludes 2
Conditions not included here, but the patient may have both
- •inborn errors of metabolismE70-E88
- •cleft lip and cleft palateQ35-Q37
- •congenital malformation of cervical spine, , ,Q05.0, Q05.5, Q67.5, Q76.0-Q76.4
- •congenital malformation of larynxQ31
- •congenital malformation of lip NECQ38.0
- •congenital malformation of noseQ30
- •congenital malformation of parathyroid glandQ89.2
- •congenital malformation of thyroid glandQ89.2
Related Codes(7)
Q13.0Coloboma of iris
Q13.2Other congenital malformations of iris
Q13.3Congenital corneal opacity
Q13.4Other congenital corneal malformations
Q13.5Blue sclera
Q13.8Other congenital malformations of anterior segment of eye
Q13.9Congenital malformation of anterior segment of eye, unsp
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(82)
SNOMED CT
- 11p partial monosomy syndrome4135001
- Agenesis of iris69278003
- Aniridia69278003
- Aplasia of iris69278003
- Congenital absence of iris69278003
- Congenital aniridia69278003
- Irideraemia69278003
- Irideremia69278003
- Congenital absence of the kidney204942005
- Renal agenesis204942005
- AN1253231007
- Aniridia type 1253231007
- AN2253232000
- Aniridia type 2253232000
- Chromosome 11p13 deletion syndrome715215007
- WAGR (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome715215007
- WAGR (Wilms tumour, aniridia, genitourinary anomalies and mental retardation) syndrome715215007
- WAGR syndrome715215007
- Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome715215007
- Wilms tumour, aniridia, genitourinary anomalies and mental retardation syndrome715215007
- Aniridia and absent patella syndrome720467005
- Aniridia and intellectual disability syndrome720468000
- Aniridia, ptosis, intellectual disability, familial obesity syndrome720987001
- Deletion of part of chromosome 11726381002
- Aniridia, renal agenesis, psychomotor retardation syndrome733116005
- Sommer Rathbun Battles syndrome733116005
- Congenital anomaly of patella890399008
- Bilateral congenital aniridia of eyes15987031000119108
- Congenital aniridia of bilateral eyes15987031000119108
- Congenital aniridia of both eyes15987031000119108
- Congenital aniridia of left eye15986991000119108
- Congenital aniridia of right eye15986951000119103
UMLS
- ANIRIDIAC0003076
- Absence of irisC0003076
- Absent IrisC0003076
- Absent irisC0003076
- Agenesis of irisC0003076
- AniridiaC0003076
- Aplasia of irisC0003076
- Congenital AniridiaC0003076
- Congenital absence of irisC0003076
- Congenital aniridiaC0003076
- Congenital aniridia (disorder)C0003076
- IrideraemiaC0003076
- IrideremiaC0003076
- aniridaC0003076
- aniridiaC0003076
Clinical Terms
- Absent iris
- Irideremia
- Congenital aniridia of left eye
- WAGR (Wilms tumour, aniridia, genitourinary anomalies and mental retardation) syndrome
- Congenital Aniridia
- 11p partial monosomy syndrome
- Congenital aniridia of right eye
- Agenesis of iris
- AN1
- Congenital absence of the kidney
- Congenital aniridia (disorder)
- Congenital aniridia of both eyes
- Deletion of part of chromosome 11
- Renal agenesis
- Aniridia type 2
- Congenital aniridia of bilateral eyes
- Congenital anomaly of patella
- ANIRIDIA
- Wilms tumour, aniridia, genitourinary anomalies and mental retardation syndrome
- AN2
- Chromosome 11p13 deletion syndrome
- Aniridia and intellectual disability syndrome
- Aniridia, renal agenesis, psychomotor retardation syndrome
- WAGR (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome
- Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
- Aniridia and absent patella syndrome
- Bilateral congenital aniridia of eyes
- WAGR syndrome
- Aniridia, ptosis, intellectual disability, familial obesity syndrome
- Aplasia of iris
- Sommer Rathbun Battles syndrome
- Aniridia type 1
- Congenital absence of iris
- Irideraemia
- anirida
Frequently Asked Questions
What is the ICD-10 code for absence of iris?
The ICD-10-CM code for absence of iris is Q13.1. The full clinical description is "Absence of iris". Q13.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q13.1 mean?
ICD-10-CM code Q13.1 represents “Absence of iris”. 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 Q13.1 a billable code?
Yes, Q13.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q13.1 in?
Q13.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
Are additional codes required with Q13.1?
Yes, when using Q13.1, also report: associated glaucoma (H42).
What SNOMED CT codes does Q13.1 map to?
Q13.1 maps to 15 SNOMED CT concepts: 4135001, 253231007, 253232000, 69278003, 720467005, and 10 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q13.1?
Q13.1 is linked to 1 UMLS Concept Unique Identifier: C0003076. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q13.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like absence of iris 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 Q13.1?
Q13.1 maps to the ICD-11 code: LA11.3 (Aniridia).
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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.