Q13.1
BillableAbsence of iris
Absence of iris
Status
Billable / Specific
Parent Code
Q13Coding 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 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)
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code Q13.1?
ICD-10-CM code Q13.1 represents "Absence of iris". It 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 you should also code: code for 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.
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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.