AutoICD API

Q13.2

Billable

Other congenital malformations of iris

Other congenital malformations of iris

Coding Notes

Related Codes(7)
ICD-11 Equivalents(1)
Also Known As / Clinical Terms(190)

SNOMED CT

Clinical Terms

  • Finding of proportion of pupil
  • Congenital anomaly of both pupils
  • Ectopia pupillae
  • Ectopic pupil
  • Pupil, Ectopic
  • Bilateral congenital hamartoma of irises
  • Familial keratoconus with cataract
  • Cornea small
  • EDICT (endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning) syndrome
  • Ectopic pupil (disorder)
  • Pupils, Ectopic
  • Congenital hamartoma of bilateral irises
  • Congenital absence of lens
  • Microcornea
  • Congenital hamartoma of left iris
  • Glaucoma of bilateral eyes due to anterior segment anomaly
  • Atretopsia
  • Congenital heterochromia iridis
  • Congenital anomaly of left pupil
  • Congenital hamartoma of right iris
  • Glaucoma of left eye due to anterior segment anomaly
  • Unequal pupil diameter
  • Congenital abnormality of iris
  • Congenital anomaly of iris
  • Bilateral congenital anomaly of pupil
  • Finding of iris pigmentation
  • Finding of pupil shape
  • Heterochromic iris
  • Embryonic cyst of iris
  • Ectopic Pupils
  • Anisocoria - unequal pupil diameter
  • Microcornea with corectopia and macular hypoplasia syndrome
  • Observation of pupil shape
  • Autosomal dominant spastic ataxia type 7
  • Miotic pupil
  • EDICT syndrome
  • Teardrop pupil
  • Deformed pupil
  • Pupil constriction
  • Heterochromia iridis
  • Atresia of pupil (disorder)
  • Iris pigmentation - finding
  • Glaucoma due to iris anomaly
  • Congenital cyst of iris
  • Glaucoma of right eye due to anterior segment anomaly
  • Glaucoma of left eye due to congenital anomaly of iris
  • Spastic ataxia with congenital miosis
  • Abnormal shape of pupil
  • Congenital anomaly of pupil
  • Glaucoma of right eye due to congenital anomaly of iris
  • Congenital hamartoma of iris of left eye
  • Holes in iris
  • Hypoplasia of iris
  • Congenital hypoplasia of iris dilator muscle
  • Glaucoma of bilateral eyes due to congenital anomaly of iris
  • Miosis
  • Corectopia
  • Congenital anomaly of right pupil
  • Atresia of pupil
  • Dyscoria
  • Anisocoria, congenital
  • Congenital aphakia
  • Anisocoria
  • Polycoria
  • Small pupil
  • Congenital hypoplasia of dilator pupillae muscle
  • McPherson Hall syndrome
  • Congenital hamartoma of iris
  • Displaced pupils
  • Congenital anisocoria
  • Congenital anisocoria (disorder)
  • Atresia iridis
  • Congenital hamartoma of iris of right eye
  • Congenital malformation of iris NOS
  • Glaucoma of both eyes due to anterior segment anomaly
  • Multiple pupil
  • Congenital hamartoma of both irises
  • Agenesis of lens
  • Congenital miosis
  • Endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning syndrome
  • Unequal pupils
  • Congenital ectopic pupil
  • Constricted pupil
  • Pseudo-polycoria
  • Ptosis, strabismus, ectopic pupil syndrome
  • Tadpole pupil
  • Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome
  • Autosomal dominant keratoconus with early-onset anterior polar cataract
  • Congenital anomaly of bilateral pupils
  • Observation of proportion of pupil
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of iris?

The ICD-10-CM code for other congenital malformations of iris is Q13.2. The full clinical description is "Other congenital malformations of iris". Q13.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q13.2 mean?

ICD-10-CM code Q13.2 represents “Other congenital malformations 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 Q13.2 a billable code?

Yes, Q13.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q13.2 in?

Q13.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q13.2 map to?

Q13.2 maps to 43 SNOMED CT concepts: 79017007, 35387008, 13045009, 17480001, 722439009, and 38 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q13.2?

Q13.2 is linked to 5 UMLS Concept Unique Identifiers: C0266549, C0266550, C2910116, C0271135, C0477982. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q13.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations 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 Q13.2?

Q13.2 maps to the ICD-11 code: LA11.Z (Structural developmental anomalies of the anterior segment of eye, unspecified).

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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.