Category · FY2027
Q13 Congenital malformations of anterior segment of eye
- Header · not billable
Q13 is not billable. The category heads 9 billable codes in FY2027, grouped under 8 subdivisions.
Index → code
Where it sits
- Chapter 17 Congenital malformations, deformations, chromosomal abnormalities, and genetic disorders (Q00-QA1)
- Q10-Q18 Congenital malformations of eye, ear, face and neck (Q10-Q18)
- Q13 Congenital malformations of anterior segment of eye
- Billable codes
- 9
- Subdivisions
- 8
- CC / MCC codes
- 0 / 0
- HCC V28 codes
- 0
- New FY2027
- 0
- Index entries
- 51
Codes in Q13
- Q13.0Coloboma of irisBillableExempt
Inclusion terms 1
Inclusion terms
- Coloboma NOS
- Q13.1Absence of irisBillableExempt
Inclusion terms 1, Use additional code 1
Inclusion terms
- Aniridia
Use additional code
- code for associated glaucoma (H42) H42
- Q13.2Other congenital malformations of irisBillableExempt
Inclusion terms 4
Inclusion terms
- Anisocoria, congenital
- Atresia of pupil
- Congenital malformation of iris NOS
- Corectopia
- Q13.3Congenital corneal opacityBillableExempt
- Q13.4Other congenital corneal malformationsBillableExempt
Inclusion terms 3
Inclusion terms
- Congenital malformation of cornea NOS
- Microcornea
- Peter's anomaly
- Q13.5Blue scleraBillableExempt
- Q13.8Other congenital malformations of anterior segment of eyeHeader
- Q13.81Rieger anomalyBillableExempt
Inclusion terms 1, Use additional code 1, Code also 1
Inclusion terms
- Axenfeld-Rieger syndrome
Use additional code
- code for associated glaucoma (H42) H42
Code also
- any other associated congenital malformations such as cardiac defects
- Q13.89Other congenital malformations of anterior segment of eyeBillableExempt
- Q13.9Congenital malformation of anterior segment of eye, unspecifiedBillableExempt
Instructions
Notes that also apply
Block Q10-Q18 instructions (Excludes2 7): printed on the block page.
Chapter 17 instructions (Notes 1, Excludes2 1): printed on the chapter 17 page.
Index entries
- Coloboma (iris) → Q13.0
- Aniridia (congenital) → Q13.1
- Irideremia → Q13.1
- Corectopia → Q13.2
- Heterochromia (congenital) → Q13.2
- Notch of iris → Q13.2
- Polycoria → Q13.2
- Embryotoxon → Q13.4
- Keratomegaly → Q13.4
- Microcornea (congenital) → Q13.4
- Peter's anomaly → Q13.4
- Rieger anomaly or syndrome → Q13.81
- Mesostromal dysgenesia → Q13.89
- Pupillary membrane (persistent) → Q13.89
- Absence (of) (organ or part) (complete or partial)›iris, congenital → Q13.1
- Agenesis›iris (dilator fibers) → Q13.1
- Aplasia›iris → Q13.1
- Anisocoria (pupil)›congenital → Q13.2
- Anomaly, anomalous (congenital) (unspecified type)›iris → Q13.2
- Anomaly, anomalous (congenital) (unspecified type)›opticociliary vessels → Q13.2
- Anomaly, anomalous (congenital) (unspecified type)›pupil → Q13.2
- Atresia, atretic›pupil → Q13.2
- Deformity›opticociliary vessels (congenital) → Q13.2
- Deformity›pupil (congenital) → Q13.2
- Malformation (congenital)›iris → Q13.2
- Anomaly, anomalous (congenital) (unspecified type)›cornea (shape) → Q13.4
- Anomaly, anomalous (congenital) (unspecified type)›Peter's → Q13.4
- Axenfeld's›degeneration (calcareous) → Q13.4
- Cornea›plana → Q13.4
- Keratectasia›congenital → Q13.4
- Keratoconus›congenital → Q13.4
- Malformation (congenital)›cornea → Q13.4
- Blue›sclera → Q13.5
- Anomaly, anomalous (congenital) (unspecified type)›Rieger → Q13.81
- Syndrome›Axenfeld-Rieger → Q13.81
- Defect, defective›Descemet's membrane, congenital → Q13.89
- Membrana›capsularis lentis posterior → Q13.89
- Persistence, persistent (congenital)›pupillary membrane → Q13.89
- Glaucoma›in (due to)›aniridia → Q13.1 [H42]
- Deformity›iris (acquired)›congenital → Q13.2
11 more, longer entries are not listed; the search box finds them by word.
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