Q13.89
BillableOther congenital malformations of anterior segment of eye
Other congenital malformations of anterior segment of eye
Status
Billable / Specific
Parent Code
Q13.8Coding Notes
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
- Congenital anomaly of macula4041005
- Congenital abnormality of sclera32809005
- Congenital anomaly of sclera32809005
- Congenital melanosis of sclera51174006
- PPM - persistent pupillary membranes95500008
- Persistent pupillary membrane95500008
- Persistent pupillary membranes95500008
- Glaucoma due to congenital chamber angle anomaly193552006
- Glaucoma due to congenital malformation of angle of anterior chamber of eye193552006
- Congenital anomaly of angle of anterior chamber of eye251729009
- Congenital malformation of angle251729009
- Congenital malformation of angle of anterior chamber of eye251729009
- Goniodysgenesis251730004
- Barkan membrane251731000
- Trabecular dysgenesis253240006
- Axenfeld syndrome417604002
- Axenfeld-Rieger syndrome417604002
- Melanin pigmentation of eye421735009
- Congenital hypoplasia of fovea429449002
- Congenital hypoplasia of fovea centralis429449002
- GMS syndrome716024001
- Goniodysgenesis with intellectual disability and short stature syndrome716024001
- Goniodysgenesis with mental deficiency and short stature716024001
- FHONDA (foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis) syndrome782754006
- FHONDA syndrome782754006
- Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome782754006
- Congenital hypoplasia of retina1144397003
- Congenital retinal hypoplasia1144397003
- Congenital hypoplasia of macula lutea1144408000
- Congenital macular hypoplasia1144408000
- Autosomal recessive anterior segment dysgenesis1197358003
- Autosomal recessive dysgenesis of anterior segment of eye1197358003
- Angle closure due to anterior chamber angle anomaly1286831008
- Angle closure due to congenital malformation of angle of anterior chamber of eye1286831008
- Acute angle closure due to anterior chamber angle anomaly1286832001
- Acute angle closure due to congenital malformation of angle of anterior chamber of eye1286832001
- Acute angle closure of bilateral eyes1297004004
- Acute angle closure of both eyes1297004004
- Bilateral acute angle closure1297004004
- Acute angle closure of right eye due to congenital malformation of angle of anterior chamber of right eye1297259009
- Acute angle closure of left eye due to congenital malformation of angle of anterior chamber of left eye1297260004
- Acute angle closure of bilateral eyes due to congenital malformation of angle of anterior chamber of bilateral eyes1297261000
- Bilateral secondary acute angle closure1297305009
- Secondary acute angle closure of bilateral eyes1297305009
- Secondary acute angle closure of both eyes1297305009
- Angle closure of right eye due to congenital malformation of angle of anterior chamber of right eye1297339008
- Angle closure of left eye due to congenital malformation of angle of anterior chamber of left eye1297340005
- Angle closure of bilateral eyes due to congenital malformation of angle of anterior chamber of bilateral eyes1297341009
- Angle closure of both eyes due to congenital malformation of angle of anterior chamber of both eyes1297341009
- Bilateral angle closure due to congenital malformation of angle of anterior chamber of bilateral eyes1297341009
- Bilateral secondary angle closure glaucoma1306333003
- Secondary angle closure glaucoma of bilateral eyes1306333003
- Secondary angle closure glaucoma of both eyes1306333003
- Glaucoma of right eye due to congenital chamber angle anomaly1306782000
- Glaucoma of right eye due to congenital malformation of angle of anterior chamber of eye1306782000
- Congenital anomaly of angle of anterior chamber of right eye1306783005
- Congenital malformation of angle of anterior chamber of right eye1306783005
- Congenital anomaly of angle of anterior chamber of left eye1306784004
- Congenital malformation of angle of anterior chamber of left eye1306784004
- Congenital anomaly of angle of anterior chamber of bilateral eyes1306785003
- Congenital malformation of angle of anterior chamber of bilateral eyes1306785003
- Glaucoma of left eye due to congenital chamber angle anomaly1306787006
- Glaucoma of left eye due to congenital malformation of angle of anterior chamber of eye1306787006
- Bilateral glaucoma due to congenital chamber angle anomaly1306789009
- Glaucoma of bilateral eyes due to congenital malformation of angle of anterior chamber of eyes1306789009
- Glaucoma of bilateral eyes due to anterior segment anomaly15739081000119101
- Glaucoma of both eyes due to anterior segment anomaly15739081000119101
- Glaucoma of left eye due to anterior segment anomaly15739161000119109
- Glaucoma of right eye due to anterior segment anomaly15739121000119104
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of anterior segment of eye?
The ICD-10-CM code for other congenital malformations of anterior segment of eye is Q13.89. The full clinical description is "Other congenital malformations of anterior segment of eye". Q13.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q13.89 mean?
ICD-10-CM code Q13.89 represents "Other congenital malformations of anterior segment of eye". 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 Q13.89 a billable code?
Yes, Q13.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q13.89 in?
Q13.89 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q13.89 map to?
Q13.89 maps to 37 SNOMED CT concepts: 1286832001, 1297004004, 1297261000, 1297260004, 1297259009, and 32 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q13.89?
Q13.89 is linked to 1 UMLS Concept Unique Identifier: C0477984. 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.