Cleft iris
Renal glycosuria
Congenital abnormality of sclera
Thin cornea
Corneal arcus
Bilateral cornea plana
Cornea small
Microcornea, posterior megalolenticonus, persistent foetal vasculature, coloboma syndrome
Prolapse of uvea
Arcus juvenilis
Congenital absence of lens
Peters plus syndrome
MGCN - Megalocornea
MPPC (microcornea, posterior megalolenticonus, persistent foetal vasculature, coloboma) syndrome
Megalocornea, spherophakia, secondary glaucoma syndrome
Chorioretinal atrophy
Microcornea
Congenital macrocornea
MMCAT syndrome
Megalophthalmos
Microcornea (disorder)
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome
Peter's anomaly
Juvenile cataract, microcornea, renal glucosuria syndrome
Macrophthalmia
Congenital anterior staphyloma
Peters anomaly
Juvenile cataract
Congenital keratoconus
Congenital cataract microcornea with corneal opacity
Microcephalus microcornea syndrome of Seemanova type
Cornea of eye less than 10mm in diameter
peters' anomaly
Microcornea with corectopia and macular hypoplasia syndrome
Macrophthalmos
Megalophthalmus
Microcornea with glaucoma and absent frontal sinus syndrome
Congenital anomaly of cornea
Irido-corneo-trabecular dysgenesis (disorder)
MRCS (microcornea, rod-cone dystrophy, cataract, posterior staphyloma) syndrome
Cataract and microcornea syndrome
MRCS syndrome
Congenital keratoglobus
Lenticonus
Cornea plana of both corneas
Anterior embryotoxon
Microcornea of bilateral eyes
Cornea globular
Microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma syndrome
Peters congenital glaucoma
Glaucoma and corneal anomaly
Enlarged cornea
Posterior embryotoxon
MPPC (microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma) syndrome
Congenital keratoconus posticus circumscriptus
Cornea enlarged
Arcus of cornea
Small cornea
Microcephaly microcornea syndrome Seemanova type
anomalies peters
Corneal size and shape anomalies
Notched iris
Seemanova Lesny syndrome
Congenital malformation of cornea NOS
Bilateral congenital anomaly of corneas
Colobomatous macrophthalmia with microcornea syndrome
Fundus coloboma
Congenital aphakia
MACOM (macrophthalmia colobomatous with microcornea) syndrome
Congenital coloboma of iris
Coloboma of fundus
Congenital structural abnormality of bilateral corneas
Keratoglobus
Scleral ectasia
Congenital structural abnormality of right cornea
Congenital arcus juvenilis
Congenital coloboma of optic disc
Microcorneas
Renal glucosuria
Embryotoxon
Corneal staphyloma
Congenital anomaly of nasal sinuses
Cornea plana
Congenital anomaly of both corneas
Congenital structural abnormality of left cornea
Congenital corneal malformation
Childhood cataract
Megalophthalmia
Cornea plana of bilateral corneas
MMCAT (microcornea, myopic chorioretinal atrophy, telecanthus) syndrome
Megalocornea
Agenesis of lens
anomaly peter
Bilateral microcornea
CCMCO - congenital cataract microcornea with corneal opacity
Haney-Falls syndrome
Irido-corneo-trabecular dysgenesis
Ectasia of sclera
Congenital megalocornea
Uveal prolapse
Infantile and/or juvenile cataract
Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome
Familial renal glucosuria
Cataract in child
Cornea flattened
Congenital structural abnormality of cornea
Peter anomaly
Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome
Congenital anomaly of bilateral corneas
Corneal thinning
Congenital optic disc coloboma
Posterior lenticonus
Congenital anomaly of sclera

Frequently Asked Questions

What is the ICD-10 code for other congenital corneal malformations?

The ICD-10-CM code for other congenital corneal malformations is Q13.4. The full clinical description is "Other congenital corneal malformations". Q13.4 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q13.4 mean?

ICD-10-CM code Q13.4 represents “Other congenital corneal malformations”. 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 Q13.4 a billable code?

Yes, Q13.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q13.4 in?

Q13.4 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q13.4 map to?

Q13.4 maps to 53 SNOMED CT concepts: 35387008, 8041000119108, 231925004, 231924000, 15987551000119107, and 48 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q13.4?

Q13.4 is linked to 4 UMLS Concept Unique Identifiers: C2910117, C0266544, C0344559, C0477983. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q13.4 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital corneal malformations 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 Q13.4?

Q13.4 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.