Q13.4
BillableOther congenital corneal malformations
Other congenital corneal malformations
Status
Billable / Specific
Parent Code
Q13Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital malformation of cornea NOS
- Microcornea
- Peter's anomaly
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
- Cornea small26098002
- Microcornea26098002
- Congenital abnormality of sclera32809005
- Congenital anomaly of sclera32809005
- Agenesis of lens35387008
- Congenital absence of lens35387008
- Congenital aphakia35387008
- Coloboma of fundus39302008
- Fundus coloboma39302008
- Congenital coloboma of optic disc44295002
- Congenital optic disc coloboma44295002
- Cleft iris51485001
- Congenital coloboma of iris51485001
- Notched iris51485001
- Corneal staphyloma52476003
- Congenital keratoconus63216003
- Congenital keratoconus posticus circumscriptus75340008
- Haney-Falls syndrome75340008
- Macrophthalmia93181004
- Macrophthalmos93181004
- Megalophthalmia93181004
- Megalophthalmos93181004
- Megalophthalmus93181004
- Posterior lenticonus95482000
- Chorioretinal atrophy95686007
- Congenital anomaly of nasal sinuses128275006
- Congenital anomaly of cornea128352002
- Congenital corneal malformation128352002
- Congenital structural abnormality of cornea128352002
- Congenital keratoglobus204118005
- Corneal size and shape anomalies204143004
- Cornea flattened204145006
- Cornea plana204145006
- Irido-corneo-trabecular dysgenesis204153003
- Peter's anomaly204153003
- Peters anomaly204153003
- Familial renal glucosuria226309007
- Arcus of cornea231924000
- Corneal arcus231924000
- Arcus juvenilis231925004
- Glaucoma and corneal anomaly232083008
- Lenticonus253221000
- Embryotoxon253228006
- Congenital anterior staphyloma253230008
- Renal glucosuria267430007
- Renal glycosuria267430007
- Congenital macrocornea268158009
- Congenital megalocornea268158009
- Cornea enlarged268158009
- Enlarged cornea268158009
- MGCN - Megalocornea268158009
- Megalocornea268158009
- Cornea globular388840007
- Keratoglobus388840007
- Posterior embryotoxon392437005
- Cataract in child399336001
- Childhood cataract399336001
- Juvenile cataract399336001
- Prolapse of uvea416297003
- Uveal prolapse416297003
- Corneal thinning423459005
- Thin cornea423459005
- Peters plus syndrome449817000
- Microcephalus microcornea syndrome of Seemanova type715464002
- Microcephaly microcornea syndrome Seemanova type715464002
- Seemanova Lesny syndrome715464002
- Microcornea with corectopia and macular hypoplasia syndrome716165003
- Microcornea with glaucoma and absent frontal sinus syndrome716166002
- Cataract and microcornea syndrome722382006
- Juvenile cataract, microcornea, renal glucosuria syndrome722457005
- MRCS (microcornea, rod-cone dystrophy, cataract, posterior staphyloma) syndrome771342004
- MRCS syndrome771342004
- Microcornea, rod-cone dystrophy, cataract, posterior staphyloma syndrome771342004
- MPPC (microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma) syndrome773690008
- MPPC (microcornea, posterior megalolenticonus, persistent foetal vasculature, coloboma) syndrome773690008
- Microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma syndrome773690008
- Microcornea, posterior megalolenticonus, persistent foetal vasculature, coloboma syndrome773690008
- MMCAT (microcornea, myopic chorioretinal atrophy, telecanthus) syndrome774212003
- MMCAT syndrome774212003
- Microcornea, myopic chorioretinal atrophy, telecanthus syndrome774212003
- Megalocornea, spherophakia, secondary glaucoma syndrome783246000
- Bilateral cornea plana840485007
- Cornea plana of bilateral corneas840485007
- Cornea plana of both corneas840485007
- Bilateral microcornea866088004
- Microcornea of bilateral eyes866088004
- Ectasia of sclera870397000
- Scleral ectasia870397000
- Colobomatous macrophthalmia with microcornea syndrome1179296003
- MACOM (macrophthalmia colobomatous with microcornea) syndrome1179296003
- CCMCO - congenital cataract microcornea with corneal opacity1279837000
- Congenital cataract microcornea with corneal opacity1279837000
- Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome1303582008
- Anterior embryotoxon8041000119108
- Congenital arcus juvenilis8041000119108
- Bilateral congenital anomaly of corneas15987551000119107
- Congenital anomaly of bilateral corneas15987551000119107
- Congenital anomaly of both corneas15987551000119107
- Congenital structural abnormality of bilateral corneas15987551000119107
- Congenital structural abnormality of left cornea15987511000119106
- Congenital structural abnormality of right cornea15987591000119102
- Infantile and/or juvenile cataract342291000119102
UMLS
- Congenital malformation of cornea NOSC2910117
- Cornea of eye less than 10mm in diameterC0266544
- Cornea smallC0266544
- MicrocorneaC0266544
- Microcornea (disorder)C0266544
- MicrocorneasC0266544
- Small corneaC0266544
- Irido-corneo-trabecular dysgenesisC0344559
- Irido-corneo-trabecular dysgenesis (disorder)C0344559
- Peter anomalyC0344559
- Peter's anomalyC0344559
- Peters anomalyC0344559
- Peters congenital glaucomaC0344559
- anomalies petersC0344559
- anomaly peterC0344559
- peter's anomalyC0344559
- peters anomalyC0344559
- peters' anomalyC0344559
- Other congenital corneal malformationsC0477983
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.
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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.