Q14.0
BillableCongenital malformation of vitreous humor
Congenital malformation of vitreous humor
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital vitreous opacity
Excludes 2
Conditions not included here, but the patient may have both
- •inborn errors of metabolismE70-E88
- •cleft lip and cleft palateQ35-Q37
- •congenital malformation of cervical spine, , ,Q05.0, Q05.5, Q67.5, Q76.0-Q76.4
- •congenital malformation of larynxQ31
- •congenital malformation of lip NECQ38.0
- •congenital malformation of noseQ30
- •congenital malformation of parathyroid glandQ89.2
- •congenital malformation of thyroid glandQ89.2
- •optic nerve hypoplasiaH47.03
Related Codes(5)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(103)
SNOMED CT
- Vestigial remnants of canal of Cloquet14552009
- Vestigial remnants of hyaloid canal14552009
- Cornea small26098002
- Microcornea26098002
- Coloboma of fundus39302008
- Fundus coloboma39302008
- Persistent hyaloid artery44647001
- Posterior lenticonus95482000
- Retinal dysplasia95494009
- Congenital vitreous opacity204171005
- Lenticonus253221000
- Congenital anomaly of vitreous body253236002
- Congenital anomaly of vitreous humour253236002
- Congenital malformation of vitreous body253236002
- Congenital malformation of vitreous humor253236002
- Congenital malformation of vitreous humour253236002
- PHPV - persistent hyperplastic primary vitreous314270008
- Persistent fetal vasculature syndrome314270008
- Persistent foetal vasculature syndrome314270008
- Persistent hyperplastic primary vitreous314270008
- Hyaloid corpuscle370483001
- Mittendorf dot370483001
- Mittendorf's dot370483001
- Vitreous opacities422061002
- Vitreous opacity422061002
- Vitreoretinal dysplasia449866003
- 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
- Bilateral persistent hyperplastic primary vitreous890363003
- Persistent hyperplastic primary vitreous of bilateral eyes890363003
- Persistent hyperplastic primary vitreous of both eyes890363003
- Congenital cyst of vitreous body890415000
- Congenital vitreous cyst890415000
- Bilateral vitreous degeneration of eyes343101000119108
- Vitreous degeneration of bilateral eyes343101000119108
- Vitreous degeneration of both eyes343101000119108
- Congenital vitreous opacity of bilateral eyes15665281000119106
- Congenital vitreous opacity of both eyes15665281000119106
- Congenital vitreous opacity of left eye15665241000119101
- Congenital vitreous opacity of right eye15665201000119103
- Persistent hyperplastic primary vitreous of left eye15986831000119100
- Persistent hyperplastic primary vitreous of right eye15986871000119102
- Vitreous opacity of bilateral eyes349061000119107
- Vitreous opacity of left eye348431000119100
- Vitreous opacity of right eye347991000119105
UMLS
- Congenital anomaly of vitreous bodyC0472503
- Congenital anomaly of vitreous humourC0472503
- Congenital malformation of vitreous bodyC0472503
- Congenital malformation of vitreous humorC0472503
- Congenital malformation of vitreous humor (disorder)C0472503
- Congenital malformation of vitreous humourC0472503
- Congenital vitreous opacityC0344549
- Congenital vitreous opacity (disorder)C0344549
Clinical Terms
- Congenital vitreous cyst
- Vestigial remnants of hyaloid canal
- Congenital vitreous opacity of bilateral eyes
- Vestigial remnants of canal of Cloquet
- Persistent hyperplastic primary vitreous of bilateral eyes
- Congenital cyst of vitreous body
- Retinal dysplasia
- Congenital vitreous opacity of left eye
- Persistent hyperplastic primary vitreous of right eye
- Congenital malformation of vitreous humor (disorder)
- Vitreoretinal dysplasia
- Fundus coloboma
- Persistent hyperplastic primary vitreous
- Congenital anomaly of vitreous body
- Bilateral vitreous degeneration of eyes
- Congenital vitreous opacity
- Cornea small
- Microcornea, posterior megalolenticonus, persistent foetal vasculature, coloboma syndrome
- Vitreous opacity of bilateral eyes
- Persistent hyperplastic primary vitreous of left eye
- Vitreous opacity of left eye
- Congenital vitreous opacity (disorder)
- Mittendorf dot
- Coloboma of fundus
- Persistent foetal vasculature syndrome
- Congenital anomaly of vitreous humour
- MPPC (microcornea, posterior megalolenticonus, persistent foetal vasculature, coloboma) syndrome
- Persistent fetal vasculature syndrome
- PHPV - persistent hyperplastic primary vitreous
- Lenticonus
- Microcornea
- Vitreous opacity of right eye
- Vitreous opacity
- Persistent hyaloid artery
- Hyaloid corpuscle
- Posterior lenticonus
- Congenital vitreous opacity of right eye
- Microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma syndrome
- Mittendorf's dot
- Congenital vitreous opacity of both eyes
- Bilateral persistent hyperplastic primary vitreous
- Congenital malformation of vitreous body
- Congenital malformation of vitreous humour
- Vitreous degeneration of both eyes
- MPPC (microcornea, posterior megalolenticonus, persistent fetal vasculature, coloboma) syndrome
- Vitreous degeneration of bilateral eyes
- Vitreous opacities
- Persistent hyperplastic primary vitreous of both eyes
Frequently Asked Questions
What is the ICD-10 code for congenital malformation of vitreous humor?
The ICD-10-CM code for congenital malformation of vitreous humor is Q14.0. The full clinical description is "Congenital malformation of vitreous humor". Q14.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q14.0 mean?
ICD-10-CM code Q14.0 represents “Congenital malformation of vitreous humor”. 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 Q14.0 a billable code?
Yes, Q14.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q14.0 in?
Q14.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q14.0 map to?
Q14.0 maps to 25 SNOMED CT concepts: 890363003, 343101000119108, 39302008, 253236002, 890415000, and 20 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q14.0?
Q14.0 is linked to 2 UMLS Concept Unique Identifiers: C0472503, C0344549. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q14.0 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of vitreous humor 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 Q14.0?
Q14.0 maps to the ICD-11 code: LA13.0 (Congenital anomalies of the vitreous).
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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.