Q14.0
BillableCongenital malformation of vitreous humor
Congenital malformation of vitreous humor
Status
Billable / Specific
Parent Code
Q14Coding 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 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)
- optic nerve hypoplasia (H47.03-)
Also Known As / Clinical Terms
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
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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.