ICD-10 Diagnosis Code Q12.0

Congenital cataract

Diagnosis Code Q12.0

ICD-10: Q12.0
Short Description: Congenital cataract
Long Description: Congenital cataract
This is the 2019 version of the ICD-10-CM diagnosis code Q12.0

Valid for Submission
The code Q12.0 is valid for submission for HIPAA-covered transactions.

Code Classification
  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Congenital malformations of eye, ear, face and neck (Q10-Q18)
      • Congenital lens malformations (Q12)

Information for Medical Professionals

Diagnostic Related Groups
The diagnosis code Q12.0 is grouped in the following Diagnostic Related Group(s) (MS-DRG V35.0)

  • 124 - OTHER DISORDERS OF THE EYE WITH MCC
  • 125 - OTHER DISORDERS OF THE EYE WITHOUT MCC

Convert to ICD-9 Additional informationCallout TooltipGeneral Equivalence Map
The ICD-10 and ICD-9 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.

Present on Admission (POA) Additional informationCallout TooltipPresent on Admission
The Present on Admission (POA) indicator is used for diagnosis codes included in claims involving inpatient admissions to general acute care hospitals. POA indicators must be reported to CMS on each claim to facilitate the grouping of diagnoses codes into the proper Diagnostic Related Groups (DRG). CMS publishes a listing of specific diagnosis codes that are exempt from the POA reporting requirement.

The code Q12.0 is exempt from POA reporting.

Synonyms
  • Absence deformity of leg and congenital cataract syndrome
  • Anal atresia
  • Anterior subcapsular cataract
  • Anterior subcapsular polar cataract
  • Capsular cataract
  • Cataract and microcornea syndrome
  • Cataract glaucoma syndrome
  • Cataract, congenital heart disease, neural tube defect syndrome
  • Congenital anterior polar cataract
  • Congenital anterior polar cataract
  • Congenital anterior subcapsular polar cataract
  • Congenital blue dot cataract
  • Congenital capsular and/or subcapsular cataract
  • Congenital capsular cataract
  • Congenital cataract
  • Congenital cataract and lens anomalies
  • Congenital cataract ichthyosis syndrome
  • Congenital cataract with ataxia and deafness syndrome
  • Congenital cataract with deafness and hypogonadism syndrome
  • Congenital cataract with hypertrichosis and intellectual disability syndrome
  • Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
  • Congenital cataracts, facial dysmorphism and neuropathy
  • Congenital combined form cataract
  • Congenital cortical cataract
  • Congenital hypertrichosis
  • Congenital hypogonadotropic hypogonadism
  • Congenital kyphosis
  • Congenital lamellar cataract
  • Congenital membranous cataract
  • Congenital polar cataract
  • Congenital polar cataract
  • Congenital posterior polar cataract
  • Congenital posterior subcapsular polar cataract
  • Congenital subcapsular cataract
  • Congenital subtotal cataract
  • Congenital sutural cataract
  • Congenital total cataract
  • Congenital zonular cataract
  • Cortical and zonular cataract
  • Cortical cataract
  • Crome syndrome
  • Dandy-Walker syndrome
  • Disorder of endocardium and heart valve
  • Distal spinal muscular atrophy
  • EDICT syndrome
  • Embryonal nuclear cataract
  • Endocardial fibroelastosis
  • Hydrocephalus with endocardial fibroelastosis and cataract syndrome
  • Hypergonadotropic hypogonadism with cataract syndrome
  • Hypertrophic mitochondrial cardiomyopathy
  • Hypomyelination and congenital cataract
  • Intellectual disability with cataract and kyphosis syndrome
  • Intellectual disability, cataract, calcified pinna, myopathy syndrome
  • Irido-corneal dysgenesis
  • Karandikar Maria Kamble syndrome
  • Martsolf syndrome
  • Mature cataract
  • Microcornea
  • Mitochondrial cardiomyopathy
  • Nathalie syndrome
  • Nuclear cataract
  • Osteogenesis imperfecta, perinatal lethal
  • Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts
  • Pinnal calcification
  • Posterior subcapsular polar cataract
  • Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome
  • Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome
  • Total and subtotal congenital cataract
  • Wellesley Carman French syndrome

Information for Patients


Birth Defects

A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.

A birth defect may affect how the body looks, works or both. Some birth defects like cleft lip or neural tube defects are structural problems that can be easy to see. To find others, like heart defects, doctors use special tests. Birth defects can range from mild to severe. Causes can include

  • Genetics
  • Exposures to medicines or chemicals. For example, alcohol abuse can cause fetal alcohol syndrome.
  • Infections during pregnancy
  • Certain medicines. Before you get pregnant, talk to your health care provider about any medicines you take.
  • Not getting enough of certain nutrients. For example, not getting enough folic acid before and during pregnancy is a key factor in causing neural tube defects.

For most birth defects, the cause is unknown.

Health care providers can diagnose certain birth defects during pregnancy, with prenatal tests. That's why it important to get regular prenatal care. Other birth defects may not be found until after the baby is born. Sometimes the defect is obvious right away. Other times, the health care provider may not discover it until later in life.

Babies with birth defects often need special care and treatments. The treatments may include surgery, medicines, assistive devices, and therapies.

Centers for Disease Control and Prevention

  • Intersex (Medical Encyclopedia)


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Eye Diseases

Some eye problems are minor and don't last long. But some can lead to a permanent loss of vision.

Common eye problems include

  • Refractive errors
  • Cataracts - clouded lenses
  • Optic nerve disorders, including glaucoma
  • Retinal disorders - problems with the nerve layer at the back of the eye
  • Macular degeneration - a disease that destroys sharp, central vision
  • Diabetic eye problems
  • Conjunctivitis - an infection also known as pinkeye

Your best defense is to have regular checkups, because eye diseases do not always have symptoms. Early detection and treatment could prevent vision loss. See an eye care professional right away if you have a sudden change in vision, if everything looks dim, or if you see flashes of light. Other symptoms that need quick attention are pain, double vision, fluid coming from the eye, and inflammation.

NIH: National Eye Institute

  • Anisocoria (Medical Encyclopedia)
  • Choroidal dystrophies (Medical Encyclopedia)
  • Coloboma of the iris (Medical Encyclopedia)
  • Episcleritis (Medical Encyclopedia)
  • Eye and orbit ultrasound (Medical Encyclopedia)
  • Eye burning - itching and discharge (Medical Encyclopedia)
  • Eye pain (Medical Encyclopedia)
  • Eye redness (Medical Encyclopedia)
  • Fluorescein angiography (Medical Encyclopedia)
  • Fluorescein eye stain (Medical Encyclopedia)
  • Heterochromia (Medical Encyclopedia)
  • Ophthalmoscopy (Medical Encyclopedia)
  • Orbit CT scan (Medical Encyclopedia)
  • Orbital pseudotumor (Medical Encyclopedia)
  • Photophobia (Medical Encyclopedia)
  • Pinguecula (Medical Encyclopedia)
  • Pterygium (Medical Encyclopedia)
  • Pupil - white spots (Medical Encyclopedia)
  • Scleritis (Medical Encyclopedia)
  • Slit-lamp exam (Medical Encyclopedia)
  • Standard ophthalmic exam (Medical Encyclopedia)
  • Subconjunctival hemorrhage (Medical Encyclopedia)
  • Uveitis (Medical Encyclopedia)


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