Cleft iris
Disorder of cholesterol metabolism
Congenital zonular cataract of left eye
Congenital posterior subcapsular polar cataract of both eyes
Left congenital capsular cataract
Congenital cataract, progressive muscular hypotonia, deafness, developmental delay syndrome
Congenital posterior subcapsular polar cataract
cataracts congenital
Congenital glaucoma of left eye
Cortical and zonular cataract
Bilateral congenital posterior subcapsular polar cataracts of eyes
Left ventricular myocardial noncompaction cardiomyopathy
Bilateral congenital nuclear cataracts of eyes
Congenital capsular cataract of left eye
Congenital cataract of left eye
Congenital coloboma of bilateral irides
RAB18 deficiency
Familial keratoconus with cataract
Primrose syndrome
Anterior subcapsular polar cataract of left eye
Congenital anomaly of anterior pituitary
Congenital subcapsular cataract
Atresia ani
Congenital porencephalia
Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome
Cornea small
EDICT (endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning) syndrome
HCC - hypomyelination and congenital cataract
Lubinsky syndrome
Right congenital anterior subcapsular polar cataract
Nathalie syndrome
Congenital cataract of both eyes
Intellectual disability, cataract, calcified pinna, myopathy syndrome
Developmental cataract
CCFDN - congenital cataracts, facial dysmorphism and neuropathy
Aproctia
Congenital cataract with intellectual disability and anal atresia and urinary defect syndrome
Hutterite type cataract
Mature cataract
Anterior subcapsular cataract of both eyes
Microcornea
RAB18, member RAS oncogene family deficiency
Crome syndrome
Cataract of lens capsule of bilateral eyes
Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts
Distal spinal muscular atrophy
Congenital cataract with hypertrichosis and intellectual disability syndrome
Cataract and testicular failure syndrome
Congenital posterior polar cataract
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome
Congenital coloboma of iris of left eye
Posterior subcapsular polar cataract
Schaap Taylor Baraitser syndrome
Ventricular myocardial noncompaction cardiomyopathy
Cataract with aberrant oral frenula and growth delay syndrome
Lamellar cataract
Nuclear cataract
Sterol-C4-methyl oxidase deficiency
EFE - Endocardial fibroelastosis
Congenital anterior subcapsular polar cataract
Congenital nuclear cataract of left eye
Congenital zonular cataract of both eyes
Congenital cataract, nephropathy, encephalopathy syndrome
Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome
Congenital combined form cataract of both eyes
Congenital cataract microcornea with corneal opacity
Congenital sutural cataract
Congenital cerebral porosis
Hypertrophic mitochondrial cardiomyopathy
Left congenital glaucoma
Congenital posterior subcapsular polar cataract of bilateral eyes
Inborn error of lipoprotein metabolism
Congenital capsular cataract
Total cataract
Congenital capsular cataract of bilateral eyes
Coralliform cataract
EDICT syndrome
Congenital cataract, hearing loss, severe developmental delay syndrome
Endocardial fibroelastosis
Cataract of posterior subcapsule of left eye
Congenital blue dot cataract
Cataract and microcornea syndrome
Cerulean cataract
Cataract, congenital
Bilateral posterior subcapsular cataract
Anterior subcapsular cataract of right eye
Pulverulent cataract
Congenital lamellar cataract
Spastic paraparesis, cataracts, speech delay syndrome
Congenital combined form cataract of right eye
Cataract glaucoma syndrome
Congenital cataract with deafness and hypogonadism syndrome
Right congenital nuclear cataract
Elastomyofibrosis
Congenital atresia of anus
Anterior subcapsular cataract of left eye
Hydrocephalus with endocardial fibroelastosis and cataract syndrome
Congenital zonular cataract of right eye
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
Absence deformity of leg and congenital cataract syndrome
CAHMR syndrome
Osteogenesis imperfecta, type II
Cataract of posterior subcapsule of right eye
Sengers syndrome
Congenital cortical cataract
Bilateral congenital cataract of eyes
Cataract, congenital heart disease, neural tube defect syndrome
Congenital nuclear cataract of bilateral eyes
Congenital cortical cataract of right eye
Martsolf-like syndrome
Lethal osteogenesis imperfecta
ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
Notched iris
Congenital cataracts
Congenital complete cataract
Imperforate anus
Cataracts, congenital
Congenital nuclear cataract
Bilateral anterior subcapsular polar cataract
Congenital glaucoma of both eyes
Congenital porencephaly
cataract congenital
Cortical cataract - congenital
Fibroelastosis cordis
Bilateral congenital capsular cataracts
Congenital nuclear cataract of both eyes
Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement
Congenital capsular cataract of right eye
Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome
Porencephaly, microcephaly, bilateral congenital cataract syndrome
Congenital zonular cataract
Left congenital posterior subcapsular polar cataract
Congenital cataract (disorder)
Dandy-Walker malformation
Congenital coloboma of iris
Congenital total cataract
Bilateral congenital combined form cataracts
HEC (hydrocephalus, endocardial fibroelastosis, cataract) syndrome
Congenital posterior subcapsular polar cataract of left eye
Congenital zonular cataract of bilateral eyes
Left congenital combined form cataract
Dandy-Walker deformity
Congenital anterior subcapsular polar cataract of bilateral eyes
Congenital nuclear cataract of right eye
Anterior subcapsular polar cataract of right eye
Anterior subcapsular polar cataract of both eyes
Congenital cataract of right eye
CAHMR (cataract, hypertrichosis, mental retardation) syndrome
Congenital cataract, unspecified
Congenital cataract, deafness, severe developmental delay syndrome
Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome
Congenital anterior subcapsular polar cataract of right eye
Posterior subcapsular cataract of both eyes
Right congenital capsular cataract
Clouding of the lens of the eye at birth
Congenital cataracts, facial dysmorphism and neuropathy
Congenital imperforate anus
Embryonal nuclear cataract
Congenital anterior polar cataract
Hypomyelination and congenital cataract
Karandikar Maria Kamble syndrome
Lethal neurodegenerative disorder due to copper transport defect
Osteogenesis imperfecta, perinatal lethal
Congenital cortical cataract of left eye
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
Bilateral congenital combined form cataract of eyes
Posterior subcapsular cataract of right eye
Bilateral congenital anterior subcapsular polar cataracts
Congenital coloboma of iris of right eye
Posterior subcapsular cataract of left eye
Calcification of pinna
Congenital endocardial fibroelastosis
Psoriasiform dermatitis
Hypergonadotropic hypogonadism with cataract syndrome
Congenital membranous cataract
Anterior subcapsular polar cataract of bilateral eyes
Congenital capsular cataract of both eyes
Congenital polar cataract
Congenital posterior subcapsular polar cataract of right eye
Wellesley Carman French syndrome
Congenital anterior subcapsular polar cataract of both eyes
HEC syndrome
Embryonal nuclear cataract of right eye
Bilateral congenital cortical cataract of eyes
Congenital combined form cataract of bilateral eyes
Congenital combined form cataract of left eye
Endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning syndrome
Fatty acyl-CoA reductase 1 superactivity
NS - Nuclear sclerosis
Schizencephalic porencephaly
CCMCO - congenital cataract microcornea with corneal opacity
Spondyloepiphyseal dysplasia Nishimura type
Left congenital nuclear cataract
Right congenital combined form cataract
Congenital cortical cataract of both eyes
Congenital combined form cataract
Osteogenesis imperfecta type II
Right congenital posterior subcapsular polar cataract
Congenital glaucoma of right eye
Congenital anterior subcapsular polar cataract of left eye
Embryonal nuclear cataract of left eye
Congenital coloboma of both irises
Anterior subcapsular cataract of bilateral eyes
Anal atresia
Dandy-Walker syndrome
Deafness with cataract and skeletal anomaly syndrome
SMO (sterol-C4-methyl oxidase) deficiency
Bilateral congenital zonular cataract
Congenital cataract ichthyosis syndrome
Congenital glaucoma of bilateral eyes
Punctate cataract
Autosomal dominant keratoconus with early-onset anterior polar cataract
Pinnal calcification
Right congenital glaucoma
Congenital malformation of anterior pituitary
Disorder of cholesterol synthesis
Congenital cataract of bilateral eyes
Left congenital anterior subcapsular polar cataract
Congenital cortical cataract of bilateral eyes
Martsolf syndrome
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome
Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome
Congenital cataract with ataxia and deafness syndrome
Cataract of posterior subcapsule of bilateral eyes

Frequently Asked Questions

What is the ICD-10 code for congenital cataract?

The ICD-10-CM code for congenital cataract is Q12.0. The full clinical description is "Congenital cataract". Q12.0 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q12.0 mean?

ICD-10-CM code Q12.0 represents “Congenital cataract”. 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 Q12.0 a billable code?

Yes, Q12.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q12.0 in?

Q12.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What SNOMED CT codes does Q12.0 map to?

Q12.0 maps to 117 SNOMED CT concepts: 716099003, 204712000, 15737801000119107, 15737841000119109, 15737761000119104, and 112 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q12.0?

Q12.0 is linked to 1 UMLS Concept Unique Identifier: C0009691. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q12.0 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital cataract 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 Q12.0?

Q12.0 maps to the ICD-11 code: LA12.1 (Congenital cataract).

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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.