AutoICD API

Q15.9

Billable

Congenital malformation of eye, unspecified

Congenital malformation of eye, unspecified

Status

Billable / Specific

Parent Code

Q15

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Congenital anomaly of eye
  • Congenital deformity of eye

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(2)
Q15.0

Congenital glaucoma

BillableQ15.8

Other specified congenital malformations of eye

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LA1ZStructural developmental anomalies of the eye, eyelid or lacrimal apparatus, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(346)

SNOMED CT

UMLS

Clinical Terms

  • Anophthalmia-Waardenburg syndrome
  • Axonal neuropathy
  • Anophthalmia with pulmonary hypoplasia syndrome
  • Oculootoradial syndrome
  • CODAS (cerebro-oculo-dento-auriculo-skeletal) syndrome
  • Posterior fossa brain malformation, haemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
  • Hypohidrotic ectodermal dysplasia, hypothyroidism, ciliary dyskinesia syndrome
  • Eye Abnormality
  • Congenital anomaly of eye, ear and neck
  • Conductive hearing loss of right ear
  • Steroid-resistant nephrotic syndrome
  • Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome
  • Joubert syndrome
  • Syndromic microphthalmia type 9
  • Oculo-palato-cerebral syndrome
  • OGIN syndrome
  • RAB18 deficiency
  • Syndactyly-anophthalmos syndrome
  • Unspecified anomaly of eye, congenital
  • Mixed conductive and sensorineural hearing loss of left ear
  • Congenital deformity of eye
  • IVIC syndrome
  • Mixed conductive and sensorineural deafness
  • Congenital malformation of eye, ear and neck
  • Median cleft face syndrome
  • Mixed deafness
  • RAB18, member RAS oncogene family deficiency
  • Delleman-Oorthuys syndrome
  • Eye abnormalities
  • congenital diseases eye
  • Ocular anomalies, axonal neuropathy, developmental delay syndrome
  • Congenital anomaly of ocular adnexa
  • Familial juvenile nephronophthisis
  • Congenital eye disorder
  • Cerebro-oculo-dento-auriculo-skeletal syndrome
  • Feingold syndrome
  • Mixed conductive AND sensorineural hearing loss
  • Autosomal recessive medullary cystic disease
  • Harel Yoon syndrome
  • Waardenburg anophthalmia syndrome
  • Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome
  • Hereditary cerebellar atrophy
  • MHL - Mixed hearing loss
  • Familial aplasia of the vermis
  • Congenital eye malformations
  • Auricular abnormality, cleft lip, ocular abnormality syndrome
  • ANOTHER syndrome
  • Cerebello-oculo-renal syndrome
  • Arima syndrome
  • Choanal atresia
  • Conductive hearing loss, bilateral
  • Congenital hypotrichosis
  • Dysplasia with defective mineralization
  • Oculoauricular syndrome Schorderet type
  • Pascual Castroviejo syndrome type 2
  • Familial juvenile medullary cystic kidney disease
  • Oculo-palato-cerebral dwarfism
  • Abnormality, Eye
  • Congenital abnormality of eye
  • Hypotrichosis congenita
  • Eye deformity congenital NOS
  • anomalies eye
  • Oculo-oto-radial syndrome
  • OAFNS - oculoauriculofrontonasal syndrome
  • MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 3
  • Congenital atresia of choana
  • Joubert syndrome with oculorenal defect
  • Marles-Greenburg-Persaud syndrome
  • Muscle eye brain disease with bilateral multicystic leucodystrophy
  • Dysplasia with defective mineralisation
  • SYT1-related neurodevelopmental disorder
  • Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome
  • PHPV - persistent hyperplastic primary vitreous
  • Oculo-digito-esophagoduodenal syndrome
  • Manitoba oculotrichoanal syndrome
  • Oculogastrointestinal neurodevelopmental syndrome
  • Microcephaly-oculo-digito-oesophageal-duodenal syndrome
  • Oculocerebrocutaneous syndrome
  • MOMO (macrocephaly, obesity, mental disability, ocular abnormality) syndrome
  • Marles syndrome
  • MOMO syndrome
  • Congenital eye deformity NOS
  • Atresia of posterior nares
  • Eye malformation
  • Muscle eye brain disease with bilateral multicystic leukodystrophy
  • Mixed conductive and sensorineural hearing loss of right ear
  • MOTA - Manitoba oculotrichoanal syndrome
  • eye malformations
  • Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome
  • Anophthalmos with limb anomalies
  • Matthew Wood syndrome
  • Oculoauriculofrontonasal syndrome
  • EYE ABNORM
  • Oculo-cerebro-dental syndrome
  • Atresia of posterior naris
  • Steroid-unresponsive nephrotic syndrome
  • Intractable diarrhoea with choanal atresia and eye anomaly syndrome
  • Baker Gordon syndrome
  • Congenital hypotrichia
  • PHACE syndrome
  • Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
  • Intractable diarrhea with choanal atresia and eye anomaly syndrome
  • Congenital anomaly of eye
  • CODAS syndrome
  • Mixed conductive and sensorineural hearing loss, bilateral
  • Congenital atresia of posterior nares
  • Oculopalatocerebral syndrome
  • Combined malformation of central nervous system and skeletal muscle
  • Sensorineural hearing loss of bilateral ears
  • Chronic diarrhoea of infants AND/OR young children
  • Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
  • Nephronophthisis
  • RHOA (ras homolog family member A) related mosaic ectodermal dysplasia
  • Anophthalmia-syndactyly
  • Ophthalmologic abnormalities
  • Sensorineural hearing loss of both ears
  • Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome
  • RHOA-related mosaic ectodermal dysplasia
  • IVIC (Instituto Venezolano de Investigaciones Cientificas) syndrome
  • congenital eye syndrome
  • Pierson syndrome
  • MOMES syndrome
  • Acro-renal-ocular syndrome
  • Bilateral hearing loss
  • Glaucoma due to congenital anomaly of eye
  • Anophthalmos-limb anomalies syndrome
  • Congenital anomaly of eye (disorder)
  • Frontonasal dysplasia sequence
  • Congenital mixed conductive and sensorineural hearing loss
  • GPAA1-related biosynthesis defect
  • Synaptotagmin 1-related neurodevelopmental disorder
  • Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome
  • Acrorenoocular syndrome
  • Eye abnormality NOS
  • ANOTHER (alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy, respiratory tract infection) syndrome
  • Conductive hearing loss of left ear
  • Aplasia cutis congenita secondary to malformation syndrome (Type 9)
  • Oculocerebrodental syndrome
  • Eye disorders congenital
  • Microcephaly-oculo-digito-esophageal-duodenal syndrome
  • Infantile hemangioma
  • Chronic diarrhea of infants AND/OR young children
  • Microcoria and congenital nephrosis syndrome
  • Congenital anomaly of the globe
  • SRNS - Steroid-resistant nephrotic syndrome
  • Macrocephaly, obesity, mental disability, ocular abnormality syndrome
  • Infantile haemangioma
  • Congenital disorder of glycosylation due to PIGT deficiency
  • Mixed hearing loss
  • Persistent hyperplastic primary vitreous
  • Microphthalmia with limb anomalies
  • congenital disorder eye
  • Persistent foetal vasculature syndrome
  • Persistent fetal vasculature syndrome
  • Oculo-digito-oesophagoduodenal syndrome
  • Congenital disorder of glycosylation due to PIGT (phosphatidylinositol glycan anchor biosynthesis class T) deficiency
  • Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections
  • Glycosylphosphatidylinositol anchor attachment 1-related biosynthesis defect
  • Abnormalities, Eye
  • Ophthalmo-acromelic syndrome
  • Mixed type deafness
  • Ophthalmoacromelic syndrome
  • Congenital eye anomalies
  • abnormalities eye
  • Upper limb defect with eye and ear abnormalities syndrome
  • Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome
Frequently Asked Questions
What is the ICD-10 code for congenital malformation of eye, unspecified?

The ICD-10-CM code for congenital malformation of eye, unspecified is Q15.9. The full clinical description is "Congenital malformation of eye, unspecified". Q15.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q15.9 mean?

ICD-10-CM code Q15.9 represents “Congenital malformation of eye, unspecified”. 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 Q15.9 a billable code?

Yes, Q15.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q15.9 in?

Q15.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q15.9?

Q15.9 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital nystagmus (H55.01); ocular albinism (E70.31-); optic nerve hypoplasia (H47.03-); and 1 more.

What SNOMED CT codes does Q15.9 map to?

Q15.9 maps to 60 SNOMED CT concepts: 239050000, 720415006, 722458000, 703403003, 403553002, and 55 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q15.9?

Q15.9 is linked to 1 UMLS Concept Unique Identifier: C0015393. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q15.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of eye, unspecified 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 Q15.9?

Q15.9 maps to the ICD-11 code: LA1Z (Structural developmental anomalies of the eye, eyelid or lacrimal apparatus, unspecified).

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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.