Q15.9
BillableCongenital malformation of eye, unspecified
Congenital malformation of eye, unspecified
Status
Billable / Specific
Parent Code
Q15Coding 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
- 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)
Also Known As / Clinical Terms
SNOMED CT
- Congenital abnormality of eye19416009
- Congenital anomaly of eye19416009
- Congenital anomaly of the globe19416009
- Congenital deformity of eye19416009
- Congenital eye anomalies19416009
- Congenital malformation of eye19416009
- Chronic diarrhea of infants AND/OR young children25319005
- Chronic diarrhoea of infants AND/OR young children25319005
- Congenital hypotrichia56558005
- Congenital hypotrichosis56558005
- Hypotrichosis congenita56558005
- Axonal neuropathy60703000
- MHL - Mixed hearing loss77507001
- Mixed conductive AND sensorineural hearing loss77507001
- Mixed conductive and sensorineural deafness77507001
- Mixed deafness77507001
- Mixed hearing loss77507001
- Mixed type deafness77507001
- Frontonasal dysplasia sequence86610004
- Median cleft face syndrome86610004
- Bilateral hearing loss95820000
- Congenital anomaly of ocular adnexa128327004
- Conductive hearing loss, bilateral194417009
- Sensorineural hearing loss of bilateral ears194424005
- Sensorineural hearing loss of both ears194424005
- Mixed conductive and sensorineural hearing loss, bilateral194429000
- Atresia of posterior nares204508009
- Atresia of posterior naris204508009
- Choanal atresia204508009
- Congenital atresia of choana204508009
- Congenital atresia of posterior nares204508009
- Autosomal recessive medullary cystic disease204958008
- Familial juvenile medullary cystic kidney disease204958008
- Familial juvenile nephronophthisis204958008
- Nephronophthisis204958008
- SRNS - Steroid-resistant nephrotic syndrome236381000
- Steroid-resistant nephrotic syndrome236381000
- Steroid-unresponsive nephrotic syndrome236381000
- ANOTHER (alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy, respiratory tract infection) syndrome239050000
- ANOTHER syndrome239050000
- Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections239050000
- Hypohidrotic ectodermal dysplasia, hypothyroidism, ciliary dyskinesia syndrome239050000
- Familial aplasia of the vermis253175003
- Congenital anomaly of eye, ear and neck253204009
- Congenital malformation of eye, ear and neck253204009
- Dysplasia with defective mineralisation254117007
- Dysplasia with defective mineralization254117007
- Combined malformation of central nervous system and skeletal muscle277949001
- PHPV - persistent hyperplastic primary vitreous314270008
- Persistent fetal vasculature syndrome314270008
- Persistent foetal vasculature syndrome314270008
- Persistent hyperplastic primary vitreous314270008
- Aplasia cutis congenita secondary to malformation syndrome (Type 9)403553002
- Delleman-Oorthuys syndrome403554008
- Oculocerebrocutaneous syndrome403554008
- PHACE syndrome698765007
- Pascual Castroviejo syndrome type 2698765007
- Posterior fossa brain malformation, haemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome698765007
- Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome698765007
- Feingold syndrome702431004
- Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome702431004
- Microcephaly-oculo-digito-esophageal-duodenal syndrome702431004
- Microcephaly-oculo-digito-oesophageal-duodenal syndrome702431004
- Oculo-digito-esophagoduodenal syndrome702431004
- Oculo-digito-oesophagoduodenal syndrome702431004
- Anophthalmia-Waardenburg syndrome703403003
- Anophthalmia-syndactyly703403003
- Anophthalmos with limb anomalies703403003
- Anophthalmos-limb anomalies syndrome703403003
- Microphthalmia with limb anomalies703403003
- Ophthalmo-acromelic syndrome703403003
- Ophthalmoacromelic syndrome703403003
- Syndactyly-anophthalmos syndrome703403003
- Waardenburg anophthalmia syndrome703403003
- MOTA - Manitoba oculotrichoanal syndrome703539006
- Manitoba oculotrichoanal syndrome703539006
- Marles syndrome703539006
- Marles-Greenburg-Persaud syndrome703539006
- Upper limb defect with eye and ear abnormalities syndrome716110002
- Joubert syndrome716997004
- CODAS (cerebro-oculo-dento-auriculo-skeletal) syndrome717772000
- CODAS syndrome717772000
- Cerebro-oculo-dento-auriculo-skeletal syndrome717772000
- Intractable diarrhea with choanal atresia and eye anomaly syndrome720009004
- Intractable diarrhoea with choanal atresia and eye anomaly syndrome720009004
- Acro-renal-ocular syndrome720415006
- Acrorenoocular syndrome720415006
- Arima syndrome721862000
- Cerebello-oculo-renal syndrome721862000
- Joubert syndrome with oculorenal defect721862000
- IVIC (Instituto Venezolano de Investigaciones Cientificas) syndrome722019000
- IVIC syndrome722019000
- Oculo-oto-radial syndrome722019000
- Oculootoradial syndrome722019000
- Oculo-palato-cerebral dwarfism722055008
- Oculo-palato-cerebral syndrome722055008
- Oculopalatocerebral syndrome722055008
- Anophthalmia with pulmonary hypoplasia syndrome722458000
- Matthew Wood syndrome722458000
- Syndromic microphthalmia type 9722458000
- Microcoria and congenital nephrosis syndrome723449004
- Pierson syndrome723449004
- MOMO (macrocephaly, obesity, mental disability, ocular abnormality) syndrome724137002
- MOMO syndrome724137002
- Macrocephaly, obesity, mental disability, ocular abnormality syndrome724137002
- Auricular abnormality, cleft lip, ocular abnormality syndrome725149008
- Congenital mixed conductive and sensorineural hearing loss737377004
- Oculoauricular syndrome Schorderet type763815000
- Congenital disorder of glycosylation due to PIGT (phosphatidylinositol glycan anchor biosynthesis class T) deficiency770755007
- Congenital disorder of glycosylation due to PIGT deficiency770755007
- Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome770755007
- MCAHS (multiple congenital anomalies, hypotonia, seizures syndrome) type 3770755007
- RAB18 deficiency772225005
- RAB18, member RAS oncogene family deficiency772225005
- Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome774102003
- MOMES syndrome774102003
- OAFNS - oculoauriculofrontonasal syndrome782783009
- Oculoauriculofrontonasal syndrome782783009
- Muscle eye brain disease with bilateral multicystic leucodystrophy785298001
- Muscle eye brain disease with bilateral multicystic leukodystrophy785298001
- Glaucoma due to congenital anomaly of eye1003428009
- Conductive hearing loss of right ear1010236009
- Conductive hearing loss of left ear1010238005
- Harel Yoon syndrome1172586007
- Ocular anomalies, axonal neuropathy, developmental delay syndrome1172586007
- Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome1172630000
- Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies1208985003
- RHOA (ras homolog family member A) related mosaic ectodermal dysplasia1208985003
- RHOA-related mosaic ectodermal dysplasia1208985003
- Baker Gordon syndrome1217371005
- Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome1217371005
- SYT1-related neurodevelopmental disorder1217371005
- Synaptotagmin 1-related neurodevelopmental disorder1217371005
- GPAA1-related biosynthesis defect1217381009
- Glycosylphosphatidylinositol anchor attachment 1-related biosynthesis defect1217381009
- Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome1217381009
- Oculo-cerebro-dental syndrome1255268002
- Oculocerebrodental syndrome1255268002
- Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome1279889005
- Infantile haemangioma1293125002
- Infantile hemangioma1293125002
- OGIN syndrome1356735003
- Oculogastrointestinal neurodevelopmental syndrome1356735003
- Hereditary cerebellar atrophy431641000124107
- Mixed conductive and sensorineural hearing loss of left ear18701000119107
- Mixed conductive and sensorineural hearing loss of right ear18711000119105
UMLS
- Abnormalities, EyeC0015393
- Abnormality, EyeC0015393
- Congenital Eye DisorderC0015393
- Congenital abnormality of eyeC0015393
- Congenital anomaly of eyeC0015393
- Congenital anomaly of eye (disorder)C0015393
- Congenital anomaly of the globeC0015393
- Congenital deformity of eyeC0015393
- Congenital eye anomaliesC0015393
- Congenital eye deformity NOSC0015393
- Congenital eye disorderC0015393
- Congenital eye malformationsC0015393
- Congenital malformation of eyeC0015393
- Congenital malformation of eye, unspecifiedC0015393
- EYE ABNORMC0015393
- Eye AbnormalitiesC0015393
- Eye AbnormalityC0015393
- Eye abnormalitiesC0015393
- Eye abnormalityC0015393
- Eye abnormality NOSC0015393
- Eye deformity congenital NOSC0015393
- Eye disorders congenitalC0015393
- Eye malformationC0015393
- Ophthalmologic abnormalitiesC0015393
- Unspecified anomaly of eye, congenitalC0015393
- abnormalities eyeC0015393
- anomalies eyeC0015393
- congenital diseases eyeC0015393
- congenital disorder eyeC0015393
- congenital eye disorderC0015393
- congenital eye syndromeC0015393
- eye abnormalitiesC0015393
- eye abnormalityC0015393
- eye malformationsC0015393
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.
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.