Q13.0
BillableColoboma of iris
Coloboma of iris
Status
Billable / Specific
Parent Code
Q13Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Coloboma NOS
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
- Complete deafness8531006
- Cornea small26098002
- Microcornea26098002
- Congenital small ears35045004
- Microtia35045004
- Coloboma of fundus39302008
- Fundus coloboma39302008
- Congenital coloboma of optic disc44295002
- Congenital optic disc coloboma44295002
- Cleft iris51485001
- Congenital coloboma of iris51485001
- Notched iris51485001
- MHL - Mixed hearing loss77507001
- Mixed conductive AND sensorineural hearing loss77507001
- Mixed conductive and sensorineural deafness77507001
- Mixed deafness77507001
- Mixed hearing loss77507001
- Mixed type deafness77507001
- Macrophthalmia93181004
- Macrophthalmos93181004
- Megalophthalmia93181004
- Megalophthalmos93181004
- Megalophthalmus93181004
- COI - Coloboma of iris, choroid and retina93390002
- Coloboma of eye93390002
- Coloboma of iris, choroid and retina93390002
- Congenital ocular coloboma93390002
- Ocular coloboma93390002
- Congenital deafness95828007
- X-linked sensorineural hearing loss232329002
- Android fat distribution248311001
- Central obesity248311001
- Centripetal obesity248311001
- Fat body with thin limbs248311001
- Obesity of face and trunk, sparing limbs248311001
- Truncal obesity248311001
- Atresia of nasolacrimal duct278530008
- Papillorenal syndrome446449009
- Renal coloboma syndrome446449009
- Colobomatous microphthalmia715771008
- Microphthalmia with colobomatous cyst715771008
- Microphthalmos co-occurrent with congenital ocular coloboma715771008
- Biemond syndrome type 2717887003
- Abruzzo Erickson syndrome718574003
- CHARGE-like syndrome718574003
- Cleft palate with coloboma of eye and deafness syndrome718574003
- Uveal coloboma with cleft lip and palate and intellectual disability syndrome719042007
- Craniofacial dysmorphism with coloboma of eye and corpus callosum agenesis syndrome719947004
- Temtamy Shalash syndrome719947004
- Temtamy syndrome719947004
- CHIME (coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability, ear anomaly) syndrome720639008
- CHIME syndrome720639008
- Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome720639008
- Neuroectodermal dysplasia CHIME type720639008
- Zunich Kaye syndrome720639008
- Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome722282008
- Graham Cox syndrome722282008
- Balikova Vermeesch syndrome724139004
- Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome724139004
- Pfeiffer Mayer syndrome733088002
- Preaxial polydactyly, colobomata, intellectual disability syndrome733088002
- Congenital mixed conductive and sensorineural hearing loss737377004
- X-linked cerebral, cerebellar, coloboma syndrome770604006
- X-linked intellectual disability Kroes type770604006
- Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome776204008
- Bilateral colobomatous microphthalmia840492002
- Bilateral microphthalmos with congenital coloboma840492002
- Microphthalmos co-occurrent with congenital ocular coloboma of bilateral eyes840492002
- Microphthalmos with congenital ocular coloboma of both eyes840492002
- Familial progressive retinal dystrophy, iris coloboma, congenital cataract syndrome1172636006
- Colobomatous macrophthalmia with microcornea syndrome1179296003
- MACOM (macrophthalmia colobomatous with microcornea) syndrome1179296003
- COMMAD (coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness) syndrome1332382002
- COMMAD syndrome1332382002
- Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome1332382002
- Bilateral microphthalmos15987151000119103
- Microphthalmos of bilateral eyes15987151000119103
- Microphthalmos of both eyes15987151000119103
- Congenital coloboma of bilateral irides15665721000119102
- Congenital coloboma of both irises15665721000119102
- Congenital coloboma of iris of left eye15665761000119107
- Congenital coloboma of iris of right eye15665681000119108
- Microphthalmia of left eye15987231000119104
- Microphthalmos of left eye15987231000119104
- Microphthalmia of right eye15987191000119108
- Microphthalmos of right eye15987191000119108
UMLS
- COI - Coloboma of iris, choroid and retinaC0009363
- COLOBOMA, OCULARC0009363
- ColobomaC0009363
- Coloboma NOSC0009363
- Coloboma Of Iris, Choroid, And RetinaC0009363
- Coloboma of eyeC0009363
- Coloboma of iris, choroid and retinaC0009363
- Coloboma of iris, choroid, and retinaC0009363
- Coloboma of iris, retina, and choroidC0009363
- Coloboma of the EyeC0009363
- Coloboma, OcularC0009363
- ColobomasC0009363
- Colobomas, OcularC0009363
- ColobomataC0009363
- Congenital ocular colobomaC0009363
- Congenital ocular coloboma (disorder)C0009363
- Eye colobomaC0009363
- Notched pupilC0009363
- Ocular ColobomaC0009363
- Ocular ColobomasC0009363
- Ocular colobomaC0009363
- Ocular colobomasC0009363
- colobomaC0009363
- coloboma eyeC0009363
- colobomasC0009363
- colobomataC0009363
- ocular colobomaC0009363
- Cleft irisC0266551
- Coloboma of irisC0266551
- Congenital coloboma of irisC0266551
- Congenital coloboma of iris (disorder)C0266551
- Iris colobomaC0266551
- Notched irisC0266551
- coloboma iridisC0266551
- coloboma irisC0266551
- coloboma of irisC0266551
- iris colobomaC0266551
- iris notchC0266551
Frequently Asked Questions
What is the ICD-10 code for coloboma of iris?
The ICD-10-CM code for coloboma of iris is Q13.0. The full clinical description is "Coloboma of iris". Q13.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q13.0 mean?
ICD-10-CM code Q13.0 represents "Coloboma of iris". 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 Q13.0 a billable code?
Yes, Q13.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q13.0 in?
Q13.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q13.0 map to?
Q13.0 maps to 36 SNOMED CT concepts: 718574003, 722282008, 248311001, 278530008, 724139004, and 31 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q13.0?
Q13.0 is linked to 2 UMLS Concept Unique Identifiers: C0009363, C0266551. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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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.