Q11.2
BillableMicrophthalmos
Microphthalmos
Status
Billable / Specific
Parent Code
Q11Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Cryptophthalmos NOS
- Dysplasia of eye
- Hypoplasia of eye
- Rudimentary eye
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- cryptophthalmos syndrome (Q87.0)
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
- Dysplasia of eye18821006
- Drusen of optic disc33629003
- Hyaline bodies of optic disc33629003
- Optic disc drusen33629003
- Optic nerve head drusen33629003
- Akinesia33994004
- Congenital small ears35045004
- Microtia35045004
- Agenesis of lens35387008
- Congenital absence of lens35387008
- Congenital aphakia35387008
- Globe of eye small61142002
- Microphthalmia61142002
- Microphthalmos61142002
- Small eyeball61142002
- Big jaw72855002
- Congenital prognathism72855002
- Exognathia72855002
- Progenia72855002
- Prognathia72855002
- Prognathism72855002
- Hypoplasia of eye86527000
- Rudimentary eye86527000
- Frontonasal dysplasia sequence86610004
- Median cleft face syndrome86610004
- Congenital hypoplasia of nose93278002
- Congenital hypoplastic nose93278002
- Congenital small nose93278002
- Congenital blindness95486002
- Congenital deafness95828007
- Ankyloblepharon193953008
- Nanophthalmos204108000
- Simple microphthalmos204108000
- Android fat distribution248311001
- Central obesity248311001
- Centripetal obesity248311001
- Fat body with thin limbs248311001
- Obesity of face and trunk, sparing limbs248311001
- Truncal obesity248311001
- Ankyloblepharon totale253213006
- Blepharosynechia253213006
- Congenital ankyloblepharon253213006
- Fused eyelids253213006
- Cryptophthalmia400951005
- Cryptophthalmos400951005
- Lenz microphthalmia syndrome438504004
- MMEP syndrome715533002
- Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome715533002
- Syndromic microphthalmia type 8715533002
- Viljoen Smart syndrome715533002
- Colobomatous microphthalmia715771008
- Microphthalmia with colobomatous cyst715771008
- Microphthalmos co-occurrent with congenital ocular coloboma715771008
- Nanophthalmia716775009
- Microphthalmia with ankyloblepharon and intellectual disability syndrome717222003
- Syndromic microphthalmia type 4717222003
- Isolated cryptophthalmia718691008
- Isolated cryptophthalmos718691008
- Syndromic microphthalmia due to OTX2 mutation718761007
- Syndromic microphthalmia due to orthodenticle homeobox 2 mutation718761007
- Syndromic microphthalmia type 5718761007
- MOBA syndrome720010009
- Microphthalmia with brain atrophy syndrome720010009
- Syndromic microphthalmia type 10720010009
- Bakrania Ragge syndrome721878003
- Microphthalmia with brain and digit anomaly721878003
- Syndromic microphthalmia type 6721878003
- MIDAS syndrome721879006
- MIDAS syndrome (microphthalmia, dermal aplasia, sclerocornea) syndrome721879006
- Microphthalmia with linear skin defect syndrome721879006
- Syndromic microphthalmia type 7721879006
- Mackay Shek Carr syndrome723503006
- Retinal degeneration, nanophthalmos, glaucoma syndrome723503006
- Bosma Henkin Christiansen syndrome724281002
- Bosma arhinia microphthalmia syndrome724281002
- Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome724281002
- Microphthalmic socket762414004
- Colobomatous microphthalmia, rhizomelic dysplasia syndrome764942005
- Microphthalmia, coloboma, rhizomelic skeletal dysplasia764942005
- X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome771148008
- X-linked colobomatous microphthalmia, microcephaly, short stature, psychomotor retardation syndrome771148008
- Macrosomia, microphthalmia, cleft palate syndrome773282001
- Teebi Al Saleh Hassoon syndrome773282001
- ALX1 (aristaless-like homeobox 1) related frontonasal dysplasia773628009
- ALX1-related frontonasal dysplasia773628009
- Frontonasal dysplasia type 3773628009
- Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome773628009
- Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome776204008
- Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome778021002
- Nanophthalmos, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome778021002
- 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
- Bilateral partial cryptophthalmos890362008
- Partial cryptophthalmos of bilateral eyelids890362008
- Partial cryptophthalmos of both eyelids890362008
- Complete cryptophthalmia890406007
- Complete cryptophthalmos890406007
- Bilateral cryptophthalmia890414001
- Bilateral cryptophthalmos890414001
- Congenital cryptophthalmos of bilateral eyelids890414001
- Congenital cryptophthalmos of both eyelids890414001
- Microphthalmos due to Delleman syndrome1003369001
- Microphthalmos due to Fryns syndrome1003370000
- Microphthalmos due to branchio-oculo-facial syndrome1003372008
- Microphthalmia, microtia, fetal akinesia syndrome1230344000
- Microphthalmia, microtia, foetal akinesia syndrome1230344000
- Thomas Jewett Raines syndrome1230344000
- Syndromic nanophthalmos due to Kenny-Caffey syndrome1231626009
- Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome1303582008
- 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
- Microphthalmia of left eye15987231000119104
- Microphthalmos of left eye15987231000119104
- Microphthalmia of right eye15987191000119108
- Microphthalmos of right eye15987191000119108
UMLS
- Congenital microphthalmosC0026010
- Globe of eye smallC0026010
- MicrophthalmiaC0026010
- MicrophthalmosC0026010
- Microphthalmos (disorder)C0026010
- Microphthalmos, unspecifiedC0026010
- NanophthalmosC0026010
- Simple microphthalmosC0026010
- Simple microphthalmos (disorder)C0026010
- Small eyeballC0026010
- congenital microphthalmosC0026010
- microphthalmiaC0026010
- microphthalmosC0026010
- nanophthalmosC0026010
- CryptophthalmiaC0311249
- CryptophthalmosC0311249
- Cryptophthalmos (disorder)C0311249
- Cryptophthalmos NOSC0311249
- cryptophthalmiaC0311249
- cryptophthalmosC0311249
- Dysplasia of eyeC0266524
- Dysplasia of eye (disorder)C0266524
- Hypoplasia of eyeC0266527
- Hypoplasia of eye (disorder)C0266527
- Rudimentary eyeC0266527
Frequently Asked Questions
What is the ICD-10 code for microphthalmos?
The ICD-10-CM code for microphthalmos is Q11.2. The full clinical description is "Microphthalmos". Q11.2 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q11.2 mean?
ICD-10-CM code Q11.2 represents "Microphthalmos". 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 Q11.2 a billable code?
Yes, Q11.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q11.2 in?
Q11.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q11.2?
Q11.2 has Excludes1 notes indicating codes that cannot be used together with it, including: cryptophthalmos syndrome (Q87.0).
What SNOMED CT codes does Q11.2 map to?
Q11.2 maps to 51 SNOMED CT concepts: 773628009, 35387008, 33994004, 248311001, 193953008, and 46 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q11.2?
Q11.2 is linked to 4 UMLS Concept Unique Identifiers: C0026010, C0311249, C0266524, C0266527. 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.