Q10.3
BillableOther congenital malformations of eyelid
Other congenital malformations of eyelid
Status
Billable / Specific
Parent Code
Q10Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Ablepharon
- Blepharophimosis, congenital
- Coloboma of eyelid
- Congenital absence or agenesis of cilia
- Congenital absence or agenesis of eyelid
- Congenital accessory eyelid
- Congenital accessory eye muscle
- Congenital malformation of eyelid NOS
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
- Ablepharia13401001
- Ablepharon13401001
- Ablepharon - absent eyelids13401001
- Open eye13401001
- Eyes wide apart22006008
- Eyes widely set22006008
- Hypertelorism22006008
- Orbital hypertelorism22006008
- Orbital separation excessive22006008
- Accessory eyelid24606006
- Cornea small26098002
- Microcornea26098002
- Longitudinal deficiency of tarsal bone29581008
- Congenital macrostomia40159009
- Macrostomia40159009
- Partial ablepharon45484000
- Accessory muscle50847000
- Accessory skeletal muscle50847000
- Congenital absence of cilia of eyelid63935007
- Congenital absence of eyelash63935007
- Accessory eye muscle85697009
- Supernumerary eye muscle85697009
- Atretoblepharia90216006
- Pathological lid adhesions90216006
- Symblepharon90216006
- Congenital abnormality of eyelid91158006
- Congenital anomaly of eyelid91158006
- Congenital eyelid deformity91158006
- Congenital malformation of eyelid91158006
- Congenital structural abnormality of eyelid91158006
- Developmental anomaly of eyelid91158006
- Congenital abnormal shape of tarsal bone92951004
- Congenital misshapen tarsal bone92951004
- Congenital blepharophimosis93040009
- Congenital hypoplasia of nose93278002
- Congenital hypoplastic nose93278002
- Congenital small nose93278002
- Microblepharia94684003
- Microblepharism94684003
- Microblephary94684003
- Coloboma of eyelid95202004
- Coloboma of lid95202004
- Coloboma palpebrale95202004
- Congenital notching of palpebral fissure95202004
- Eyelid coloboma95202004
- Palpebral coloboma95202004
- Distichiasis95339000
- Reduplication of lashes95339000
- Macropalpebral fissure95503005
- Ectopic cilia of eyelid95504004
- Chorioretinal atrophy95686007
- Sphenoidal dysostosis109414004
- Ankyloblepharon193953008
- Congenital anomalies of eyelid, lacrimal system and orbit204196008
- Hypoplasia of eyelid204203001
- Accessory eye muscles204216001
- Multiple accessory eye muscles204216001
- Multiple supernumerary eye muscles204216001
- Cleft nose204521002
- Congenital cleft nose204521002
- Anal atresia204712000
- Aproctia204712000
- Atresia ani204712000
- Congenital atresia of anus204712000
- Congenital imperforate anus204712000
- Imperforate anus204712000
- Congenital cavus foot205091006
- Congenital pes cavus205091006
- CHANDS - Curly hair, ankyloblepharon, nail dysplasia syndrome239037001
- Curly hair, ankyloblepharon, nail dysplasia syndrome239037001
- Telecanthus246803005
- Absence of meibomian glands246836006
- Epiblepharon253212001
- Ankyloblepharon totale253213006
- Blepharosynechia253213006
- Congenital ankyloblepharon253213006
- Fused eyelids253213006
- Congenital distichiasis253214000
- Congenital epiblepharon-inferior oblique syndrome360429003
- Ankyloblepharon filiforme adnatum400952003
- Congenital tarsal kink400953008
- Euryblepharon400954002
- Epicanthus tarsalis400955001
- Epicanthus inversus400956000
- Epicanthus palpebralis400957009
- Eyelid malposition404625000
- Broad epicanthus407552008
- Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth412787009
- Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth412787009
- Ohdo blepharophimosis syndrome412787009
- Scleral show424033007
- Congenital scleral show444668001
- Congenital vascular anomaly of eyelid700278007
- Congenital vascular anomaly of upper eyelid700279004
- Congenital vascular anomaly of lower eyelid700369004
- Agenesis of eyelid708541009
- Complete ablepharon708541009
- Congenital absence of eyelid708541009
- BPES - blepharophimosis epicanthus inversus ptosis syndrome715391004
- Blepharophimosis epicanthus inversus ptosis syndrome715391004
- Congenital abnormal retraction of eyelid715769008
- Microphthalmia with ankyloblepharon and intellectual disability syndrome717222003
- Syndromic microphthalmia type 4717222003
- Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome717914000
- Frydman Cohen Karmon syndrome717914000
- Ablepharon macrostomia syndrome718575002
- X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome718896000
- Lopes Gorlin syndrome721075001
- Short tarsus with absence of lower eyelashes syndrome721075001
- Alar cartilage hypoplasia, coloboma, telecanthus syndrome722284009
- Hypoplasia and coloboma of alar cartilage with telecanthus syndrome722284009
- Nasopalpebral lipoma coloboma syndrome723411003
- STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome723581006
- STAR syndrome723581006
- Syndactyly, telecanthus, anogenital and renal malformation syndrome723581006
- Deletion of part of long arm of chromosome 3726370000
- Congenital malposition of eyelid726406009
- Dystopia canthorum726407000
- Telecanthus, hypertelorism, strabismus, pes cavus syndrome733067006
- Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome763066009
- Houlston Ironton Temple syndrome763066009
- Coloboma of superior eyelid763132003
- Coloboma of upper eyelid763132003
- Superior palpebral coloboma763132003
- Coloboma of inferior eyelid763133008
- Coloboma of lower eyelid763133008
- Inferior palpebral coloboma763133008
- Familial isolated trichomegaly764523004
- Macroblepharon, ectropion, hypertelorism, macrostomia syndrome773557002
- Mandibulofacial dysostosis, macroblepharon, macrostomia syndrome773557002
- Ankyloblepharon filiforme adnatum with imperforate anus syndrome773770009
- Aughton Hufnagle syndrome773770009
- MMCAT (microcornea, myopic chorioretinal atrophy, telecanthus) syndrome774212003
- MMCAT syndrome774212003
- Microcornea, myopic chorioretinal atrophy, telecanthus syndrome774212003
- Blepharophimosis, intellectual disability syndrome type V778009001
- Blepharophimosis, intellectual disability syndrome, Verloes type778009001
- Ankyloblepharon filiforme adnatum with cleft palate syndrome783204009
- Blepharophimosis, intellectual disability syndrome788584007
- Ablepharon of bilateral eyelids838334004
- Bilateral ablepharon838334004
- Bilateral congenital distichiasis840478008
- Congenital distichiasis of bilateral eyelashes840478008
- Congenital distichiasis of bilateral eyelids840478008
- Congenital distichiasis of both eyelashes840478008
- Congenital abnormal retraction of bilateral eyelids840486008
- 3q23 microdeletion syndrome890180006
- BPES (blepharophimosis epicanthus inversus ptosis syndrome) plus890180006
- Blepharophimosis epicanthus inversus ptosis syndrome plus890180006
- Bilateral epiblepharon890348001
- Epiblepharon of bilateral eyelids890348001
- Bilateral euryblepharon890349009
- Euryblepharon of bilateral eyelids890349009
- Congenital coloboma of bilateral eyelids890417008
- Bilateral congenital symblepharon890461000
- Congenital symblepharon of bilateral conjunctivae890461000
- Congenital symblepharon of both conjunctivae890461000
- Agenesis of cilia1003553009
- Agenesis of cilia of eyelid1003553009
- Absence of eyelashes1145105002
- Isolated congenital distichiasis1263461006
- Isolated distichiasis1263461006
- SMARCA2 (SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2) related blepharophimosis, intellectual disability syndrome1300198006
- SMARCA2-related blepharophimosis, intellectual disability syndrome1300198006
- SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2-related blepharophimosis, intellectual disability syndrome1300198006
- Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome1304113005
- Epicanthal fold1362054007
- Epicanthic fold1362054007
- Broad epicanthus of right eye1366520004
- Broad epicanthus of left eye1366521000
- Bilateral broad epicanthi1366522007
- Broad epicanthus of bilateral eyes1366522007
- Broad epicanthus of both eyes1366522007
- Abnormal retraction of bilateral eyelids11718451000119104
- Abnormal retraction of left eyelid340751000119102
- Abnormal retraction of right eyelid335141000119105
- Bilateral congenital blepharophimosis of eyelids15980871000119104
- Congenital blepharophimosis of bilateral eyelids15980871000119104
- Congenital blepharophimosis of both eyelids15980871000119104
- Bilateral epicanthal folds16091531000119100
- Epicanthal fold of bilateral eyes16091531000119100
- Epicanthal fold of both eyes16091531000119100
- Bilateral symblepharon343301000119106
- Bilateral symblepharon of eyes343301000119106
- Symblepharon of bilateral eyes343301000119106
- Symblepharon of both eyes343301000119106
- Congenital anomaly of left eyelid15980791000119108
- Congenital structural abnormality of left eyelid15980791000119108
- Congenital anomaly of right eyelid15980831000119102
- Congenital structural abnormality of right eyelid15980831000119102
- Congenital blepharophimosis of left eyelid679951000119103
- Congenital blepharophimosis of left palpebral fissure679951000119103
- Congenital blepharophimosis of right eyelid679981000119105
- Congenital blepharophimosis of right palpebral fissure679981000119105
- Congenital coloboma of left eyelid15988031000119109
- Congenital coloboma of right eyelid15988071000119107
- Congenital distichiasis of left eyelid15937301000119106
- Distichiasis of left eyelid15937301000119106
- Congenital distichiasis of right eyelid15937341000119108
- Distichiasis of right eyelid15937341000119108
- Congenital structural abnormality of bilateral eyelids15980911000119101
- Epiblepharon of left eye15665161000119108
- Epiblepharon of right eye15665121000119103
- Epicanthal fold of left eye16091491000119100
- Epicanthal fold of right eye16091571000119102
- Left symblepharon337511000119106
- Symblepharon of left eye337511000119106
- Right symblepharon331891000119108
- Symblepharon of right eye331891000119108
UMLS
- AblephariaC0266574
- AblepharonC0266574
- Ablepharon (absent eyelids)C0266574
- Ablepharon (disorder)C0266574
- Ablepharon - absent eyelidsC0266574
- Ablepharon of eyelidC0266574
- Absent eyelidsC0266574
- Agenesis of eyelidC0266574
- Agenesis of eyelidsC0266574
- Complete ablepharonC0266574
- Complete ablepharon (disorder)C0266574
- Congenital absence of eyelidC0266574
- Lid GapC0266574
- Missing eyelidsC0266574
- Open EyeC0266574
- Open eyeC0266574
- ablepharonC0266574
- agenesis eyelidC0266574
- eyes openC0266574
- Blepharophimosis congenitalC0344502
- Blepharophimosis, congenitalC0344502
- Congenital blepharophimosisC0344502
- Congenital blepharophimosis (disorder)C0344502
- Cleft eyelidC0521573
- Coloboma of eyelidC0521573
- Coloboma of eyelid (disorder)C0521573
- Coloboma of lidC0521573
- Coloboma of the EyelidC0521573
- Coloboma palpebraleC0521573
- Congenital notching of palpebral fissureC0521573
- Eyelid colobomaC0521573
- Eyelid colobomasC0521573
- Eyelid colobomataC0521573
- Full thickness defect of the eyelidC0521573
- Lid colobomaC0521573
- Notched eyelidC0521573
- Notched eyelidsC0521573
- Palpebral colobomaC0521573
- coloboma palpebralC0521573
- eyelid colobomaC0521573
- lid colobomaC0521573
- Congenital Eyelid MalformationC0266572
- Congenital abnormality of eyelidC0266572
- Congenital anomaly of eyelidC0266572
- Congenital eyelid deformityC0266572
- Congenital eyelid malformationC0266572
- Congenital eyelid malformation NOSC0266572
- Congenital malformation of eyelidC0266572
- Congenital malformation of eyelid NOSC0266572
- Congenital structural abnormality of eyelidC0266572
- Congenital structural abnormality of eyelid (disorder)C0266572
- Developmental anomaly of eyelidC0266572
- Eyelid disorders congenitalC0266572
- Eyelid malformation, congenital NOSC0266572
- Congenital absence or agenesis of ciliaC2910111
- Congenital absence or agenesis of eyelidC2910112
- Congenital accessory eye muscleC2910113
- Congenital accessory eyelidC2910114
- Other congenital malformations of eyelidC0477978
Frequently Asked Questions
What is the ICD-10 code for other congenital malformations of eyelid?
The ICD-10-CM code for other congenital malformations of eyelid is Q10.3. The full clinical description is "Other congenital malformations of eyelid". Q10.3 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q10.3 mean?
ICD-10-CM code Q10.3 represents "Other congenital malformations of eyelid". 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 Q10.3 a billable code?
Yes, Q10.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q10.3 in?
Q10.3 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q10.3?
Q10.3 has Excludes1 notes indicating codes that cannot be used together with it, including: cryptophthalmos NOS (Q11.2); cryptophthalmos syndrome (Q87.0).
What SNOMED CT codes does Q10.3 map to?
Q10.3 maps to 113 SNOMED CT concepts: 890180006, 13401001, 718575002, 838334004, 11718451000119104, and 108 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q10.3?
Q10.3 is linked to 9 UMLS Concept Unique Identifiers: C0266574, C0344502, C0521573, C0266572, C2910111, and 4 more. 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.