Eyelid malformation, congenital NOS
Lopes Gorlin syndrome
Absence of meibomian glands
Congenital structural abnormality of eyelid (disorder)
CHANDS - Curly hair, ankyloblepharon, nail dysplasia syndrome
Congenital abnormality of eyelid
Aughton Hufnagle syndrome
Hypoplasia and coloboma of alar cartilage with telecanthus syndrome
Epicanthal fold of both eyes
Houlston Ironton Temple syndrome
Ankyloblepharon
Isolated congenital distichiasis
Distichiasis of left eyelid
Congenital macrostomia
Microphthalmia with ankyloblepharon and intellectual disability syndrome
Epicanthic fold
Orbital separation excessive
Congenital blepharophimosis of left eyelid
Epiblepharon of right eye
Congenital blepharophimosis of bilateral eyelids
Congenital misshapen tarsal bone
Microblepharism
Left symblepharon
Broad epicanthus of left eye
Blepharosynechia
Syndactyly, telecanthus, anogenital and renal malformation syndrome
Short tarsus with absence of lower eyelashes syndrome
Atresia ani
Coloboma of lid
Congenital abnormal retraction of eyelid
Cornea small
Euryblepharon of bilateral eyelids
Ablepharon (absent eyelids)
Full thickness defect of the eyelid
Bilateral congenital symblepharon
Symblepharon
Scleral show
Aproctia
Blepharophimosis epicanthus inversus ptosis syndrome
Chorioretinal atrophy
Microcornea
Absent eyelids
Curly hair, ankyloblepharon, nail dysplasia syndrome
Eyelid colobomata
Eyelid coloboma
Ankyloblepharon filiforme adnatum with imperforate anus syndrome
Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome
Congenital hypoplasia of nose
Congenital structural abnormality of left eyelid
Congenital small nose
Congenital malformation of eyelid
Congenital coloboma of bilateral eyelids
Accessory eye muscles
Congenital symblepharon of both conjunctivae
Epicanthal fold of right eye
Longitudinal deficiency of tarsal bone
Complete ablepharon (disorder)
Congenital absence or agenesis of cilia
Coloboma of eyelid (disorder)
Congenital distichiasis of both eyelashes
Cleft eyelid
Congenital distichiasis of bilateral eyelids
Agenesis of cilia
Broad epicanthus
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome
Agenesis of eyelids
Notched eyelids
Congenital coloboma of right eyelid
Developmental anomaly of eyelid
Congenital absence or agenesis of eyelid
Ohdo blepharophimosis syndrome
Eyes wide apart
Ankyloblepharon totale
Frydman Cohen Karmon syndrome
Bilateral euryblepharon
Coloboma palpebrale
Partial ablepharon
Macroblepharon, ectropion, hypertelorism, macrostomia syndrome
Bilateral ablepharon
STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome
Blepharophimosis, intellectual disability syndrome, Verloes type
Nasopalpebral lipoma coloboma syndrome
Epiblepharon
Palpebral coloboma
Congenital malformation of eyelid NOS
Bilateral symblepharon
Hypoplasia of eyelid
Accessory skeletal muscle
Coloboma of eyelid
Congenital symblepharon of bilateral conjunctivae
ablepharon
Congenital absence of eyelid
Epicanthal fold of bilateral eyes
Open eye
STAR syndrome
Mental retardation, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
Supernumerary eye muscle
Deletion of part of long arm of chromosome 3
Pathological lid adhesions
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2-related blepharophimosis, intellectual disability syndrome
Blepharophimosis congenital
Congenital anomalies of eyelid, lacrimal system and orbit
Notched eyelid
Broad epicanthus of bilateral eyes
Atretoblepharia
BPES (blepharophimosis epicanthus inversus ptosis syndrome) plus
Congenital anomaly of eyelid
Congenital blepharophimosis of both eyelids
Accessory eye muscle
Congenital coloboma of left eyelid
Congenital tarsal kink
Blepharophimosis epicanthus inversus ptosis syndrome plus
Congenital vascular anomaly of eyelid
Congenital scleral show
Congenital atresia of anus
Symblepharon of bilateral eyes
Congenital blepharophimosis of right palpebral fissure
Accessory muscle
Orbital hypertelorism
Epicanthus palpebralis
Congenital structural abnormality of eyelid
Epicanthus tarsalis
Bilateral symblepharon of eyes
Ankyloblepharon filiforme adnatum
Complete ablepharon
3q23 microdeletion syndrome
Eyes widely set
Microblephary
Coloboma of the Eyelid
Distichiasis of right eyelid
Congenital blepharophimosis (disorder)
Right symblepharon
SMARCA2-related blepharophimosis, intellectual disability syndrome
Missing eyelids
Alar cartilage hypoplasia, coloboma, telecanthus syndrome
eyes open
Telecanthus
Epicanthal fold
Congenital anomaly of left eyelid
Congenital Eyelid Malformation
Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
Congenital absence of cilia of eyelid
Congenital abnormal shape of tarsal bone
coloboma palpebral
Bilateral epiblepharon
Imperforate anus
Abnormal retraction of bilateral eyelids
Absence of eyelashes
Congenital hypoplastic nose
Congenital pes cavus
Epicanthal fold of left eye
Congenital accessory eye muscle
Congenital cleft nose
Congenital distichiasis of right eyelid
Eyelid malposition
Blepharophimosis, intellectual disability syndrome type V
Hypertelorism
BPES - blepharophimosis epicanthus inversus ptosis syndrome
Ablepharon - absent eyelids
Symblepharon of left eye
Dystopia canthorum
SMARCA2 (SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 2) related blepharophimosis, intellectual disability syndrome
Congenital structural abnormality of bilateral eyelids
Macrostomia
Telecanthus, hypertelorism, strabismus, pes cavus syndrome
Inferior palpebral coloboma
Reduplication of lashes
Familial isolated trichomegaly
Congenital epiblepharon-inferior oblique syndrome
agenesis eyelid
lid coloboma
Congenital accessory eyelid
Congenital distichiasis
Bilateral congenital blepharophimosis of eyelids
Ablepharia
Agenesis of eyelid
Multiple supernumerary eye muscles
Congenital blepharophimosis of right eyelid
Congenital distichiasis of bilateral eyelashes
Abnormal retraction of right eyelid
Agenesis of cilia of eyelid
Coloboma of lower eyelid
Euryblepharon
Coloboma of superior eyelid
Congenital imperforate anus
Isolated distichiasis
Epicanthus inversus
Macropalpebral fissure
Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome
Congenital ankyloblepharon
Fused eyelids
MMCAT (microcornea, myopic chorioretinal atrophy, telecanthus) syndrome
Epiblepharon of bilateral eyelids
Broad epicanthus of right eye
Congenital abnormal retraction of bilateral eyelids
Mandibulofacial dysostosis, macroblepharon, macrostomia syndrome
Blepharophimosis, intellectual disability syndrome
Congenital cavus foot
Ectopic cilia of eyelid
Microblepharia
Bilateral broad epicanthi
Sphenoidal dysostosis
Blepharophimosis, congenital
Lid Gap
Ablepharon macrostomia syndrome
Congenital vascular anomaly of upper eyelid
Congenital anomaly of right eyelid
Congenital malposition of eyelid
Abnormal retraction of left eyelid
Distichiasis
Superior palpebral coloboma
Syndromic microphthalmia type 4
Congenital structural abnormality of right eyelid
Symblepharon of both eyes
Congenital distichiasis of left eyelid
Bilateral congenital distichiasis
Congenital notching of palpebral fissure
Anal atresia
MMCAT syndrome
Eyelid disorders congenital
Broad epicanthus of both eyes
Ablepharon of bilateral eyelids
Multiple accessory eye muscles
Bilateral epicanthal folds
Ankyloblepharon filiforme adnatum with cleft palate syndrome
Congenital eyelid deformity
Coloboma of upper eyelid
Ablepharon of eyelid
Accessory eyelid
Congenital blepharophimosis of left palpebral fissure
X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome
Congenital eyelid malformation NOS
Eyelid colobomas
Epiblepharon of left eye
Congenital absence of eyelash
Coloboma of inferior eyelid
Ablepharon (disorder)
Congenital blepharophimosis
Cleft nose
Congenital vascular anomaly of lower eyelid
Symblepharon of right eye
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome

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.

How does Q10.3 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other congenital malformations of eyelid 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 Q10.3?

Q10.3 maps to the ICD-11 code: LA14.Z (Structural developmental anomalies of eyelid, lacrimal apparatus or orbit, 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.