Diagnosis Code: Q10.3

Short Description: Other congenital malformations of eyelid

Long Description: Other congenital malformations of eyelid

The code Q10.3 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations of eye, ear, face and neck (Q10-Q18)
    • Congenital malform of eyelid, lacrimal apparatus and orbit (Q10)
      • Q10.3 Other congenital malformations of eyelid

Code Version: 2022 ICD-10-CM

Synonyms

• Ablepharon
• Ablepharon
• Ablepharon
• Ablepharon macrostomia syndrome
• Ablepharon of bilateral eyelids
• Abnormal retraction of bilateral eyelids
• Abnormal retraction of left eyelid
• Abnormal retraction of right eyelid
• Absence of meibomian glands
• Accessory eyelid
• Accessory skeletal muscle
• Accessory skeletal muscle
• Agenesis of cilia of eyelid
• Anal atresia
• Anal atresia
• Ankyloblepharon
• Ankyloblepharon
• Ankyloblepharon
• Ankyloblepharon
• Ankyloblepharon
• Ankyloblepharon filiforme adnatum
• Ankyloblepharon filiforme adnatum
• Ankyloblepharon filiforme adnatum
• Ankyloblepharon filiforme adnatum with cleft palate syndrome
• Ankyloblepharon filiforme adnatum with imperforate anus syndrome
• Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome
• Bilateral coloboma of eyelid
• Bilateral congenital blepharophimosis of eyelids
• Bilateral congenital distichiasis
• Bilateral congenital symblepharon
• Bilateral epiblepharon
• Bilateral euryblepharon
• Bilateral symblepharon of eyes
• Blepharophimosis epicanthus inversus ptosis syndrome
• Blepharophimosis epicanthus inversus ptosis syndrome plus
• Blepharophimosis, intellectual disability syndrome
• Blepharophimosis, intellectual disability syndrome
• Blepharophimosis, intellectual disability syndrome
• Blepharophimosis, intellectual disability syndrome, Verloes type
• Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome
• Broad epicanthus
• Chorioretinal atrophy
• Coloboma of eyelid
• Coloboma of eyelid
• Coloboma of inferior eyelid
• Coloboma of superior eyelid
• Complete ablepharon
• Congenital abnormal retraction of bilateral eyelids
• Congenital abnormal retraction of eyelid
• Congenital abnormal shape of tarsal bone
• Congenital absence of eyelash
• Congenital absence of eyelash
• Congenital ankyloblepharon
• Congenital ankyloblepharon
• Congenital ankyloblepharon
• Congenital ankyloblepharon
• Congenital anomalies of eyelid, lacrimal system and orbit
• Congenital anomaly of eyelid
• Congenital anomaly of left eyelid
• Congenital anomaly of right eyelid
• Congenital blepharophimosis
• Congenital blepharophimosis
• Congenital blepharophimosis
• Congenital blepharophimosis
• Congenital blepharophimosis
• Congenital blepharophimosis
• Congenital blepharophimosis
• Congenital blepharophimosis
• Congenital cleft nose
• Congenital coloboma of left eyelid
• Congenital coloboma of right eyelid
• Congenital distichiasis
• Congenital distichiasis of left eyelid
• Congenital distichiasis of right eyelid
• Congenital epiblepharon-inferior oblique syndrome
• Congenital hypoplasia of nose
• Congenital macrostomia
• Congenital malposition of eyelid
• Congenital pes cavus
• Congenital scleral show
• Congenital tarsal kink
• Congenital vascular anomaly of eyelid
• Congenital vascular anomaly of lower eyelid
• Congenital vascular anomaly of upper eyelid
• Curly hair, ankyloblepharon, nail dysplasia syndrome
• Deletion of part of long arm of chromosome 3
• Distichiasis
• Dystopia canthorum
• Ectopic cilia of eyelid
• Epiblepharon
• Epiblepharon of left eye
• Epiblepharon of right eye
• Epicanthus finding
• Epicanthus finding
• Epicanthus finding
• Epicanthus finding
• Epicanthus finding
• Epicanthus finding
• Epicanthus inversus
• Epicanthus inversus
• Epicanthus inversus
• Epicanthus palpebralis
• Epicanthus tarsalis
• Euryblepharon
• Eyelid malposition
• Familial isolated trichomegaly
• Hypertelorism
• Hypertelorism
• Hypoplasia and coloboma of alar cartilage with telecanthus syndrome
• Hypoplasia of eyelid
• Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
• Isolated distichiasis
• Longitudinal deficiency of tarsal bone
• Macropalpebral fissure
• Mandibulofacial dysostosis, macroblepharon, macrostomia syndrome
• Microblepharia
• Microcornea
• Microcornea, myopic chorioretinal atrophy, telecanthus syndrome
• Microphthalmia with ankyloblepharon and intellectual disability syndrome
• Multiple supernumerary eye muscles
• Nasopalpebral lipoma coloboma syndrome
• Partial ablepharon
• Partial ablepharon
• Scleral show
• Short tarsus with absence of lower eyelashes syndrome
• Sphenoidal dysostosis
• STAR syndrome
• Supernumerary eye muscle
• Symblepharon
• Symblepharon of left eye
• Symblepharon of right eye
• Telecanthus
• Telecanthus
• Telecanthus
• Telecanthus, hypertelorism, strabismus, pes cavus syndrome
• X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome

Diagnostic Related Group(s)

The code Q10.3 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Disorders Of The Eye With Mcc Or Thrombolytic Agent (124)
• Other Disorders Of The Eye Without Mcc (125)

References to Index of Diseases and Injuries

The code Q10.3 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • 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

Crosswalk Information

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This page was last updated on: 10/1/2023

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