2024 ICD-10-CM Diagnosis Code Q10.3

Other congenital malformations of eyelid

ICD-10-CM Code:
Q10.3
ICD-10 Code for:
Other congenital malformations of eyelid
Is Billable?
Yes - Valid for Submission
Chronic Condition Indicator: [1]
Chronic
Code Navigator:

Code Classification

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

Q10.3 is a billable diagnosis code used to specify a medical diagnosis of other congenital malformations of eyelid. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2023 through September 30, 2024. The code is exempt from present on admission (POA) reporting for inpatient admissions to general acute care hospitals.

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

  • 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

Clinical Classification

Clinical Information

  • Hypertelorism

    abnormal increase in the interorbital distance due to overdevelopment of the lesser wings of the sphenoid.
  • Microcornea

    a congenital abnormality characterized by an abnormally small cornea. the horizontal corneal diameter is less than 10mm or less than 9mm in newborns. it is associated with an increased risk of glaucoma.

Tabular List of Diseases and Injuries

The following annotation back-references are applicable to this diagnosis code. The Tabular List of Diseases and Injuries is a list of ICD-10-CM codes, organized "head to toe" into chapters and sections with coding notes and guidance for inclusions, exclusions, descriptions and more.


Inclusion Terms

Inclusion Terms
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
  • 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

Index to Diseases and Injuries References

The following annotation back-references for this diagnosis code are found in the injuries and diseases index. The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10-CM code(s).

Present on Admission (POA)

Q10.3 is exempt from POA reporting - The Present on Admission (POA) indicator is used for diagnosis codes included in claims involving inpatient admissions to general acute care hospitals. POA indicators must be reported to CMS on each claim to facilitate the grouping of diagnoses codes into the proper Diagnostic Related Groups (DRG). CMS publishes a listing of specific diagnosis codes that are exempt from the POA reporting requirement. Review other POA exempt codes here.

CMS POA Indicator Options and Definitions

POA IndicatorReason for CodeCMS will pay the CC/MCC DRG?
YDiagnosis was present at time of inpatient admission.YES
NDiagnosis was not present at time of inpatient admission.NO
UDocumentation insufficient to determine if the condition was present at the time of inpatient admission.NO
WClinically undetermined - unable to clinically determine whether the condition was present at the time of inpatient admission.YES
1Unreported/Not used - Exempt from POA reporting. NO

Convert Q10.3 to ICD-9-CM

  • ICD-9-CM Code: 743.62 - Congenital eyelid deform
    Approximate Flag - The approximate mapping means there is not an exact match between the ICD-10 and ICD-9 codes and the mapped code is not a precise representation of the original code.
  • ICD-9-CM Code: 743.63 - Spec anom of eyelid NEC
    Approximate Flag - The approximate mapping means there is not an exact match between the ICD-10 and ICD-9 codes and the mapped code is not a precise representation of the original code.
  • ICD-9-CM Code: 743.69 - Anom eyelid/lacr/orb NEC
    Approximate Flag - The approximate mapping means there is not an exact match between the ICD-10 and ICD-9 codes and the mapped code is not a precise representation of the original code.

Patient Education


Eyelid Disorders

Your eyelids help protect your eyes. When you blink, your eyelids spread moisture over your eyes. Blinking also helps move dirt or other particles off the surface of the eye. You close your eyelids when you see something coming toward your eyes. This can help protect against injuries.

Like most other parts of your body, your eyelids can get infected, inflamed, or even develop cancer. There are also specific eyelid problems, including:

  • Eyelids that turn in or out
  • Eyelids that droop
  • Abnormal blinking or twitching

Treatment of eyelid problems depends on the cause.


[Learn More in MedlinePlus]

Code History

  • FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
  • FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
  • FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
  • FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
  • FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
  • FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
  • FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
  • FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
  • FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016. This was the first year ICD-10-CM was implemented into the HIPAA code set.

Footnotes

[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:

  • The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
  • The condition places limitations on self-care, independent living, and social interactions.