2026 ICD-10-CM Diagnosis Code Q10.0Congenital ptosis

ICD-10-CM CodesQ00-Q99Q10-Q18Q10

ICD-10-CM Q10.0
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

Q10.0 is a billable ICD-10-CM diagnosis code for congenital ptosis. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 124 through 125. The code is exempt from POA reporting. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Congenital malformations of eye, ear, face, neck.

Code Identity

ICD-10-CM Code
Q10.0
Billable Status
Yes — Valid for Submission
Code Describes
Congenital ptosis
Short Description
Congenital ptosis
Same as the full description in the CMS dataset.
Parent Code
Congenital malformations of eyelid, lacrimal apparatus and orbit

Code Classification

ChapterQ00-Q99Congenital malformations, deformations and chromosomal abnormalities
SectionQ10-Q18Congenital malformations of eye, ear, face and neck
CategoryQ10Congenital malformations of eyelid, lacrimal apparatus and orbit
This CodeQ10.0Congenital ptosis

Present on Admission (POA)Billing

Q10.0 is exempt from POA reporting on inpatient claims to general acute care hospitals. Review other POA exempt codes.

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Ablepharon
  • Aniridia, ptosis, intellectual disability, familial obesity syndrome
  • Bilateral congenital ptosis of upper eyelids
  • Bilateral ptosis of upper eyelids
  • Blepharophimosis epicanthus inversus ptosis syndrome
  • Blepharophimosis epicanthus inversus ptosis syndrome plus
  • Blepharophimosis, intellectual disability syndrome
  • Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome
  • Blepharoptosis, myopia, ectopia lentis syndrome
  • Conductive deafness, ptosis, skeletal anomalies syndrome
  • Congenital absence of lacrimal drainage structure
  • Congenital aniridia
  • Congenital dysgenetic ptosis
  • Congenital ectopic lens
  • Congenital ectopic pupil
  • Congenital myogenic ptosis
  • Congenital ptosis of left upper eyelid
  • Congenital ptosis of right upper eyelid
  • Congenital ptosis of upper eyelid
  • Deletion of part of long arm of chromosome 3
  • Dysgenesis of lacrimal punctum
  • Ectopic pupil
  • Epicanthal fold
  • Epicanthus inversus
  • Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth
  • Lower lacrimal punctum finding
  • Metopic ridging, ptosis, facial dysmorphism syndrome
  • Microbrachycephaly, ptosis, cleft lip syndrome
  • Myogenic ptosis
  • Partial ablepharon
  • Posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome
  • Ptosis and vocal cord paralysis syndrome
  • Ptosis, strabismus, ectopic pupil syndrome
  • Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome
  • Vagus nerve laryngeal paralysis

Index to Diseases and InjuriesGuidance

Alphabetical index entries that point to this code.

External Cause of Injuries IndexGuidance

References for this code in the External Cause of Injuries Index.

    • Anomaly, anomalous(congenital) (unspecified type)
      • eye
        • ptosis (eyelid)
    • Anomaly, anomalous(congenital) (unspecified type)
      • eyelid
        • ptosis
    • Blepharochalasis
      • congenital
    • Blepharoptosis
      • congenital
    • Ptosis
      • congenital (eyelid)
    • Ptosis
      • eyelid
        • congenital

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR MAL005
Congenital malformations of eye, ear, face, neck
Default principal diagnosis: inpatient Yes · outpatient Yes

Clinical InformationClinical

  • Congenital Ectopic Lens

    displacement of the lens of the eye secondary to defective zonule formation that is present at the time of birth.

Patient EducationClinical

Birth Defects

A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.

The full article covers:

  • What are birth defects?
  • What causes birth defects?
  • Who is at risk of having a baby with birth defects?
  • How are birth defects diagnosed?
  • What are the treatments for birth defects?
  • Can birth defects be prevented?

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Convert Q10.0 to ICD-9-CMHistory

The closest ICD-9-CM equivalents under the General Equivalence Mappings.

ICD-9-CM
743.61 Congenital ptosis
Exact Match The mapping is direct, with no qualifiers.

Code HistoryHistory

FY 2016AddedAdded to the ICD-10-CM code setEffective October 1, 2015, the first year of ICD-10-CM.
FY 2017–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About Q10.0Overview

Is Q10.0 a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report congenital ptosis on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What MS-DRG does Q10.0 group to?

When congenital ptosis is the principal diagnosis on an inpatient stay, it groups to MS-DRG 124, 125, with relative weights from 0.7678 to 1.3231 depending on complications. Higher weights mean higher Medicare reimbursement.

Is Q10.0 exempt from POA reporting?

Yes. CMS lists this code among those exempt from present on admission reporting, so hospitals do not assign a POA indicator for congenital ptosis on inpatient claims.

What is the ICD-9 equivalent of Q10.0?

Under the General Equivalence Mappings, congenital ptosis converts to ICD-9-CM 743.61 (congenital ptosis). The mapping is a direct match.

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.