2026 ICD-10-CM Diagnosis Code Q12.4Spherophakia
ICD-10-CM Codes›Q00-Q99›Q10-Q18›Q12
- Billable — Valid for Submission
- POA Exempt
- Chronic Condition
Q12.4 is a billable ICD-10-CM diagnosis code for spherophakia. 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
Code Classification
Present on Admission (POA)Billing
Q12.4 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.
- Bilateral spherophakia
- GEMSS syndrome
- Ichthyosis, short stature, brachydactyly, microspherophakia syndrome
- Isolated microspherophakia
- Lentiglobus
- Megalocornea
- Megalocornea, spherophakia, secondary glaucoma syndrome
- Microphakia
- Microspherophakia
- Microspherophakia with metaphyseal dysplasia syndrome
- Spherophakia
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- sphericity, lens - Q12.4
- Sphericity, increased, lens (congenital) - Q12.4
- Spherophakia - Q12.4
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Increase, increased
- sphericity, lens
- Sphericity, increased, lens(congenital)
- Spherophakia
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Spherophakia
a congenital disorder of the eye where the lens is abnormally small and spherical.Weill-Marchesani Syndrome 1|Congenital Mesodermal Dysmorphodystrophy|Spherophakia-Brachymorphia Syndrome|Spherophakia-brachymorphia syndrome|Weill-Marchesani, Autosomal Recessive
an autosomal recessive subtype of weill-marchesani syndrome caused by mutations in the adamts10 gene, encoding a disintegrin and metalloproteinase with thrombospondin motifs 10.
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 Q12.4 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About Q12.4Overview
Is Q12.4 (Congenital lens malformations) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report spherophakia on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does Q12.4 group to?
When spherophakia 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 Q12.4 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 spherophakia on inpatient claims.
What is the ICD-9 equivalent of Q12.4?
Under the General Equivalence Mappings, spherophakia converts to ICD-9-CM 743.36 (anomalies of lens shape). The mapping is approximate, so confirm the match fits the documentation.
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.
