Q10.3
Other congenital malformations of eyelid
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
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
cleft lip and cleft palate (Q35-Q37) congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4) congenital malformation of larynx (Q31.-) congenital malformation of lip NEC (Q38.0) congenital malformation of nose (Q30.-) congenital malformation of parathyroid gland (Q89.2) congenital malformation of thyroid gland (Q89.2)
inborn errors of metabolism (E70-E88)
Official Guidelines for Q10.3
FY 2026 ›Sections that reference Q10.3
Sections whose FY 2026 text names Q10.3, its Q10 category, or a range containing it — the chapter guidance above is the authoritative source.
Find Q10.3 in the alphabetic index
25 index paths lead to this code
- Ablepharia, ablepharon
- Epiblepharon
- Epicanthus, epicanthic fold
- Narrowness, abnormal, eyelid
- Absence › cilia
- Absence › eyelid
- Accessory › eye muscle
- Accessory › eyelid
- Agenesis › cilia
- Agenesis › eyelid
- Ankyloblepharon › filiforme
- Ankyloblepharon › total
- Anomaly, anomalous › canthus
- Anomaly, anomalous › cilia
- Anomaly, anomalous › eyelid
- Anomaly, anomalous › lid
- Anomaly, anomalous › narrowness, eyelid
- Atrophy, atrophic › tarso-orbital fascia, congenital
- Blepharophimosis › congenital
- Coloboma › eyelid
- Deformity › ocular muscle
- Fold, folds › epicanthic
- Hypoplasia, hypoplastic › eyelid
- Insufficiency, insufficient › tarso-orbital fascia, congenital
- Symblepharon › congenital