InnovaRx Innova Health Strategies

Q10.3

Other congenital malformations of eyelid

Billable FY2026 2025-10-01 → 2026-09-30
Exclusions 9 never code together
Q10code
Excludes1
  • cryptophthalmos NOS (Q11.2)Q11.2
  • cryptophthalmos syndrome (Q87.0)Q87.0
Q10-Q18block
Excludes2
  • cleft lip and cleft palate (Q35-Q37)Q35-Q37
  • congenital malformation of cervical spine (Q05.0, Q05.5, Q67.5, Q76.0-Q76.4)Q05.0Q05.5Q67.5Q76.0-Q76.4
  • congenital malformation of larynx (Q31.-)Q31.-
  • congenital malformation of lip NEC (Q38.0)Q38.0
  • congenital malformation of nose (Q30.-)Q30.-
  • congenital malformation of parathyroid gland (Q89.2)Q89.2
  • congenital malformation of thyroid gland (Q89.2)Q89.2

Excludes1 — never code together. The excluded condition and this one are mutually exclusive.

Excludes2 — not included here, but the patient may have both. Code both when documented.

Instructional notes 8
Q10.3code
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
Index entries leading here 20
  • Ablepharia, ablepharon Q10.3
  • Absence (of) (organ or part) (complete or partial)
    • cilia (congenital) Q10.3
    • eyelid (fold) (congenital) Q10.3
    • muscle (congenital) (pectoral) Q79.8
    • eye (acquired) Z90.01
      • muscle (congenital) Q10.3
  • Accessory (congenital)
  • Agenesis
  • Ankyloblepharon (eyelid) (acquired) — see also Blepharophimosis
    • filiforme (adnatum) (congenital) Q10.3
    • total Q10.3
  • Anomaly, anomalous (congenital) (unspecified type) Q89.9
  • Atrophy, atrophic (of)
    • tarso-orbital fascia, congenital Q10.3
  • Blepharophimosis (eyelid) H02.529
  • Imperfect
    • closure (congenital)
  • Coloboma (iris) Q13.0
  • Symblepharon H11.23
  • Deformity Q89.9
    • eyelid (acquired) — see also Disorder, eyelid, specified type NEC
    • lid (fold) (acquired) — see also Disorder, eyelid, specified type NEC
    • ocular muscle (congenital) Q10.3
  • Excess, excessive, excessively
    • skin L98.7
      • eyelid (acquired) — see Blepharochalasis
  • Epiblepharon (congenital) Q10.3
  • Fold, folds (anomalous) — see also Anomaly, by site
  • Epicanthus, epicanthic fold (eyelid) (congenital) Q10.3
  • Malformation (congenital) — see also Anomaly
  • Hypoplasia, hypoplastic
    • eyelid (congenital) Q10.3
  • Insufficiency, insufficient
    • tarso-orbital fascia, congenital Q10.3
  • Narrowness, abnormal, eyelid Q10.3
Alongside this code 7 same parent — Q10
Additional references
AHA Coding Clinic® Licence required

Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.

Risk adjustment

Maps to no condition category in any loaded model.

Presence is a property of the code. Untick a model to hide it everywhere.

This code

Billable
yes
Code set
FY2026
Parent
Q10
Block
Q10-Q18
Siblings
7

Present FY2024–FY2027.