Q87.0
Congenital malformation syndromes predominantly affecting facial appearance
Billable FY2026 2025-10-01 → 2026-09-30
Instructional notes 10
Index entries leading here 28
- Acrocephalopolysyndactyly Q87.0
- Acrocephalosyndactyly Q87.0
- Aglossia-adactylia syndrome Q87.0
- Apert's syndrome Q87.0
- Carpenter's syndrome Q87.0
- Syndrome — see also Disease
- Moebius, Möbius
- Cryptophthalmos Q11.2
- syndrome Q87.0
- Cyclopia, cyclops Q87.0
- Cyclopism Q87.0
- Dyscranio-pygo-phalangy Q87.0
- Dysplasia — see also Anomaly
- oculodentodigital Q87.0
- Fraser's syndrome Q87.0
- Freeman Sheldon syndrome Q87.0
- Goldenhar (-Gorlin) syndrome Q87.0
- Gorlin-Chaudry-Moss syndrome Q87.0
- Hallerman-Streiff syndrome Q87.0
- Hanhart's syndrome Q87.0
- Marchesani (-Weill) syndrome Q87.0
- Meyer-Schwickerath and Weyers syndrome Q87.0
- Mohr's syndrome (Types I and II) Q87.0
- Paralysis, paralytic (complete) (incomplete) G83.9
- oculofacial, congenital (Moebius) Q87.0
- Papillon-Léage and Psaume syndrome Q87.0
- Pierre Robin deformity or syndrome Q87.0
- Robin (-Pierre) syndrome Q87.0
- Tower skull Q75.058
- with exophthalmos Q87.0
- Ullrich-Feichtiger syndrome Q87.0
- Whistling face Q87.0
Alongside this code 6 same parent — Q87
Q87.1 Congenital malform syndromes predom assoc w short stature category Q87.2 Congenital malformation syndromes predom involving limbs Q87.3 Congenital malformation syndromes involving early overgrowth Q87.4 Marfan syndrome category Q87.5 Oth congenital malformation syndromes w oth skeletal changes Q87.8 Oth congenital malformation syndromes, NEC category
Additional references
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