ICD-10-CM › Q00-QA1 › Q80-Q89 › Q87 Other specified congenital... › Q87.0
Congenital malformation syndromes predominantly affecting facial appearance
ValidICD-10-CM diagnosis code.
Valid for claims with a date of service in the current code year.
What has happened to this code
Every change the publisher made, from 2007 to now. Entries marked draft are from the pre-implementation releases: ICD-10 took effect on 1 October 2015, so nothing before FY2016 was ever valid on a claim.
- FY2007 Added to the draft code set draft Congenital malformation syndromes predominantly affecting facial appearance
Official coding rules
Published by CDC for FY2027. A rule attached to a category binds every code beneath it, so the rules inherited from this code's ancestors are shown with the code they come from.
Inherited from Q87 Other specified congenital malformation syndromes affecting multiple systems
Use additional code
- code(s) to identify all associated manifestations
How CDC's index refers to this code
Wording from the official alphabetic index. Much of it appears nowhere in the code description, which is why a search for the everyday phrase so often finds nothing.
- Cyclopism
- Robin syndrome
- Whistling face
- Mohr's syndrome
- Apert's syndrome
- Cyclopia, cyclops
- Fraser's syndrome
- Goldenhar syndrome
- Hanhart's syndrome
- Marchesani syndrome
- Carpenter's syndrome
- Acrocephalosyndactyly
- Syndrome > first arch
- Dyscranio-pygo-phalangy
- Freeman Sheldon syndrome
- Acrocephalopolysyndactyly
- Syndrome > whistling face
- Cryptophthalmos > syndrome
- Hallerman-Streiff syndrome
- Moebius, Möbius > syndrome
- Syndrome > cryptophthalmos
- Aglossia-adactylia syndrome
- Ullrich-Feichtiger syndrome
- Gorlin-Chaudry-Moss syndrome
- Dysplasia > oculodentodigital
- Syndrome > oro-facial-digital
- Syndrome > oral-facial-digital
- Syndrome > oto-palatal-digital
- Tower skull > with exophthalmos
- Syndrome > eyelid-malar-mandible
- Papillon-Léage and Psaume syndrome
- Pierre Robin deformity or syndrome
- Syndrome > micrognathia-glossoptosis
- Meyer-Schwickerath and Weyers syndrome
- Syndrome > congenital > facial diplegia
- Syndrome > congenital > oculofacial diplegia
- Paralysis, paralytic > oculofacial, congenital
- Syndrome > congenital > oculo-auriculovertebral
- Moebius, Möbius > syndrome > congenital oculofacial paralysis
Codes in the same group
| Code | Description | Status |
|---|---|---|
| Q87.1 | Congenital malformation syndromes predominantly associated with short stature | Not billable |
| Q87.2 | Congenital malformation syndromes predominantly involving limbs | Valid |
| Q87.3 | Congenital malformation syndromes involving early overgrowth | Valid |
| Q87.4 | Marfan syndrome | Not billable |
| Q87.5 | Other congenital malformation syndromes with other skeletal changes | Valid |
| Q87.8 | Other specified congenital malformation syndromes, not elsewhere classified | Not billable |
| Q87.A | Loeys-Dietz syndrome | Valid |