| ICD-10-CM-2023 > Q00-Q99 > Q80-Q89 > Q87 |
Q80-Q89 | Other congenital malformations | |
Q87 | Other specified congenital malformation syndromes affecting multiple systems | |
Use add'l | code(s) to identify all associated manifestations | |
Q87.0 | Congenital malformation syndromes predominantly affecting facial appearance | |
Info: | Acrocephalopolysyndactyly Acrocephalosyndactyly [Apert] Cryptophthalmos syndrome Cyclopia Goldenhar syndrome Moebius syndrome Oro-facial-digital syndrome Robin syndrome Whistling face | |
Q87.1 | Congenital malformation syndromes predominantly associated with short stature | |
Excl1.: | Ellis-van Creveld syndrome (Q77.6) Smith-Lemli-Opitz syndrome (E78.72) | |
Q87.11 | Prader-Willi syndrome | |
Q87.19 | Other congenital malformation syndromes predominantly associated with short stature | |
Info: | Aarskog syndrome Cockayne syndrome De Lange syndrome Dubowitz syndrome Noonan syndrome Robinow-Silverman-Smith syndrome Russell-Silver syndrome Seckel syndrome | |
Q87.2 | Congenital malformation syndromes predominantly involving limbs | |
Info: | Holt-Oram syndrome Klippel-Trenaunay-Weber syndrome Nail patella syndrome Rubinstein-Taybi syndrome Sirenomelia syndrome Thrombocytopenia with absent radius [TAR] syndrome VATER syndrome | |
Q87.3 | Congenital malformation syndromes involving early overgrowth | |
Info: | Beckwith-Wiedemann syndrome Sotos syndrome Weaver syndrome | |
Q87.4 | Marfan's syndrome | |
Q87.40 | Marfan's syndrome, unspecified | |
Q87.41 | Marfan's syndrome with cardiovascular manifestations | |
Q87.410 | Marfan's syndrome with aortic dilation | |
Q87.418 | Marfan's syndrome with other cardiovascular manifestations | |
Q87.42 | Marfan's syndrome with ocular manifestations | |
Q87.43 | Marfan's syndrome with skeletal manifestation | |
Q87.5 | Other congenital malformation syndromes with other skeletal changes | |
Q87.8 | Other specified congenital malformation syndromes, not elsewhere classified | |
Excl1.: | Zellweger syndrome (E71.510) | |
Q87.81 | Alport syndrome | |
Use add'l | code to identify stage of chronic kidney disease (N18.1-N18.6) | |
Q87.82 | Arterial tortuosity syndrome | |
Q87.89 | Other specified congenital malformation syndromes, not elsewhere classified | |
Info: | Laurence-Moon (-Bardet)-Biedl syndrome | |
|
ICD-10-CM-2023 Code Search Engine and PCS-2023 Code Search Engine |