 Q87 |
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Other specified congenital malformation syndromes affecting multiple systems  |
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| UseAdditionalCode |
code(s) to identify all associated manifestations
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 Q87.0 |
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Congenital malformation syndromes predominantly affecting facial appearance |
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| Acrocephalopolysyndactyly | | Acrocephalosyndactyly [Apert] | | Cryptophthalmos syndrome | | Cyclopia | | Goldenhar syndrome | | Moebius syndrome | | Oro-facial-digital syndrome | | Robin syndrome | | Whistling face |
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| Q87.1 |
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Congenital malformation syndromes predominantly associated with short stature |
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| Excludes1 |
Ellis-van Creveld syndrome (Q77.6)
Smith-Lemli-Opitz syndrome (E78.72)
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| Q87.11 |
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Prader-Willi syndrome |
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| Q87.19 |
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Other congenital malformation syndromes predominantly associated with short stature |
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| Aarskog syndrome | | Cockayne syndrome | | De Lange syndrome | | Dubowitz syndrome | | Noonan syndrome | | Robinow-Silverman-Smith syndrome | | Russell-Silver syndrome | | Seckel syndrome |
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| Q87.2 |
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Congenital malformation syndromes predominantly involving limbs |
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| Holt-Oram syndrome | | Klippel-Trenaunay-Weber syndrome | | Nail patella syndrome | | Rubinstein-Taybi syndrome | | Sirenomelia syndrome | | Thrombocytopenia with absent radius [TAR] syndrome | | VATER syndrome |
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| Q87.3 |
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Congenital malformation syndromes involving early overgrowth |
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| Beckwith-Wiedemann syndrome | | Sotos syndrome | | Weaver syndrome |
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| Q87.4 |
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Marfan syndrome |
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| Q87.40 |
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Marfan syndrome, unspecified |
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| Q87.41 |
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Marfan syndrome with cardiovascular manifestations |
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| Q87.410 |
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Marfan syndrome with aortic dilation |
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| Q87.418 |
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Marfan syndrome with other cardiovascular manifestations |
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| Q87.42 |
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Marfan syndrome with ocular manifestations |
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| Q87.43 |
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Marfan syndrome with skeletal manifestation |
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| Q87.5 |
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Other congenital malformation syndromes with other skeletal changes |
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| Q87.8 |
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Other specified congenital malformation syndromes, not elsewhere classified |
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| Excludes1 |
Zellweger syndrome (E71.510)
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| Q87.81 |
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Alport syndrome |
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| UseAdditionalCode |
code to identify stage of chronic kidney disease (N18.1-N18.6)
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| Q87.82 |
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Arterial tortuosity syndrome |
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| Q87.83 |
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Bardet-Biedl syndrome |
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| Q87.84 |
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Laurence-Moon syndrome |
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| Q87.85 |
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MED13L syndrome |
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| Asadollahi-Rauch syndrome | | Mediator complex subunit 13L syndrome |
| CodeAlso |
, if applicable, any associated manifestations such as:
autism spectrum disorder (F84.0-)
congenital malformations of cardiac septa (Q21.-)
epilepsy and recurrent seizures (G40.-)
intellectual disability (F70-F79)
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| Q87.86 |
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Kleefstra syndrome |
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| Q87.87 |
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Hao-Fountain Syndrome |
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| HAFOUS |
| UseAdditionalCode |
code, if applicable, for associated conditions such as:
autism spectrum disorder (F84.0)
developmental speech disorder (F80.-)
epilepsy, by specific type (G40.-)
intellectual disabilities (F70-F79)
pervasive developmental disorders (F84.-)
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| Q87.88 |
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CTNNB1 syndrome |
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| UseAdditionalCode |
code, if applicable, for associated conditions such as:
cerebral palsy (G80.-)
congenital heart malformations (Q20.0-Q24.9)
developmental disorder of speech and language (F80.-)
exudative retinopathy (H35.02-)
intellectual disability (F70-F79)
microcephaly (Q02)
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| Q87.89 |
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Other specified congenital malformation syndromes, not elsewhere classified |
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