Other specified congenital malformation syndromes affecting multiple systems - Q87
Use Additional Code: This note indicates that an additional code should be used in conjunction with the primary code "Q87" to provide a complete picture of the patient's condition or to capture associated factors.
Use Additional:
- code(s) to identify all associated manifestations
These ranges represents subcategories of Other specified congenital malformation syndromes affecting multiple systems. The "Q87" signifies that these are the diseases within this broad category.
Codes:
- Q87.0 - Congenital malformation syndromes predominantly affecting facial appearance
- Q87.1 - Congenital malformation syndromes predominantly associated with short stature
- Q87.11 - Prader-Willi syndrome
- Q87.19 - Other congenital malformation syndromes predominantly associated with short stature
- Q87.2 - Congenital malformation syndromes predominantly involving limbs
- Q87.3 - Congenital malformation syndromes involving early overgrowth
- Q87.4 - Marfan syndrome
- Q87.40 - Marfan syndrome, unspecified
- Q87.41 - Marfan syndrome with cardiovascular manifestations
- Q87.410 - Marfan syndrome with aortic dilation
- Q87.418 - Marfan syndrome with other cardiovascular manifestations
- Q87.42 - Marfan syndrome with ocular manifestations
- Q87.43 - Marfan syndrome with skeletal manifestation
- Q87.5 - Other congenital malformation syndromes with other skeletal changes
- Q87.8 - Other specified congenital malformation syndromes, not elsewhere classified
- Q87.81 - Alport syndrome
- Q87.82 - Arterial tortuosity syndrome
- Q87.83 - Bardet-Biedl syndrome
- Q87.84 - Laurence-Moon syndrome
- Q87.85 - MED13L syndrome
- Q87.86 - Kleefstra syndrome
- Q87.89 - Other specified congenital malformation syndromes, not elsewhere classified