Q87.1 - Congenital malformation syndromes predominantly associated with short stature
- Applicable to Congenital malformation syndromes predominantly associated with short stature
- The 2025 edition of ICD10-CM Q87.1 became effective on October 1, 2024.
- This is the American ICD10-CM version of Q87.1 - other international versions of ICD10 Q87.1 may differ.
- Q87.1 is a Non-Billable / Non-Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- Q87.1 Code should not be used for billing or reimbursement purposes as there are multiple ICD-10 CM codes below it that contain a greater level of detail.
- Q87.1 - Congenital malformation syndromes predominantly associated with short stature
- 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
Type 1 Excludes
- Ellis-van Creveld syndrome (Q77.6)
- Smith-Lemli-Opitz syndrome (E78.72)
The following codes above Q87.1 contain annotation back-references that may be applicable to Q87.1:
Chapter: Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities
Section: Q80-Q89 Other congenital malformations
Category: Q87 Other specified congenital malformation syndromes affecting multiple systems
Non-Billable/Non-Specific Code
Browse other similar CM codes
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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