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

syndromes icd 10
 
malformation icd 10
 
congenital icd 10
 
stature icd 10
 
short icd 10
 
predominantly icd 10
 
associated icd 10
 
Non-Billable/Non-Specific Code

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