Q87.1

The ICD-10-CM code for congenital malform syndromes predom assoc w short stature is Q87.1. The full clinical description is "Congenital malformation syndromes predominantly associated with short stature". Q87.1 is a non-billable header code. Use a more specific child code for billing purposes.

ICD-10-CM code Q87.1 represents “Congenital malformation syndromes predominantly associated with short stature”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a non-billable header code. Use a more specific child code for billing purposes.

No, Q87.1 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 2 child codes under Q87.1.

Q87.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

Q87.1 has Excludes1 notes indicating codes that cannot be used together with it, including: Ellis-van Creveld syndrome (Q77.6); Smith-Lemli-Opitz syndrome (E78.72).

Q87.1 has 2 child codes, including: Q87.11 (Prader-Willi syndrome), Q87.19 (Other congen malform synd predom assoc with short stature).

Yes, when using Q87.1, also report: code(s) to identify all associated manifestations.

Q87.1 is linked to 1 UMLS Concept Unique Identifier: C0347915. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malform syndromes predom assoc w short stature affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

Q87.1 maps to the ICD-11 code: LD2Z (Multiple developmental anomalies or syndromes, unspecified).