Q87.1 Congenital malformation syndromes predominantly associated with short stature

Non-billable header with 2 child codes.

Excludes1 (never code together)

• Ellis-van Creveld syndrome (Q77.6)
• Smith-Lemli-Opitz syndrome (E78.72)

Applies from Q87 Other specified congenital malformation syndromes affecting multiple systems

Use additional code

• code(s) to identify all associated manifestations

Codes under Q87.1

• Q87.11 Prader-Willi syndrome
• Q87.19 Other congenital malformation syndromes predominantly associated with short stature

Approximate ICD-9-CM (GEMs)

• 759.81 Prader-Willi syndrome (approximate)

Code annotations containing back-references to Q87.1

Back-references to Q87

• Type 1 Excludes: Q67 Congenital musculoskeletal deformities of head, face, spine and chest ("congenital malformation syndromes classified to Q87.-")
• Type 1 Excludes: Q75 Other congenital malformations of skull and face bones ("congenital malformation syndromes classified to Q87.-")
• Type 1 Excludes: Q89.7 Multiple congenital malformations, not elsewhere classified ("congenital malformation syndromes affecting multiple systems (Q87.-)")

Nearby codes

• Q87 Other specified congenital malformation syndromes affecting multiple systems
• Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
• Q87.1 Congenital malformation syndromes predominantly associated with short stature (this code)
• 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