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Q87.2

Congenital malformation syndromes predominantly involving limbs

Billable FY2026 2025-10-01 → 2026-09-30
Instructional notes 8
Q87code
Use additional code
  • code(s) to identify all associated manifestations
Q87.2code
Inclusion terms
  • Holt-Oram syndrome
  • Klippel-Trenaunay-Weber syndrome
  • Nail patella syndrome
  • Rubinstein-Taybi syndrome
  • Sirenomelia syndrome
  • Thrombocytopenia with absent radius [TAR] syndrome
  • VATER syndrome
Index entries leading here 17
  • Syndrome — see also Disease
    • Fong's Q87.2
    • nail patella Q87.2
    • Osterreicher-Turner Q87.2
    • sirenomelia Q87.2
    • TAR (thrombocytopenia with absent radius) Q87.2
    • thrombocytopenia with absent radius (TAR) Q87.2
    • VATER Q87.2
  • Fong's syndrome (hereditary osteo-onychodysplasia) Q87.2
  • Holt-Oram syndrome Q87.2
  • Klippel-Trenaunay (-Weber) syndrome Q87.2
  • Mietens' syndrome Q87.2
  • Nail — see also condition
  • Onycho-osteodysplasia Q87.2
  • Osteo-onycho-arthro-dysplasia Q87.2
  • Osteo-onychodysplasia, hereditary Q87.2
  • Österreicher-Turner syndrome Q87.2
  • Rubinstein-Taybi syndrome Q87.2
  • Sirenomelia (syndrome) Q87.2
  • TAR (thrombocytopenia with absent radius) syndrome Q87.2
  • Taybi's syndrome Q87.2
  • Thrombocytopenia, thrombocytopenic D69.6
    • with absent radius (TAR) Q87.2
  • Turner-Kieser syndrome Q87.2
  • VATER syndrome Q87.2
Alongside this code 6 same parent — Q87
Additional references
AHA Coding Clinic® Licence required

Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.

Risk adjustment

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This code

Billable
yes
Code set
FY2026
Parent
Q87
Block
Q80-Q89
Siblings
6

Present FY2024–FY2027.