Other congenital malformation syndromes predominantly associated with short stature
Billable / specificPOA exempt
Q87.19 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Aarskog syndrome
- Cockayne syndrome
- De Lange syndrome
- Dubowitz syndrome
- Noonan syndrome
- Robinow-Silverman-Smith syndrome
- Russell-Silver syndrome
- Seckel syndrome
Includes (from Q87)
- Note: Codes from this chapter are not for use on maternal records
Excludes1
Not coded here — never report together with this code.
Excludes2
Not included here — may be reported together when both conditions exist.
Use additional code
Add a code to identify the following, if applicable.
- code(s) to identify all associated manifestations (from Q87)
Also known as
- Aarskog syndrome
- Cockayne syndrome
- De Lange syndrome
- Dubowitz syndrome
- Noonan syndrome
- Robinow-Silverman-Smith syndrome
- Russell-Silver syndrome
- Seckel syndrome
- Aarskog's syndrome
- Amsterdam dwarfism
- Bonnevie-Ullrich syndrome
- Bruck-de Lange disease
- Cockayne's syndrome
- Cornelia de Lange syndrome
- De Lange's syndrome
- Dubowitz' syndrome
- Noonan's syndrome
- Prader-Willi-like syndrome
- Seckel's syndrome
- Silver's syndrome
- Sjögren-Larsson syndrome
Parent code
- Q87.1Congenital malformation syndromes predominantly associated with short statureHeader
Related codes
- Q87.11Prader-Willi syndromeBillable