Q87.19CurrentBillable / specificExempt from present-on-admission reporting

Other congenital malformation syndromes predominantly associated with short stature

Q87 · Inherited instructions

Use additional code

code(s) to identify all associated manifestations

Q87.1 · Inherited instructions

Excludes 1

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

Excludes 2 · 1

Chapters 17 · Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0)

Excludes 2

inborn errors of metabolism (E70-E88)

Claims & coverage

Coverage depends on the payer, service and applicable policy. A billable code does not guarantee payment.

When ICD-10-CM is required

For US diagnosis claims covered by HIPAA, ICD-10-CM is required from October 1, 2015.

Use the service date for outpatient/professional claims and the discharge date for hospital inpatient claims. Earlier encounters use ICD-9-CM; each individual code must also be valid for the applicable date.

Official coding guidelines → · CMS ↗

MS-DRG · 43.1 · 564, 565, 566

Grouping depends on the complete encounter and CMS grouper logic.

564 · Other Musculoskeletal System and Connective Tissue Diagnoses with MCC
565 · Other Musculoskeletal System and Connective Tissue Diagnoses with CC
566 · Other Musculoskeletal System and Connective Tissue Diagnoses without CC/MCC

2026-04-01 – 2026-09-30

CMS · MS-DRG 43.1

Check Medicare coverage ↗

First observed · 2019-10-01

Code history

Latest recorded change · FY2020

ChangedUnchanged

FY2020

Effective from 2019-10-01

Added

Other congenital malformation syndromes predominantly associated with short stature

Billable diagnosis code

CDC/NCHS · FY2020

All editions (15)

All editions	Effective from	Code history
FY2020	2019-10-01	Added
FY2020 · April	2020-04-01	No tabular change
FY2021	2020-10-01	No tabular change
FY2021 · 01-01	2021-01-01	No tabular change
FY2022	2021-10-01	No tabular change
FY2022 · 04-01	2022-04-01	No tabular change
FY2023	2022-10-01	No tabular change
FY2023 · 04-01	2023-04-01	No tabular change
FY2024	2023-10-01	No tabular change
FY2024 · 04-01	2024-04-01	No tabular change
FY2025	2024-10-01	No tabular change
FY2025 · 04-01	2025-04-01	No tabular change
FY2026	2025-10-01	No tabular change
FY2026 · April	2026-04-01	No tabular change
FY2027	2026-10-01	No tabular change

Code-level instructions

Includes

Aarskog syndrome
Cockayne syndrome
De Lange syndrome
Dubowitz syndrome
Noonan syndrome
Robinow-Silverman-Smith syndrome
Russell-Silver syndrome
Seckel syndrome

Inherited instructions

Q87 · Other specified congenital malformation syndromes affecting multiple systems

Use additional code

code(s) to identify all associated manifestations

Chapters 17 · Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0)

Excludes 2

inborn errors of metabolism (E70-E88)

Note

Codes from this chapter are not for use on maternal records

Q87.1 · Congenital malformation syndromes predominantly associated with short stature

Excludes 1

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

Official index references (20)

Aarskog's syndrome (1)

Aarskog's syndromeDisease index

Amsterdam dwarfism (1)

Amsterdam dwarfismDisease index

Bonnevie-Ullrich syndrome (1)

Bonnevie-Ullrich syndromeDisease index

Bruck-de Lange disease (1)

Bruck-de Lange diseaseDisease index

Cockayne's syndrome (1)

Cockayne's syndromeDisease index

Cornelia de Lange syndrome (1)

Cornelia de Lange syndromeDisease index

De Lange's syndrome (1)

De Lange's syndromeDisease index

Dubowitz' syndrome (1)

Dubowitz' syndromeDisease index

Noonan's syndrome (1)

Noonan's syndromeDisease index

Prader-Willi-like syndrome (1)

Prader-Willi-like syndromeDisease index

Robinow-Silverman-Smith syndrome (1)

Robinow-Silverman-Smith syndromeDisease index

Russell-Silver syndrome (1)

Russell-Silver syndromeDisease index

Seckel's syndrome (1)

Seckel's syndromeDisease index

Silver's syndrome (1)

Silver's syndromeDisease index

Sjögren-Larsson syndrome (1)

Sjögren-Larsson syndromeDisease index

Syndrome (2)

Syndrome › Prader-Willi-likeDisease index
Syndrome › pseudo -Turner'sDisease index

Turner-like syndrome (1)

Turner-like syndromeDisease index

Ullrich(-Bonnevie)(-Turner) syndrome (1)

Ullrich(-Bonnevie)(-Turner) syndromeDisease index

Weil(l)-Marchesani syndrome (1)

Weil(l)-Marchesani syndromeDisease index

Official conversion history

Historical assignments from the CDC conversion table support data retrieval. They do not authorize substituting a previous code for the current code.

Release dates 2019-10-01

Previous assignment: Q87.1

Related codes

Other entries in the same category; these are not automatic substitutes.

Code	Description	Category · further specificity required
Q87.11	Prader-Willi syndrome	Billable / specific

Official titles and instructions are preserved in their source language. Official sources ↗

Q87.19CurrentBillable / specificExempt from present-on-admission reporting

Other congenital malformation syndromes predominantly associated with short stature

Q87 · Inherited instructions

Use additional code

code(s) to identify all associated manifestations

Q87.1 · Inherited instructions

Excludes 1

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

Excludes 2 · 1

Chapters 17 · Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0)

Excludes 2

inborn errors of metabolism (E70-E88)

Claims & coverage

Coverage depends on the payer, service and applicable policy. A billable code does not guarantee payment.

When ICD-10-CM is required

For US diagnosis claims covered by HIPAA, ICD-10-CM is required from October 1, 2015.

Official coding guidelines → · CMS ↗

MS-DRG · 43.1 · 564, 565, 566

Grouping depends on the complete encounter and CMS grouper logic.

564 · Other Musculoskeletal System and Connective Tissue Diagnoses with MCC
565 · Other Musculoskeletal System and Connective Tissue Diagnoses with CC
566 · Other Musculoskeletal System and Connective Tissue Diagnoses without CC/MCC

2026-04-01 – 2026-09-30

CMS · MS-DRG 43.1

Check Medicare coverage ↗

First observed · 2019-10-01

Code history

Latest recorded change · FY2020

ChangedUnchanged

FY2020

Effective from 2019-10-01

Added

Other congenital malformation syndromes predominantly associated with short stature

Billable diagnosis code

CDC/NCHS · FY2020

All editions (15)

All editions	Effective from	Code history
FY2020	2019-10-01	Added
FY2020 · April	2020-04-01	No tabular change
FY2021	2020-10-01	No tabular change
FY2021 · 01-01	2021-01-01	No tabular change
FY2022	2021-10-01	No tabular change
FY2022 · 04-01	2022-04-01	No tabular change
FY2023	2022-10-01	No tabular change
FY2023 · 04-01	2023-04-01	No tabular change
FY2024	2023-10-01	No tabular change
FY2024 · 04-01	2024-04-01	No tabular change
FY2025	2024-10-01	No tabular change
FY2025 · 04-01	2025-04-01	No tabular change
FY2026	2025-10-01	No tabular change
FY2026 · April	2026-04-01	No tabular change
FY2027	2026-10-01	No tabular change

Code-level instructions

Includes

Aarskog syndrome
Cockayne syndrome
De Lange syndrome
Dubowitz syndrome
Noonan syndrome
Robinow-Silverman-Smith syndrome
Russell-Silver syndrome
Seckel syndrome

Inherited instructions

Q87 · Other specified congenital malformation syndromes affecting multiple systems

Use additional code

code(s) to identify all associated manifestations

Chapters 17 · Congenital malformations, deformations and chromosomal abnormalities (Q00-QA0)

Excludes 2

inborn errors of metabolism (E70-E88)

Note

Codes from this chapter are not for use on maternal records

Q87.1 · Congenital malformation syndromes predominantly associated with short stature

Excludes 1

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

Official index references (20)

Aarskog's syndrome (1)

Aarskog's syndromeDisease index

Amsterdam dwarfism (1)

Amsterdam dwarfismDisease index

Bonnevie-Ullrich syndrome (1)

Bonnevie-Ullrich syndromeDisease index

Bruck-de Lange disease (1)

Bruck-de Lange diseaseDisease index

Cockayne's syndrome (1)

Cockayne's syndromeDisease index

Cornelia de Lange syndrome (1)

Cornelia de Lange syndromeDisease index

De Lange's syndrome (1)

De Lange's syndromeDisease index

Dubowitz' syndrome (1)

Dubowitz' syndromeDisease index

Noonan's syndrome (1)

Noonan's syndromeDisease index

Prader-Willi-like syndrome (1)

Prader-Willi-like syndromeDisease index

Robinow-Silverman-Smith syndrome (1)

Robinow-Silverman-Smith syndromeDisease index

Russell-Silver syndrome (1)

Russell-Silver syndromeDisease index

Seckel's syndrome (1)

Seckel's syndromeDisease index

Silver's syndrome (1)

Silver's syndromeDisease index

Sjögren-Larsson syndrome (1)

Sjögren-Larsson syndromeDisease index

Syndrome (2)

Syndrome › Prader-Willi-likeDisease index
Syndrome › pseudo -Turner'sDisease index

Turner-like syndrome (1)

Turner-like syndromeDisease index

Ullrich(-Bonnevie)(-Turner) syndrome (1)

Ullrich(-Bonnevie)(-Turner) syndromeDisease index

Weil(l)-Marchesani syndrome (1)

Weil(l)-Marchesani syndromeDisease index

Official conversion history

Historical assignments from the CDC conversion table support data retrieval. They do not authorize substituting a previous code for the current code.

Release dates 2019-10-01

Previous assignment: Q87.1

Related codes

Other entries in the same category; these are not automatic substitutes.

Code	Description	Category · further specificity required
Q87.11	Prader-Willi syndrome	Billable / specific

Official titles and instructions are preserved in their source language. Official sources ↗