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ICD-10-CM Codes
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Q00-Q99
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Q65-Q79
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Q78-
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2023 ICD-10-CM Diagnosis Code Q78.3
2023 ICD-10-CM Diagnosis Code Q78.3
Progressive diaphyseal dysplasia
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt
- Q78.3 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM Q78.3 became effective on October 1, 2022.
- This is the American ICD-10-CM version of Q78.3 - other international versions of ICD-10 Q78.3 may differ.
Applicable To- Camurati-Engelmann syndrome
The following code(s) above
Q78.3 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
Q78.3:
- Multiple epiphyseal dysplasia
Clinical Information
- An autosomal dominant form of dysplasia that is characterized by progressive thickening of diaphyseal cortex of long bones. Mutations in the gene that encodes transforming growth factor beta1 are one cause of this disorder.
- An autosomal dominant skeletal disorder caused by mutations in the tgfb1 gene. It is characterized by thickening of the bones, particularly the long bones of the extremities. It is associated with muscle weakness and tiredness.
Present On AdmissionPOA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
- Q78.3 is considered exempt from POA reporting.
ICD-10-CM Q78.3 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 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
Convert Q78.3 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- Camurati-Engelmann syndrome Q78.3
- Dysplasia - see also Anomaly
- fibrous
- diaphyseal, progressive Q78.3
- diaphyseal, progressive Q78.3
- Engelmann Q78.3 (-Camurati)
ICD-10-CM Codes Adjacent To Q78.3
Q77.5 Diastrophic dysplasia
Q77.6 Chondroectodermal dysplasia
Q77.7 Spondyloepiphyseal dysplasia
Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine
Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified
Q78 Other osteochondrodysplasias
Q78.0 Osteogenesis imperfecta
Q78.1 Polyostotic fibrous dysplasia
Q78.3
Progressive diaphyseal dysplasia
Q78.5 Metaphyseal dysplasia
Q78.6 Multiple congenital exostoses
Q78.8 Other specified osteochondrodysplasias
Q78.9 Osteochondrodysplasia, unspecified
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified
Q79.0 Congenital diaphragmatic hernia
Q79.1 Other congenital malformations of diaphragm
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
