Q78.3
BillableProgressive diaphyseal dysplasia
Progressive diaphyseal dysplasia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Camurati-Engelmann syndrome
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(8)
Q78.0Osteogenesis imperfecta
Q78.1Polyostotic fibrous dysplasia
Q78.2Osteopetrosis
Q78.4Enchondromatosis
Q78.5Metaphyseal dysplasia
Q78.6Multiple congenital exostoses
Q78.8Other specified osteochondrodysplasias
Q78.9Osteochondrodysplasia, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(100)
SNOMED CT
- Camurati-Engelmann syndrome34643004
- Diaphyseal dysplasia34643004
- Diaphyseal sclerosis34643004
- Engelman's disease34643004
- Engelmann syndrome34643004
- Engelmann's disease34643004
- Osteopathia hyperostotica multiplex infantis34643004
- Progressive diaphyseal dysplasia34643004
- CDD - Craniodiaphyseal dysplasia205506004
- Craniodiaphyseal dysplasia205506004
- Diaphyseal dysplasia anaemia syndrome389214003
- Diaphyseal dysplasia anemia syndrome389214003
- Diaphyseal dysplasia with anaemia389214003
- Diaphyseal dysplasia with anemia389214003
- Ghosal haematodiaphyseal dysplasia389214003
- Ghosal hematodiaphyseal dysplasia389214003
- Ghosal syndrome389214003
- Diaphyseal medullary stenosis with bone malignancy389216001
UMLS
- CAENDC0011989
- CAMURATI-ENGELMANN DISEASEC0011989
- CEDC0011989
- Camurati Engelmann DiseaseC0011989
- Camurati Engelmann SyndromeC0011989
- Camurati-Engelmann DiseaseC0011989
- Camurati-Engelmann SyndromeC0011989
- Camurati-Engelmann diseaseC0011989
- Camurati-Engelmann syndromeC0011989
- DIAPHYSEAL DYSPLASIA 1, PROGRESSIVEC0011989
- DPD1C0011989
- Diaphyseal Dysplasia 1, ProgressiveC0011989
- Diaphyseal Dysplasia, ProgressiveC0011989
- Diaphyseal Dysplasias, ProgressiveC0011989
- Diaphyseal HyperostosesC0011989
- Diaphyseal HyperostosisC0011989
- Diaphyseal dysplasiaC0011989
- Diaphyseal dysplasia (disorder)C0011989
- Diaphyseal hyperostosisC0011989
- Diaphyseal sclerosisC0011989
- Dysplasia, Progressive DiaphysealC0011989
- Dysplasias, Progressive DiaphysealC0011989
- ENGELMANN DISC0011989
- ENGELMANN DISEASEC0011989
- ENGELMANNS DISC0011989
- Engelman's diseaseC0011989
- Engelmann DiseaseC0011989
- Engelmann diseaseC0011989
- Engelmann syndromeC0011989
- Engelmann's DiseaseC0011989
- Engelmann's diseaseC0011989
- Hyperostoses, DiaphysealC0011989
- Hyperostosis, DiaphysealC0011989
- Osteopathia hyperostotica multiplex infantisC0011989
- PDDC0011989
- PROGRESSIVE DIAPHYSEAL DYSPLASIAC0011989
- Progressive Diaphyseal DysplasiaC0011989
- Progressive diaphyseal dysplasiaC0011989
- camurati engelmanns diseaseC0011989
- camurati-engelmann diseaseC0011989
- diaphyseal dysplasiaC0011989
- engelmann diseaseC0011989
- engelmann syndromeC0011989
- engelmann's diseaseC0011989
Clinical Terms
- ENGELMANN DIS
- CED
- Diaphyseal dysplasia
- DIAPHYSEAL DYSPLASIA 1, PROGRESSIVE
- Engelman's disease
- Engelmann syndrome
- Ghosal haematodiaphyseal dysplasia
- Diaphyseal dysplasia with anemia
- Diaphyseal dysplasia with anaemia
- Diaphyseal medullary stenosis with bone malignancy
- Diaphyseal Dysplasia, Progressive
- Engelmann Disease
- camurati engelmanns disease
- ENGELMANNS DIS
- Ghosal syndrome
- CAEND
- Diaphyseal Hyperostoses
- Engelmann's Disease
- Camurati-Engelmann syndrome
- Ghosal hematodiaphyseal dysplasia
- Osteopathia hyperostotica multiplex infantis
- Diaphyseal sclerosis
- Camurati-Engelmann Disease
- Diaphyseal Dysplasias, Progressive
- Hyperostosis, Diaphyseal
- Diaphyseal dysplasia anemia syndrome
- Diaphyseal dysplasia anaemia syndrome
- Camurati Engelmann Disease
- Camurati Engelmann Syndrome
- Diaphyseal hyperostosis
- Dysplasia, Progressive Diaphyseal
- Diaphyseal dysplasia (disorder)
- Dysplasias, Progressive Diaphyseal
- Craniodiaphyseal dysplasia
- CDD - Craniodiaphyseal dysplasia
- Hyperostoses, Diaphyseal
- PDD
- DPD1
Frequently Asked Questions
What is the ICD-10 code for progressive diaphyseal dysplasia?
The ICD-10-CM code for progressive diaphyseal dysplasia is Q78.3. The full clinical description is "Progressive diaphyseal dysplasia". Q78.3 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q78.3 mean?
ICD-10-CM code Q78.3 represents “Progressive diaphyseal dysplasia”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.
Is Q78.3 a billable code?
Yes, Q78.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q78.3 in?
Q78.3 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q78.3 map to?
Q78.3 maps to 4 SNOMED CT concepts: 205506004, 34643004, 389214003, 389216001. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q78.3?
Q78.3 is linked to 1 UMLS Concept Unique Identifier: C0011989. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q78.3 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like progressive diaphyseal dysplasia affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of Q78.3?
Q78.3 maps to the ICD-11 code: LD24.1Y (Other specified bone diseases with increased bone density).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.