Q78.3
BillableProgressive diaphyseal dysplasia
Progressive diaphyseal dysplasia
Status
Billable / Specific
Parent Code
Q78Coding Notes
Also Known As / Clinical Terms
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
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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.