Q78.1
BillablePolyostotic fibrous dysplasia
Polyostotic fibrous dysplasia
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Albright(-McCune)(-Sternberg) syndrome
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(8)
Q78.0Osteogenesis imperfecta
Q78.2Osteopetrosis
Q78.3Progressive diaphyseal dysplasia
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(102)
SNOMED CT
- Albright syndrome36517007
- Albright's disease of bone36517007
- Osteitis fibrosa disseminata36517007
- PFD - Polyostotic fibrous dysplasia36517007
- POFD - Polyostotic fibrous dysplasia36517007
- Polyostotic fibrous dysplasia36517007
- Polyostotic fibrous dysplasia of bone36517007
- Cafe au lait spots201281002
- Cafe-au-lait spots201281002
- Café au lait spot201281002
- Café au lait spots201281002
- McCune Albright syndrome726029005
UMLS
- ALBRIGHT SYNDROMEC0242292
- Albright SyndromeC0242292
- Albright syndromeC0242292
- Albright's DiseaseC0242292
- Albright's Disease of BoneC0242292
- Albright's SyndromeC0242292
- Albright's Syndrome with Precocious PubertyC0242292
- Albright's diseaseC0242292
- Albright's disease of boneC0242292
- Albright's syndromeC0242292
- Albright's syndrome with precocious pubertyC0242292
- Albright(-McCune)(-Sternberg) syndromeC0242292
- Albright-McCune-Sternberg syndromeC0242292
- Albright-Mccune-Sternberg SyndromeC0242292
- Albright-Sternberg SyndromeC0242292
- Albright-Sternberg syndromeC0242292
- Fibrous Dysplasia with Pigmentary Skin Changes and Precocious PubertyC0242292
- Fibrous dysplasia with pigmentary skin changes and precocious pubertyC0242292
- MASC0242292
- MCCUNE-ALBRIGHT SYNDROMEC0242292
- McCune Albright SyndromeC0242292
- McCune Albright syndromeC0242292
- McCune Albright syndrome (disorder)C0242292
- McCune-Albright SyndromeC0242292
- McCune-Albright syndromeC0242292
- Syndrome, AlbrightC0242292
- Syndrome, Albright'sC0242292
- Syndrome, McCune-AlbrightC0242292
- albright diseaseC0242292
- albright syndromeC0242292
- albright's diseaseC0242292
- albright's disease boneC0242292
- albright's syndromeC0242292
- albrights mccune syndromeC0242292
- albrights syndromeC0242292
- mccune albright syndromeC0242292
- mccune-albright syndromeC0242292
- Dysplasia, Polyostotic FibrousC0016065
- Dysplasias, Polyostotic FibrousC0016065
- Fibrous Dysplasia, PolyostoticC0016065
- Fibrous Dysplasias, PolyostoticC0016065
- Osteitis fibrosa disseminataC0016065
- PFDC0016065
- PFD - Polyostotic fibrous dysplasiaC0016065
- POFDC0016065
- POFD - Polyostotic fibrous dysplasiaC0016065
- POLYOSTOTIC FIBROUS DYSPLASIAC0016065
- Polyostotic Fibrous DysplasiaC0016065
- Polyostotic Fibrous Dysplasia of BoneC0016065
- Polyostotic Fibrous DysplasiasC0016065
- Polyostotic fibrous dysplasiaC0016065
- Polyostotic fibrous dysplasia of boneC0016065
- Polyostotic fibrous dysplasia of bone (disorder)C0016065
- polyostotic fibrous dysplasiaC0016065
Clinical Terms
- Dysplasia, Polyostotic Fibrous
- Cafe au lait spots
- albright's disease bone
- PFD
- Albright's disease of bone
- Café au lait spot
- ALBRIGHT SYNDROME
- McCune Albright Syndrome
- PFD - Polyostotic fibrous dysplasia
- Dysplasias, Polyostotic Fibrous
- McCune-Albright Syndrome
- albright's disease
- albrights syndrome
- Albright's syndrome
- Albright-Sternberg syndrome
- MAS
- Albright(-McCune)(-Sternberg) syndrome
- Fibrous Dysplasia with Pigmentary Skin Changes and Precocious Puberty
- Osteitis fibrosa disseminata
- Polyostotic fibrous dysplasia of bone (disorder)
- Syndrome, Albright's
- POFD
- Polyostotic Fibrous Dysplasia of Bone
- Fibrous Dysplasia, Polyostotic
- Fibrous Dysplasias, Polyostotic
- Syndrome, McCune-Albright
- Albright-McCune-Sternberg syndrome
- Café au lait spots
- albrights mccune syndrome
- McCune Albright syndrome (disorder)
- Syndrome, Albright
- POFD - Polyostotic fibrous dysplasia
- Albright's syndrome with precocious puberty
- albright disease
- Cafe-au-lait spots
- Polyostotic Fibrous Dysplasias
Frequently Asked Questions
What is the ICD-10 code for polyostotic fibrous dysplasia?
The ICD-10-CM code for polyostotic fibrous dysplasia is Q78.1. The full clinical description is "Polyostotic fibrous dysplasia". Q78.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q78.1 mean?
ICD-10-CM code Q78.1 represents “Polyostotic fibrous 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 Q78.1 a billable code?
Yes, Q78.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q78.1 in?
Q78.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What SNOMED CT codes does Q78.1 map to?
Q78.1 maps to 3 SNOMED CT concepts: 36517007, 201281002, 726029005. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q78.1?
Q78.1 is linked to 2 UMLS Concept Unique Identifiers: C0242292, C0016065. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q78.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like polyostotic fibrous 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 Q78.1?
Q78.1 maps to the ICD-11 code: FB80.0 (Fibrous dysplasia of bone).
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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.