Q75.1
BillableCraniofacial dysostosis
Craniofacial dysostosis
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Crouzon's disease
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •congenital malformation of face NOSQ18
- •congenital malformation syndromes classified toQ87
- •dentofacial anomalies [including malocclusion]M26
- •musculoskeletal deformities of head and faceQ67.0-Q67.4
- skull defects associated with congenital anomalies of brain such as:
- •anencephalyQ00.0
- •encephaloceleQ01
- •hydrocephalusQ03
- •microcephalyQ02
Excludes 2
Conditions not included here, but the patient may have both
Related Codes(7)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(115)
SNOMED CT
- Crouzon craniofacial dysostosis28861008
- Crouzon syndrome28861008
- Crouzon's disease28861008
- Congenital anomaly of nasal bone93011006
- Temporo-aural dysostosis109397008
- Maxillary dysostosis109398003
- Maxillo-zygomatic dysostosis109399006
- Naso-maxillary dysostosis109400004
- Internasal dysostosis109407001
- Frontal dysostosis109408006
- Fronto-frontal dysostosis109410008
- Fronto-naso-ethmoidal dysostosis109411007
- Sphenoidal dysostosis109414004
- Spheno-frontal dysostosis109415003
- Dysostosis of bone of skull128219005
- Acanthosis nigricans402599005
- Fibroblast growth factor receptor 3 (FGFR3) related craniosynostosis440350001
- Fibroblast growth factor receptor 3-related craniosynostosis440350001
- Crouzon syndrome with acanthosis nigricans702361006
- Crouzonodermoskeletal syndrome702361006
- Acro-fronto-facio-nasal dysostosis720408003
- Acrofrontofacionasal dysostosis720408003
- Richieri Costa Colletto syndrome720408003
- Acrocraniofacial dysostosis720418008
- Kaplan Plauchu Fitch syndrome720418008
- Acrofacial dysostosis Catania type720419000
- Opitz Caltabiano syndrome720419000
- Acrofacial dysostosis Kennedy Teebi type720427009
- Kennedy Teebi syndrome720427009
- Acrofacial dysostosis Palagonia type720429007
- Acrofacial dysostosis Rodriguez type720430002
- Acro-fronto-facio-nasal dysostosis type 2721835008
- Acrofrontofacionasal dysostosis type 2721835008
- Hypertelorism, hypospadias, polysyndactyly syndrome721835008
- Naguib Richieri Costa syndrome721835008
- Hypomandibular faciocranial dysostosis721845005
UMLS
- Craniofacial DysarthrosesC0010273
- Craniofacial DysarthrosisC0010273
- Craniofacial DysostosesC0010273
- Craniofacial DysostosisC0010273
- Craniofacial Dysostosis SyndromeC0010273
- Craniofacial Dysostosis SyndromesC0010273
- Craniofacial dysarthrosisC0010273
- Craniofacial dysostosisC0010273
- Craniofacial dysostosis syndromeC0010273
- Crouzon SyndromeC0010273
- Crouzon craniofacial dysostosisC0010273
- Crouzon syndromeC0010273
- Crouzon syndrome (disorder)C0010273
- Crouzon's diseaseC0010273
- Dysarthroses, CraniofacialC0010273
- Dysarthrosis, CraniofacialC0010273
- Dysostoses, CraniofacialC0010273
- Dysostosis, CraniofacialC0010273
- craniofacial dysostosisC0010273
- crouzon diseaseC0010273
- crouzon syndromeC0010273
- crouzon's diseaseC0010273
- crouzon's syndromeC0010273
- crouzons diseaseC0010273
- crouzons syndromeC0010273
- syndrome craniofacial dysostosisC0010273
- syndrome crouzon'sC0010273
Clinical Terms
- crouzon's disease
- crouzon's syndrome
- crouzons syndrome
- Acrofacial dysostosis Rodriguez type
- Craniofacial Dysostosis Syndrome
- Internasal dysostosis
- Frontal dysostosis
- crouzons disease
- Fibroblast growth factor receptor 3-related craniosynostosis
- Fibroblast growth factor receptor 3 (FGFR3) related craniosynostosis
- Acro-fronto-facio-nasal dysostosis type 2
- syndrome crouzon's
- Sphenoidal dysostosis
- Acrocraniofacial dysostosis
- syndrome craniofacial dysostosis
- Acrofacial dysostosis Kennedy Teebi type
- Acrofacial dysostosis Catania type
- Naguib Richieri Costa syndrome
- Temporo-aural dysostosis
- Craniofacial Dysarthroses
- Craniofacial Dysostosis Syndromes
- Dysostoses, Craniofacial
- crouzon syndrome
- crouzon disease
- Acrofrontofacionasal dysostosis
- Fronto-frontal dysostosis
- Crouzon craniofacial dysostosis
- Crouzon syndrome (disorder)
- Hypertelorism, hypospadias, polysyndactyly syndrome
- Kennedy Teebi syndrome
- Dysarthroses, Craniofacial
- Dysarthrosis, Craniofacial
- Maxillo-zygomatic dysostosis
- Congenital anomaly of nasal bone
- Acro-fronto-facio-nasal dysostosis
- Acanthosis nigricans
- Richieri Costa Colletto syndrome
- Craniofacial Dysostoses
- Naso-maxillary dysostosis
- Craniofacial Dysarthrosis
- Dysostosis of bone of skull
- Acrofacial dysostosis Palagonia type
- Fronto-naso-ethmoidal dysostosis
- Dysostosis, Craniofacial
- Acrofrontofacionasal dysostosis type 2
- Hypomandibular faciocranial dysostosis
- Opitz Caltabiano syndrome
- Maxillary dysostosis
- Crouzon syndrome with acanthosis nigricans
- Spheno-frontal dysostosis
- Crouzonodermoskeletal syndrome
- Kaplan Plauchu Fitch syndrome
Frequently Asked Questions
What is the ICD-10 code for craniofacial dysostosis?
The ICD-10-CM code for craniofacial dysostosis is Q75.1. The full clinical description is "Craniofacial dysostosis". Q75.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q75.1 mean?
ICD-10-CM code Q75.1 represents “Craniofacial dysostosis”. 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 Q75.1 a billable code?
Yes, Q75.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q75.1 in?
Q75.1 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q75.1?
Q75.1 has Excludes1 notes indicating codes that cannot be used together with it, including: congenital malformation of face NOS (Q18.-); congenital malformation syndromes classified to Q87.-; dentofacial anomalies [including malocclusion] (M26.-); and 6 more.
What SNOMED CT codes does Q75.1 map to?
Q75.1 maps to 24 SNOMED CT concepts: 402599005, 720408003, 721835008, 720418008, 720419000, and 19 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q75.1?
Q75.1 is linked to 1 UMLS Concept Unique Identifier: C0010273. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does Q75.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like craniofacial dysostosis 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 Q75.1?
Q75.1 maps to the ICD-11 code: LD25.3 (Craniofacial dysostoses).
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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.