Q75.1
BillableCraniofacial dysostosis
Craniofacial dysostosis
Status
Billable / Specific
Parent Code
Q75Coding 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 NOS (Q18.-)
- congenital malformation syndromes classified to Q87.-
- dentofacial anomalies [including malocclusion] (M26.-)
- musculoskeletal deformities of head and face (Q67.0-Q67.4)
- skull defects associated with congenital anomalies of brain such as:
- anencephaly (Q00.0)
- encephalocele (Q01.-)
- hydrocephalus (Q03.-)
- microcephaly (Q02)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
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
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.
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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.