Q75.4
BillableMandibulofacial dysostosis
Mandibulofacial dysostosis
Status
Billable / Specific
Parent Code
Q75Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Franceschetti syndrome
- Treacher Collins syndrome
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
- First arch syndrome15557005
- Eyes wide apart22006008
- Eyes widely set22006008
- Hypertelorism22006008
- Orbital hypertelorism22006008
- Orbital separation excessive22006008
- Franceschetti Klein syndrome82203000
- Mandibulofacial dysostosis82203000
- Mandibulofacial dysostosis without limb anomalies82203000
- Treacher Collins syndrome82203000
- Congenital asymmetry of jaw90693008
- Otomandibular dysostosis109393007
- Otomandibular syndrome109393007
- Intermandibular dysostosis109394001
- Temporo-auro-mandibular dysostosis109395000
- Sphenoidal dysostosis109414004
- Congenital asymmetry of mandible109513007
- Congenital mandibular asymmetry109513007
- Asymmetry of mandible235082006
- Craniofacial microsomia254026007
- Mandibulofacial dysostosis with microcephaly711543008
- Mandibulofacial dysostosis, Guion-Almeida type711543008
- Mandibulofacial dysostosis Toriello type719813003
- X-linked mandibulofacial dysostosis719813003
- Patterson Stevenson Fontaine syndrome724069009
- Split foot deformity with mandibulofacial dysostosis syndrome724069009
- Macroblepharon, ectropion, hypertelorism, macrostomia syndrome773557002
- Mandibulofacial dysostosis, macroblepharon, macrostomia syndrome773557002
- MFDA - mandibulofacial dysostosis with alopecia1216943004
- Mandibulofacial dysostosis with alopecia1216943004
- Congenital facial asymmetry13851000119109
UMLS
- Dysostoses, MandibulofacialC0242387
- Dysostosis, MandibulofacialC0242387
- Franceschetti Klein syndromeC0242387
- Franceschetti Zwahlen Klein SyndromeC0242387
- Franceschetti syndromeC0242387
- Franceschetti's syndromeC0242387
- Franceschetti-Zwahlen-Klein SyndromeC0242387
- Franceschetti-Zwahlen-Klein SyndromesC0242387
- Franceschetti-Zwahlen-Klein syndromeC0242387
- MANDIBULOFACIAL DYSOSTOSISC0242387
- MFD1C0242387
- Mandibulofacial DysostosesC0242387
- Mandibulofacial DysostosisC0242387
- Mandibulofacial dysostosisC0242387
- Mandibulofacial dysostosis without limb anomaliesC0242387
- Syndrome, Franceschetti-Zwahlen-KleinC0242387
- Syndrome, Treacher CollinsC0242387
- Syndrome, Treacher Collins-FranceschettiC0242387
- Syndromes, Franceschetti-Zwahlen-KleinC0242387
- Syndromes, Treacher Collins-FranceschettiC0242387
- TCOFC0242387
- TCSC0242387
- TCS1C0242387
- TREACHER COLLINS SYNDROMEC0242387
- TREACHER COLLINS SYNDROME 1C0242387
- TREACHER COLLINS-FRANCESCHETTI SYNDROMEC0242387
- Treacher Collins Franceschetti SyndromeC0242387
- Treacher Collins SyndromeC0242387
- Treacher Collins syndromeC0242387
- Treacher Collins syndrome (disorder)C0242387
- Treacher Collins-Franceschetti SyndromeC0242387
- Treacher Collins-Franceschetti SyndromesC0242387
- Treacher Collins-Franceschetti syndromeC0242387
- Treacher-Collins SyndromeC0242387
- Treacher-Collins' syndromeC0242387
- berry syndromeC0242387
- collins syndrome treacherC0242387
- collins syndrome treachersC0242387
- mandibulofacial dysostosisC0242387
- syndrome treacher collinC0242387
- syndrome treacher collinsC0242387
- treacher collin syndromeC0242387
- treacher collins syndromeC0242387
- treacher collins' syndromeC0242387
Frequently Asked Questions
What is the ICD-10 code for mandibulofacial dysostosis?
The ICD-10-CM code for mandibulofacial dysostosis is Q75.4. The full clinical description is "Mandibulofacial dysostosis". Q75.4 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q75.4 mean?
ICD-10-CM code Q75.4 represents "Mandibulofacial 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 Q75.4 a billable code?
Yes, Q75.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q75.4 in?
Q75.4 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q75.4?
Q75.4 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 Q75.4 map to?
Q75.4 maps to 17 SNOMED CT concepts: 235082006, 90693008, 109513007, 13851000119109, 254026007, and 12 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q75.4?
Q75.4 is linked to 1 UMLS Concept Unique Identifier: C0242387. 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.