Q75.4

Billable

Mandibulofacial dysostosis

Mandibulofacial dysostosis

Status

Billable / Specific

Parent Code

Q75

ICD-11 Mapping

1 equivalent

Coding 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)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(7)
Q75.0

Craniosynostosis

Q75.1

Craniofacial dysostosis

BillableQ75.2

Hypertelorism

BillableQ75.3

Macrocephaly

BillableQ75.5

Oculomandibular dysostosis

BillableQ75.8

Oth congenital malformations of skull and face bones

BillableQ75.9

Congenital malformation of skull and face bones, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LD2F.16Otomandibular dysplasiaequivalentPrimary
Also Known As / Clinical Terms(136)

SNOMED CT

UMLS

Clinical Terms

  • Congenital asymmetry of mandible
  • Patterson Stevenson Fontaine syndrome
  • TCOF
  • Craniofacial microsomia
  • Eyes wide apart
  • Macroblepharon, ectropion, hypertelorism, macrostomia syndrome
  • X-linked mandibulofacial dysostosis
  • Mandibulofacial dysostosis with microcephaly
  • Franceschetti-Zwahlen-Klein Syndromes
  • Treacher-Collins' syndrome
  • Mandibulofacial dysostosis, macroblepharon, macrostomia syndrome
  • Treacher Collins-Franceschetti Syndrome
  • Sphenoidal dysostosis
  • treacher collins syndrome
  • Mandibulofacial dysostosis without limb anomalies
  • Orbital separation excessive
  • Mandibulofacial dysostosis Toriello type
  • First arch syndrome
  • Otomandibular dysostosis
  • Temporo-auro-mandibular dysostosis
  • MFD1
  • Hypertelorism
  • Syndrome, Franceschetti-Zwahlen-Klein
  • Otomandibular syndrome
  • Syndrome, Treacher Collins-Franceschetti
  • Mandibulofacial dysostosis, Guion-Almeida type
  • Split foot deformity with mandibulofacial dysostosis syndrome
  • Syndromes, Franceschetti-Zwahlen-Klein
  • Dysostosis, Mandibulofacial
  • Congenital asymmetry of jaw
  • Franceschetti-Zwahlen-Klein syndrome
  • MFDA - mandibulofacial dysostosis with alopecia
  • Mandibulofacial dysostosis with alopecia
  • Dysostoses, Mandibulofacial
  • Treacher-Collins Syndrome
  • Syndromes, Treacher Collins-Franceschetti
  • Asymmetry of mandible
  • TREACHER COLLINS SYNDROME 1
  • Intermandibular dysostosis
  • treacher collins' syndrome
  • berry syndrome
  • syndrome treacher collins
  • syndrome treacher collin
  • Franceschetti Zwahlen Klein Syndrome
  • collins syndrome treachers
  • TCS1
  • Mandibulofacial Dysostoses
  • Congenital mandibular asymmetry
  • TCS
  • Franceschetti syndrome
  • Treacher Collins-Franceschetti Syndromes
  • Syndrome, Treacher Collins
  • Orbital hypertelorism
  • treacher collin syndrome
  • Franceschetti Klein syndrome
  • collins syndrome treacher
  • Treacher Collins syndrome (disorder)
  • Congenital facial asymmetry
  • Franceschetti's syndrome
  • Eyes widely set
  • Treacher Collins Franceschetti Syndrome
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.

How does Q75.4 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like mandibulofacial 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 Q75.4?

Q75.4 maps to the ICD-11 code: LD2F.16 (Otomandibular dysplasia).

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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.