Q75.009

Billable

Craniosynostosis unspecified

Craniosynostosis unspecified

Status

Billable / Specific

Parent Code

Q75.00

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Imperfect fusion of skull

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(2)
Q75.001

Craniosynostosis unspecified, unilateral

BillableQ75.002

Craniosynostosis unspecified, bilateral

Billable
Also Known As / Clinical Terms(177)

SNOMED CT

UMLS

Clinical Terms

  • Osteocraniosplenic syndrome
  • Lowry syndrome
  • Pfeiffer syndrome type 1
  • Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
  • Premature cranial suture closure
  • Pfeiffer syndrome
  • Marfanoid physique
  • Craniostosis
  • Pfeiffer-type acrocephalosyndactyly
  • Craniosynostosis fibular aplasia syndrome
  • Retrognathia
  • Genoa syndrome
  • Median cleft face syndrome
  • Longman Tolmie syndrome
  • Warman Mulliken Hayward syndrome
  • Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome
  • Imperfect fusion of skull
  • Craniosynostosis and intracranial calcification syndrome
  • Tower skull
  • Egg-shaped skull
  • Acrocephaly
  • Camero Lituania Cohen syndrome
  • Closure of fontanelle
  • Shprintzen Goldberg craniosynostosis syndrome
  • Oxycephaly
  • Aplasia of fibula
  • Complex craniosynostosis
  • Craniosynostosis
  • Muenke syndrome
  • Fibroblast growth factor receptor 3-related craniosynostosis
  • Fibroblast growth factor receptor 3 (FGFR3) related craniosynostosis
  • Hunter McAlpine craniosynostosis syndrome
  • Congenital ossification of sutures of skull
  • Parieto-occipital craniosynostosis
  • Turricephaly
  • CDAGS (craniosynostosis, clavicular hypoplasia, delayed closure of fontanelle, anal anomalies, genitourinary malformations, skin eruption) syndrome
  • Acrocephalosyndactyly type 5
  • Holoprosencephaly craniosynostosis syndrome
  • Congenital dysplasia of radius
  • Pfeiffer syndrome type 2
  • Craniomicromelic syndrome
  • Gracile bone dysplasia
  • Osteocraniostenosis
  • Craniosynostosis and dental anomalies syndrome
  • CDAGS syndrome
  • Craniosynostosis Philadelphia type
  • Pfeiffer syndrome type 3
  • Osteosclerosis, developmental delay, craniosynostosis syndrome
  • Recession of bone
  • Ambiguous genitalia
  • Acrocephalosyndactyly
  • Craniosynostosis syndrome
  • Retrognathism
  • Lambdoid craniosynostosis
  • Congenital ossification of cranial sutures
  • Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome
  • Dandy-Walker malformation
  • Craniosynostosis, unspecified
  • SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome
  • Craniosynostosis Boston type
  • Craniostenosis
  • Agenesis of fibula
  • Dandy-Walker deformity
  • Elongated skull
  • Craniosynostosis, anal anomaly, porokeratosis syndrome
  • Premature closure of cranial sutures
  • SCARF syndrome
  • Braddock Jones Superneau syndrome
  • Frontonasal dysplasia sequence
  • Kreiborg Pakistani syndrome
  • Congenital retrognathism
  • Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome
  • Simple craniosynostosis
  • Baller-Gerold syndrome
  • Early fontanel closure
  • Acrocephalosyndactyly type V
  • Spondyloepiphyseal dysplasia Nishimura type
  • Craniorhiny
  • Imperfect fusion of skull (disorder)
  • Craniosynostosis Warman type
  • Dandy-Walker syndrome
  • Craniosynostosis-radial aplasia syndrome
  • CSO - Craniosynostosis
  • Craniosynostosis, microretrognathia, severe intellectual disability syndrome
  • Craniosynostosis Herrmann Opitz type
  • Marfanoid craniosynostosis syndrome
  • Shprintzen-Goldberg syndrome
  • Agammaglobulinaemia, microcephaly, craniosynostosis, severe dermatitis syndrome
Frequently Asked Questions
What is the ICD-10 code for craniosynostosis unspecified?

The ICD-10-CM code for craniosynostosis unspecified is Q75.009. The full clinical description is "Craniosynostosis unspecified". Q75.009 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q75.009 mean?

ICD-10-CM code Q75.009 represents “Craniosynostosis unspecified”. 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 Q75.009 a billable code?

Yes, Q75.009 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q75.009 in?

Q75.009 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q75.009?

Q75.009 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 Q75.009 map to?

Q75.009 maps to 44 SNOMED CT concepts: 268262006, 70410008, 48069004, 722281001, 1003546000, and 39 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q75.009?

Q75.009 is linked to 2 UMLS Concept Unique Identifiers: C5781050, C0265536. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q75.009 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like craniosynostosis unspecified 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 Q75.009?

There is no direct ICD-11 mapping available for Q75.009 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.