Q75.009
BillableCraniosynostosis unspecified
Craniosynostosis unspecified
Status
Billable / Specific
Parent Code
Q75.00Coding 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)
- 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
- Early fontanel closure1667003
- Dandy-Walker deformity14447001
- Dandy-Walker malformation14447001
- Dandy-Walker syndrome14447001
- Ambiguous genitalia21321009
- Imperfect fusion of skull23939000
- Acrocephaly48069004
- Egg-shaped skull48069004
- Elongated skull48069004
- Oxycephaly48069004
- Tower skull48069004
- Turricephaly48069004
- CSO - Craniosynostosis57219006
- Congenital ossification of cranial sutures57219006
- Congenital ossification of sutures of skull57219006
- Craniostenosis57219006
- Craniostosis57219006
- Craniosynostosis57219006
- Craniosynostosis syndrome57219006
- Premature closure of cranial sutures57219006
- Premature cranial suture closure57219006
- Acrocephalosyndactyly type 570410008
- Acrocephalosyndactyly type V70410008
- Pfeiffer syndrome70410008
- Pfeiffer-type acrocephalosyndactyly70410008
- Baller-Gerold syndrome77608001
- Craniosynostosis-radial aplasia syndrome77608001
- Frontonasal dysplasia sequence86610004
- Median cleft face syndrome86610004
- Lambdoid craniosynostosis109417006
- Parieto-occipital craniosynostosis109417006
- Congenital retrognathism109515000
- Retrognathia109515000
- Retrognathism109515000
- Marfanoid physique248298009
- Closure of fontanelle248382004
- Acrocephalosyndactyly268262006
- Recession of bone298358008
- Fibroblast growth factor receptor 3 (FGFR3) related craniosynostosis440350001
- Fibroblast growth factor receptor 3-related craniosynostosis440350001
- Camero Lituania Cohen syndrome715434005
- Genoa syndrome715434005
- Holoprosencephaly craniosynostosis syndrome715434005
- Spondyloepiphyseal dysplasia Nishimura type718766002
- Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome718766002
- Marfanoid craniosynostosis syndrome719069008
- Shprintzen Goldberg craniosynostosis syndrome719069008
- Shprintzen-Goldberg syndrome719069008
- CDAGS (craniosynostosis, clavicular hypoplasia, delayed closure of fontanelle, anal anomalies, genitourinary malformations, skin eruption) syndrome720812002
- CDAGS syndrome720812002
- Craniosynostosis, anal anomaly, porokeratosis syndrome720812002
- Braddock Jones Superneau syndrome720813007
- Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome720813007
- Craniosynostosis and intracranial calcification syndrome720816004
- Longman Tolmie syndrome720816004
- Craniosynostosis Boston type720817008
- Craniosynostosis Warman type720817008
- Warman Mulliken Hayward syndrome720817008
- Craniosynostosis Philadelphia type720818003
- Hunter McAlpine craniosynostosis syndrome721227001
- Gracile bone dysplasia722109008
- Osteocraniosplenic syndrome722109008
- Osteocraniostenosis722109008
- Osteosclerosis, developmental delay, craniosynostosis syndrome722117000
- Agammaglobulinaemia, microcephaly, craniosynostosis, severe dermatitis syndrome722281001
- Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome722281001
- Craniomicromelic syndrome725098001
- Craniosynostosis fibular aplasia syndrome732250002
- Lowry syndrome732250002
- SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome734173003
- SCARF syndrome734173003
- Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome734173003
- Craniosynostosis Herrmann Opitz type763684005
- Craniosynostosis and dental anomalies syndrome773332008
- Kreiborg Pakistani syndrome773332008
- Craniorhiny784350004
- Muenke syndrome787407003
- Agenesis of fibula1003546000
- Pfeiffer syndrome type 11003877009
- Pfeiffer syndrome type 21003916008
- Pfeiffer syndrome type 31003918009
- Congenital dysplasia of radius1142185008
- Aplasia of fibula1145459008
- Craniosynostosis, microretrognathia, severe intellectual disability syndrome1269224009
- Complex craniosynostosis8611000119100
- Simple craniosynostosis255581000119100
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.
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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.