Q75.9
BillableCongenital malformation of skull and face bones, unspecified
Congenital malformation of skull and face bones, unspecified
Status
Billable / Specific
Parent Code
Q75Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital anomaly of face bones NOS
- Congenital anomaly of skull NOS
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
- Brachycephaly13649004
- Short anteroposterior diameter of skull13649004
- Short broad skull13649004
- Wide skull13649004
- CDH - Congenital diaphragmatic hernia17190001
- Congenital diaphragmatic hernia17190001
- Congenital dilatation of colon24291004
- Congenital megacolon24291004
- Congenital anomaly of face bones32003007
- Face congenital deformities32003007
- Congenital anomaly of skull51655004
- Congenital skull malformation51655004
- Athetoid cerebral palsy75019001
- Congenital anomaly of head87290003
- Congenital anomaly of alisphenoid bone92992008
- Congenital anomaly of basisphenoid bone92996006
- Congenital anomaly of fetal head bones93003001
- Congenital anomaly of foetal head bones93003001
- Congenital anomaly of supraoccipital bone93026008
- Interparietal craniosynostosis109418001
- Sagittal craniosynostosis109418001
- Sagittal synostosis109418001
- Scaphocephaly109418001
- Dyskinetic cerebral palsy230780007
- Skull congenital deformities253979005
- Craniofacial microsomia254026007
- Congenital abnormality of skull and face bones268239009
- Skull and face bone anomalies268239009
- Localised congenital skull defect270519009
- Localized congenital skull defect270519009
- Congenital anomaly of sphenoid wing431768007
- Congenital malformation of sphenoid wing431768007
- Congenital hernia of foramen of Bochdalek447821002
- Congenital posterolateral diaphragmatic hernia447821002
- Pleuroperitoneal hernia447821002
- Extrapyramidal cerebral palsy702314005
- Non-spastic cerebral palsy702314005
- Craniofacial deafness hand syndrome702362004
- Sommer Young Wee Frye syndrome702362004
- Haspeslagh Fryns Muelenaere syndrome716090004
- Short stature with craniofacial anomalies and genital hypoplasia syndrome716090004
- Deafness craniofacial syndrome716245003
- Cardiocranial syndrome Pfeiffer type720606005
- Craniosynostosis with congenital heart disease and intellectual disability syndrome720606005
- Pfeiffer Singer Zschiesche syndrome720606005
- Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis720606005
- Diaphragmatic defect, limb deficiency, skull defect syndrome721095007
- Froster Huch syndrome721095007
- Al Gazali Donnai Muller syndrome721223002
- Hirschsprung disease with nail hypoplasia and dysmorphism721223002
- Mitochondrial DNA depletion syndrome encephalomyopathic form765401006
- Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form765401006
- Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome783005002
- OAV (oculo-auriculo-vertebral) spectrum1010685005
- Oculo-auriculo-vertebral spectrum1010685005
- Oculoauriculovertebral spectrum1010685005
- Congenital hypoplasia of nail unit1144442009
- Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, deafness syndrome1187039001
- Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome1187039001
- Hyaluronidase 2 deficiency1187039001
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies1208937004
- Mitochondrial deoxyribonucleic acid depletion syndrome, encephalomyopathic form with variable craniofacial anomalies1208937004
- mtDNA (mitochondrial deoxyribonucleic acid) depletion syndrome, encephalomyopathic form with variable craniofacial anomalies1208937004
- Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome1217229007
- Developmental delay, short stature, dysmorphic features, sparse hair syndrome1217229007
- Loucks Innes syndrome1217229007
- Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome1217382002
- Pilarowski Bjornsson syndrome1217382002
- Au Kline syndrome1222710008
- Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome1222710008
- Okamoto syndrome1222710008
- Arboleda Tham syndrome1255319004
- Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome1255319004
- Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1-4 mutation1304277005
- Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation1304277005
- H1-4-related neurodevelopmental disorder1304277005
- Rahman syndrome1304277005
- Body height below reference range1363478003
- Congenital facial asymmetry13851000119109
UMLS
- Congenital abnormality of skull and face bonesC0495615
- Congenital abnormality of skull and face bones (disorder)C0495615
- Congenital malformation of skull and face bones, unspecifiedC0495615
- Skull and face bone anomaliesC0495615
- Congenital anomaly of face bonesC0265543
- Congenital anomaly of face bones (disorder)C0265543
- Congenital anomaly of face bones NOSC0265543
- Congenital anomaly of skullC0265527
- Congenital anomaly of skull (disorder)C0265527
- Congenital anomaly of skull NOSC0265527
- Congenital skull malformationC0265527
- Congenital skull malformation NOSC0265527
- Skull anomaliesC0265527
- Skull congenital deformitiesC0265527
- Skull congenital deformities (disorder)C0265527
- congenital cranial defectC0265527
Frequently Asked Questions
What is the ICD-10 code for congenital malformation of skull and face bones, unspecified?
The ICD-10-CM code for congenital malformation of skull and face bones, unspecified is Q75.9. The full clinical description is "Congenital malformation of skull and face bones, unspecified". Q75.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q75.9 mean?
ICD-10-CM code Q75.9 represents "Congenital malformation of skull and face bones, 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 Q75.9 a billable code?
Yes, Q75.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q75.9 in?
Q75.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q75.9?
Q75.9 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 Q75.9 map to?
Q75.9 maps to 39 SNOMED CT concepts: 721223002, 1255319004, 75019001, 1222710008, 1304277005, and 34 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q75.9?
Q75.9 is linked to 3 UMLS Concept Unique Identifiers: C0495615, C0265543, C0265527. 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.