Arboleda Tham syndrome
Congenital anomaly of face bones NOS
Craniofacial microsomia
Sagittal synostosis
Au Kline syndrome
Pleuroperitoneal hernia
H1-4-related neurodevelopmental disorder
Brachycephaly
Mitochondrial deoxyribonucleic acid depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
congenital cranial defect
Oculo-auriculo-vertebral spectrum
Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome
Mitochondrial DNA depletion syndrome encephalomyopathic form
Non-spastic cerebral palsy
Developmental delay, short stature, dysmorphic features, sparse hair syndrome
Congenital anomaly of foetal head bones
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome
Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome
Hirschsprung disease with nail hypoplasia and dysmorphism
OAV (oculo-auriculo-vertebral) spectrum
Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation
Scaphocephaly
Al Gazali Donnai Muller syndrome
Congenital skull malformation NOS
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
Skull anomalies
Congenital megacolon
Congenital anomaly of skull (disorder)
Okamoto syndrome
Short anteroposterior diameter of skull
Froster Huch syndrome
Congenital anomaly of skull NOS
Hyaluronidase 2 deficiency
Loucks Innes syndrome
Congenital anomaly of alisphenoid bone
Localized congenital skull defect
Deafness craniofacial syndrome
Craniofacial deafness hand syndrome
Congenital hernia of foramen of Bochdalek
Congenital posterolateral diaphragmatic hernia
Congenital anomaly of face bones (disorder)
Short broad skull
Interparietal craniosynostosis
Pfeiffer Singer Zschiesche syndrome
Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, deafness syndrome
Diaphragmatic defect, limb deficiency, skull defect syndrome
Wide skull
Congenital hypoplasia of nail unit
Congenital skull malformation
Pilarowski Bjornsson syndrome
Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome
Skull congenital deformities
Localised congenital skull defect
Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis
Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form
Body height below reference range
Sagittal craniosynostosis
Congenital anomaly of basisphenoid bone
Congenital anomaly of skull
Congenital anomaly of supraoccipital bone
Rahman syndrome
Congenital anomaly of fetal head bones
Sommer Young Wee Frye syndrome
Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome
Craniosynostosis with congenital heart disease and intellectual disability syndrome
Congenital abnormality of skull and face bones
Dyskinetic cerebral palsy
Cardiocranial syndrome Pfeiffer type
Congenital abnormality of skull and face bones (disorder)
mtDNA (mitochondrial deoxyribonucleic acid) depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
Congenital anomaly of face bones
Congenital anomaly of head
Face congenital deformities
Extrapyramidal cerebral palsy
Short stature with craniofacial anomalies and genital hypoplasia syndrome
Skull and face bone anomalies
Athetoid cerebral palsy
Congenital malformation of sphenoid wing
CDH - Congenital diaphragmatic hernia
Congenital anomaly of sphenoid wing
Congenital diaphragmatic hernia
Oculoauriculovertebral spectrum
Skull congenital deformities (disorder)
Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome
Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1-4 mutation
Haspeslagh Fryns Muelenaere syndrome
Congenital dilatation of colon
Congenital facial asymmetry

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.

How does Q75.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of skull and face bones, 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 Q75.9?

Q75.9 maps to the ICD-11 code: LB70.Z (Structural developmental anomalies of cranium, unspecified).

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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.