Craniofacial microsomia
Isolated median cleft face syndrome
Reduced ossification of alisphenoid bone
Congenital fenestration of nasal bone
Congenital abnormal shape of nasal bone
Supraorbital facial cleft - Tessier cleft 11
Craniolenticulosutural dysplasia
Congenital absence of squamosal bone
Congenital small frontal bone
Increased basal angle of skull base
Reduced ossification of basisphenoid bone
Congenital abnormal fusion of vomer
RNF135 (ring finger protein 135) related overgrowth syndrome
Incomplete ossification of exoccipital bone
Congenital abnormal fusion of interparietal bone
Congenital hypoplasia of bone of cranium
Congenital small vomer
Congenital fenestration of parietal bone
COX - Cytochrome C oxidase deficiency
Reduced ossification of interparietal bone
Currarino idiopathic osteoarthropathy
Congenital abnormal fusion of basisphenoid bone
Reduced ossification of zygomatic bone
Agenesis of nasal bone
Posterior perimaxillary faciosynostosis
Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome
Frontorhiny
Congenital abnormal fusion of tympanic anulus
Scaphocephaly
Mitochondrial complex IV deficiency
Supraorbital facial cleft - Tessier cleft 9
Agenesis of vomer
Congenital small exoccipital bone
Unossified nasal bone
Congenital small alisphenoid bone
Congenital small basioccipital bone
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome
Congenital misshapen parietal bone
Congenital basisphenoid hole
Congenital abnormal fusion of premaxilla
Bilateral craniofacial microsomia
Overgrowth, macrocephaly, facial dysmorphism syndrome
Bathrocephaly
Congenital hypoplasia of carotid canal
Congenital abnormal fusion of zygomatic bone
Short stature, pituitary and cerebellar defect and small sella turcica syndrome
Acrocephalopolydactylous dysplasia
Congenital anomaly of alisphenoid bone
Congenital anomaly of presphenoid bone
Congenital anomaly of lacrimal bone
Burn McKeown syndrome
Cloverleaf skull syndrome
Hereditary cranium bifidum
Incomplete ossification of cranium
Poorly developed clavicle
Unossified basioccipital bone
Spheno-fronto-parietal craniofaciosynostosis
Interparietal craniosynostosis
Congenital abnormal fusion of supraoccipital bone
Congenital anomaly of squamosal bone
Incomplete ossification of palatine bone
Incomplete ossification of tympanic anulus
Congenital interparietal hole
Endosteal hyperostoses
Atresia of posterior naris
ALX3-related frontonasal dysplasia
Congenital misshapen presphenoid bone
Unossified zygomatic bone
Reduced ossification of exoccipital bone
Basilar skull invagination
Congenital fenestration of supraoccipital bone
Unossified presphenoid bone
Congenital small squamosal bone
Elejalde syndrome
Congenital anomaly of basisphenoid bone
Congenital hypoplasia of premaxilla
Aplasia of cranium
Complex IV deficiency
Congenital hypoplastic carotid canal
Pancreatic exocrine insufficiency
Congenital hypoplasia of both zygomatic bones
Congenital J shaped sella turcica
Doughnut lesion of calvaria and bone fragility syndrome
Unossified palatine bone
Cantu craniofaciofrontodigital syndrome
Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome
Reduced ossification of palatine bone
Bipartite ossification of interparietal bone
Lack of ossification of basisphenoid bone
Congenital parietal hole
Supraorbital facial cleft - Tessier cleft 13
Congenital misshapen vomer
Congenital abnormal shape of parietal bone
Congenital dyserythropoietic anemia
Congenital fused parietal bone
Cranio-cerebello-cardiac dysplasia syndrome
Congenital small nasal septum
Congenital hypoplasia of squamosal bone
X-linked intellectual disability, craniofacioskeletal syndrome
Congenital forehead deformity
Lacunar skull
Agenesis of tympanic anulus
Unossified alisphenoid bone
Congenital abnormality of skull shape
Agenesis of basioccipital bone
Richieri Costa Guion Almeida Ramos syndrome
Incomplete ossification of zygomatic bone
Supraorbital facial cleft - Tessier cleft 12
Paramedian facial cleft - Tessier cleft 3
Congenital misshapen premaxilla
Oblique facial cleft to upper lip AND upper jaw
Unossified tympanic anulus
Cleft mandible
Congenital small parietal bone
Congenital anomaly of parietal bone
Supraorbital facial cleft - Tessier cleft 8
Congenital basioccipital hole
Craniofacial cleft
Parietal foramina
Congenital frontal hole
Midline facial cleft - Tessier cleft 0
Lack of ossification of alisphenoid bone
Incomplete ossification of presphenoid bone
Orbital separation excessive
Congenital absence of basisphenoid bone
Congenital fenestration of exoccipital bone
Aplasia of nasal bone
Reduced ossification of tympanic anulus
Unossified parietal bone
Reduced ossification of supraoccipital bone
Lack of ossification of parietal bone
Congenital hypoplasia of frontal bone
Anterior perimaxillary faciosynostosis
Congenital abnormal shape of squamosal bone
Lack of ossification of frontal bone
Congenital abnormal fusion of basioccipital bone
Congenital fused squamosal bone
Congenital fenestration of squamosal bone
Congenital hypoplasia of interparietal bone
Complex craniosynostosis
Congenital absence of zygomatic bone
Congenital misshapen supraoccipital bone
Congenital hypoplasia of lacrimal bone
Paramedian facial cleft - Tessier cleft 2
Agenesis of frontal bone
Choanal atresia
ALX homeobox 3-related frontonasal dysplasia
Reduced ossification of presphenoid bone
Unossified frontal bone
Congenital small premaxilla
Microbrachycephaly, ptosis, cleft lip syndrome
Unossified interparietal bone
Incomplete ossification of alisphenoid bone
Impression, Basilar
MacDermot Winter syndrome
Congenital hypertrophy of sphenoid bone
Obtuse basal angle of skull base
Congenital absence of skull bone (disorder)
Congenital abnormal shape of basioccipital bone
Reduced ossification of basioccipital bone
Craniofacial dysplasia osteopenia syndrome
Craniofenestria
Wormian bone of cranium
Vomero-premaxillary faciosynostosis
Aplasia of bone of cranium
Incomplete ossification of nasal bone
Localized congenital skull defect
Craniofacial conodysplasia syndrome
Congenital misshapen alisphenoid bone
Congenital absence of nasal bone
Frontonasal dysplasia
Congenital abnormal shape of exoccipital bone
Robin sequence with cleft mandible and limb anomalies syndrome
Congenital deformity of forehead
Infraorbital facial cleft - Tessier cleft 5
Congenital hypoplasia of nasal septum
Prominent glabella with microcephaly and hypogenitalism syndrome
Congenital anomaly of vomer
platybasia
Bipartite ossification
Congenital absence of skull bone
Familial doughnut lesions of skull
Agenesis of basisphenoid bone
Lack of ossification of premaxilla
Absence of skull bone, congenital
Congenital fused presphenoid bone
Congenital small zygomatic bone
Congenital absence of nasal bones
Congenital atresia of posterior nares
Congenital abnormal shape of premaxilla
Congenital enlargement of fontanel
Stratton Parker syndrome
Congenital absence of supraoccipital bone
Hypertelorism
Unossified supraoccipital bone
Midline cleft syndrome
Cranium bifidum
Acrania
Calvarial doughnut lesion with bone fragility syndrome
Congenital abnormal fusion of presphenoid bone
Congenital fenestration of alisphenoid bone
Congenital anomaly of zygomatic bone
Congenital absence of cranial vault
Boyadjiev Jabs syndrome
Congenital small presphenoid bone
Frontonasal dysplasia sequence
Congenital fenestration of premaxilla
Congenital hypoplasia of basioccipital bone
Congenital fused interparietal bone
Congenital abnormal fusion of squamosal bone
Lack of ossification of supraoccipital bone
Congenital absence of tympanic anulus
Reduced ossification of nasal bone
Flattening of the skull base
Congenital abnormal shape of supraoccipital bone
Congenital abnormal shape of presphenoid bone
Congenital fused alisphenoid bone
Incomplete ossification of parietal bone
Leptocephaly
Congenital absence of premaxilla
Unossified basisphenoid bone
Congenital fused zygomatic bone
Congenital hypoplasia of alisphenoid bone
Congenital presphenoid hole
Congenital anomaly of sphenoid wing
Cytochrome-c oxidase deficiency
Congenital abnormal shape of tympanic anulus
Bifid ossification
Frontosphenoidal dysplasia
Congenital exoccipital hole
Congenital malformation of anterior pituitary
Lack of ossification of interparietal bone
Congenital hypoplasia of adenohypophysis
Hyperostosis cranialis interna
Congenital facial asymmetry
Congenital fused tympanic anulus
Sagittal synostosis
Cranioosteoarthropathy
Congenital absence of frontal bone
Congenital misshapen tympanic anulus
Osteosclerosis
Basilar Impression
Congenital absence of parietal bone
Congenital anomaly of anterior pituitary
Congenital misshapen frontal bone
Platybasia (disorder)
Median cleft face syndrome
Unossified squamosal bone
Agenesis of neurocranium
Congenital absence of vomer
Pancreatic insufficiency
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome
Reginato Schiapachasse syndrome
Congenital abnormal shape of vomer
Symmetric parietal foramina
CDA - congenital dyserythropoietic anemia
Lack of ossification of nasal bone
Congenital misshapen zygomatic bone
Congenital abnormal fusion of exoccipital bone
Agenesis of alisphenoid bone
Prominent frontal ridges
Eyes wide apart
Aplasia of premaxilla
Bossed forehead
Frontal bossing
Bifid ossification of supraoccipital bone
Congenital hypoplasia of parietal bone
Bifid ossification of interparietal bone
Congenital hypoplasia of anterior pituitary
Congenital absence of exoccipital bone
Congenital hypoplasia of bone of skull
Incomplete ossification of supraoccipital bone
Supraorbital facial cleft - Tessier cleft 10
Congenital fused premaxilla
Incomplete ossification of skull
Congenital nasal bone hole
Ritscher Schinzel syndrome
Lack of ossification of tympanic anulus
Infraorbital facial cleft - Tessier cleft 6
Agenesis of presphenoid bone
Congenital squamosal hole
Catlin marks
Agenesis of squamosal bone
Anterior pituitary hormone deficiency
Enlarged parietal foramina
Orbital hypertelorism
Congenital absence of alisphenoid bone
Congenital abnormal shape of basisphenoid bone
Split lower lip and mandible
Congenital fenestration of basisphenoid bone
Congenital fused supraoccipital bone
Congenital absence of nasal septum
Acrocephalopolydactyly
Frontal dysostosis
Congenital anomaly of palatine bone
Congenital misshapen basioccipital bone
Midline facial cleft - Tessier cleft 14
Pancreatic insufficiency, dyserythropoietic anaemia, calvarial hyperostosis syndrome
Infraorbital facial cleft - Tessier cleft 7
Craniolacunia
Occipital dysplasia
Lack of ossification of basioccipital bone
Reduced ossification of squamosal bone
Mandibular cleft
Impressions, Basilar
EPI - exocrine pancreatic insufficiency
SIX2-related frontonasal dysplasia
Cranio-osteoarthropathy
Domed head
Basilar Impressions
Congenital anomaly of supraoccipital bone
Congenital anomaly of exoccipital bone
Congenital fenestration of presphenoid bone
Lack of ossification of zygomatic bone
Paramedian facial cleft - Tessier cleft 1
Congenital alisphenoid hole
Congenital anomaly of basioccipital bone
Cranial aplasia
Cytochrome c oxidase deficiency
Cloverleaf skull with multiple congenital anomalies syndrome
Aplasia of bone of skull
Incomplete ossification of premaxilla
Midline facial cleft - Tessier cleft 30
Short stature, wormian bones, dextrocardia syndrome
Congenital deformity of forehead (disorder)
Lack of ossification of palatine bone
Congenital small interparietal bone
CDA - congenital dyserythropoietic anaemia
Hypoplastic clavicle
Congenital hypoplasia of left zygomatic bone
Congenital fenestration of frontal bone
Craniofaciofrontodigital syndrome
3C syndrome
Incomplete ossification of basioccipital bone
Delayed membranous cranial ossification
Defect of skull ossification
Congenital misshapen squamosal bone
SIX homeobox 2-related frontonasal dysplasia
Congenital fused vomer
Congenital fenestration of interparietal bone
Congenital fused frontal bone
Congenital malformation of sphenoid wing
Agenesis of premaxillary bone
Congenital small clavicle
Pierre Robin syndrome
Cranioschisis
Congenital hypoplasia of clavicle
Reduced ossification of parietal bone
Reduced ossification of premaxilla
Agenesis of zygomatic bone
Congenital abnormal fusion of frontal bone
Congenital abnormal shape of alisphenoid bone
Congenital anomaly of premaxilla
Platybasias
Incomplete ossification of basisphenoid bone
Congenital small basisphenoid bone
Lack of ossification of exoccipital bone
Agenesis of interparietal bone
Agenesis of supraoccipital bone
Congenital fenestration of basioccipital bone
Congenital anomaly of interparietal bone
Currarino disease
Congenital abnormal shape of frontal bone
Congenital absence of presphenoid bone
Lack of ossification of presphenoid bone
Complete perimaxillary faciosynostosis
Craniocerebellocardiac dysplasia
Richieri Costa Pereira syndrome
Cranial hypoplasia
Parietal foramina with cleidocranial dysplasia
Ring finger protein 135 related overgrowth syndrome
Congenital anomaly of tympanic anulus
Incomplete ossification of interparietal bone
Agenesis of exoccipital bone
Agenesis of premaxilla
Congenital abnormal shape of zygomatic bone
Flat base of skull
Incomplete ossification of frontal bone
Congenital asymmetry of forehead
Parieto-occipital craniosynostosis
Reduced ossification of frontal bone
Congenital absence of interparietal bone
Congenital dyserythropoietic anaemia
Kleeblattschadel deformity
Disorder of lacrimal bone
Robin sequence
Congenital atresia of choana
Congenital anomaly of nasal bone
Exocrine pancreatic insufficiency
Congenital fused basioccipital bone
Hamamy syndrome
Congenital misshapen nasal bone
Atresia of posterior nares
Congenital abnormal fusion of alisphenoid bone
Congenital hypoplasia of supraoccipital bone
Infraorbital facial cleft - Tessier cleft 4
Eyes widely set
Unossified exoccipital bone
Congenital small supraoccipital bone
Congenital fused basisphenoid bone
Congenital supraoccipital hole
Localised congenital skull defect
Clover leaf skull deformity
Congenital hypoplasia of bilateral zygomatic bones
Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome
Congenital premaxilla hole
Bipartite ossification of supraoccipital bone
Congenital hypoplasia of zygomatic bone
Congenital hypoplasia of exoccipital bone
Lambdoid craniosynostosis
Sagittal craniosynostosis
Congenital small tympanic anulus
Congenital misshapen basisphenoid bone
Lückenschädel
Congenital anomaly of craniovertebral junction
Lack of ossification of squamosal bone
Pierre Robin association
Incomplete ossification of squamosal bone
Congenital abnormal fusion of parietal bone
Congenital misshapen interparietal bone
Parietal foramina with clavicular hypoplasia
Overriding skull bones
Cheilognathoprosoposchisis
Frontonasal dysplasia type 1
Congenital hypoplasia of vomer
Congenital hypoplasia of right zygomatic bone
Congenital fused exoccipital bone
Congenital hypoplasia of tympanic anulus
Leptocephalus
Congenital hypoplasia of basisphenoid bone
Congenital anomaly of frontal bone
Congenital absence of basioccipital bone
Congenital hypoplasia of presphenoid bone
Metopic ridging, ptosis, facial dysmorphism syndrome
Absence of skull bone
Gonzales-del Angel syndrome
Congenital enlarged fontanel
Micrognathia-glossoptosis syndrome
Unossified premaxilla
Congenital misshapen exoccipital bone
Congenital abnormal shape of interparietal bone
Agenesis of parietal bone
Prosoposchisis
Congenital small lacrimal bone

Frequently Asked Questions

What is the ICD-10 code for oth congenital malformations of skull and face bones?

The ICD-10-CM code for oth congenital malformations of skull and face bones is Q75.8. The full clinical description is "Other specified congenital malformations of skull and face bones". Q75.8 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q75.8 mean?

ICD-10-CM code Q75.8 represents “Other specified congenital malformations of skull and face bones”. 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 Q75.8 a billable code?

Yes, Q75.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q75.8 in?

Q75.8 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q75.8?

Q75.8 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 Q75.8 map to?

Q75.8 maps to 234 SNOMED CT concepts: 718556007, 1230021007, 275349007, 203923004, 720417003, and 229 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q75.8?

Q75.8 is linked to 4 UMLS Concept Unique Identifiers: C2937218, C0032209, C0265533, C0478073. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q75.8 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like oth congenital malformations of skull and face bones 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 Q75.8?

Q75.8 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.