Diagnosis Code

Q75.8 OTH CONGENITAL MALFORMATIONS OF SKULL AND FACE BONES


Code Information

Diagnosis Code: Q75.8

Short Description: Oth congenital malformations of skull and face bones

Long Description: Other specified congenital malformations of skull and face bones

The code Q75.8 is VALID for claim submission

Code Classification:

  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Congenital malformations and deformations of the musculoskeletal system (Q65-Q79)
      • Other congenital malformations of skull and face bones (Q75)
        • Q75.8 Oth congenital malformations of skull and face bones

Code Version: 2022 ICD-10-CM


Synonyms

  • 3C syndrome
  • Absence of skull bone
  • Acrania
  • Acrania
  • Acrania
  • Acrocephalopolydactyly
  • Agenesis of nasal bone
  • Agenesis of premaxilla
  • Agenesis of vomer
  • Anterior perimaxillary faciosynostosis
  • Anterior pituitary hormone deficiency
  • Basilar skull invagination
  • Bathrocephaly
  • Bilateral craniofacial microsomia
  • Bipartite ossification
  • Bipartite ossification
  • Bipartite ossification of interparietal bone
  • Bipartite ossification of supraoccipital bone
  • Cheilognathoprosoposchisis
  • Choanal atresia
  • Choanal atresia, hearing loss, cardiac defect, craniofacial dysmorphism syndrome
  • Cleft mandible
  • Cloverleaf skull syndrome
  • Cloverleaf skull with multiple congenital anomalies syndrome
  • Complete perimaxillary faciosynostosis
  • Complex craniosynostosis
  • Complex craniosynostosis
  • Congenital abnormal fusion of alisphenoid bone
  • Congenital abnormal fusion of basioccipital bone
  • Congenital abnormal fusion of basisphenoid bone
  • Congenital abnormal fusion of exoccipital bone
  • Congenital abnormal fusion of frontal bone
  • Congenital abnormal fusion of interparietal bone
  • Congenital abnormal fusion of nasal bone
  • Congenital abnormal fusion of parietal bone
  • Congenital abnormal fusion of premaxilla
  • Congenital abnormal fusion of presphenoid bone
  • Congenital abnormal fusion of squamosal bone
  • Congenital abnormal fusion of supraoccipital bone
  • Congenital abnormal fusion of tympanic anulus
  • Congenital abnormal fusion of vomer
  • Congenital abnormal fusion of zygomatic bone
  • Congenital abnormal shape of alisphenoid bone
  • Congenital abnormal shape of basioccipital bone
  • Congenital abnormal shape of basisphenoid bone
  • Congenital abnormal shape of exoccipital bone
  • Congenital abnormal shape of frontal bone
  • Congenital abnormal shape of interparietal bone
  • Congenital abnormal shape of nasal bone
  • Congenital abnormal shape of parietal bone
  • Congenital abnormal shape of premaxilla
  • Congenital abnormal shape of presphenoid bone
  • Congenital abnormal shape of squamosal bone
  • Congenital abnormal shape of supraoccipital bone
  • Congenital abnormal shape of tympanic anulus
  • Congenital abnormal shape of vomer
  • Congenital abnormal shape of zygomatic bone
  • Congenital abnormality of skull shape
  • Congenital absence of alisphenoid bone
  • Congenital absence of basioccipital bone
  • Congenital absence of basisphenoid bone
  • Congenital absence of cranial vault
  • Congenital absence of exoccipital bone
  • Congenital absence of frontal bone
  • Congenital absence of interparietal bone
  • Congenital absence of nasal bone
  • Congenital absence of nasal septum
  • Congenital absence of nasal septum
  • Congenital absence of parietal bone
  • Congenital absence of premaxilla
  • Congenital absence of presphenoid bone
  • Congenital absence of skull bone
  • Congenital absence of squamosal bone
  • Congenital absence of supraoccipital bone
  • Congenital absence of tympanic anulus
  • Congenital absence of vomer
  • Congenital absence of zygomatic bone
  • Congenital anomaly of alisphenoid bone
  • Congenital anomaly of alisphenoid bone
  • Congenital anomaly of alisphenoid bone
  • Congenital anomaly of alisphenoid bone
  • Congenital anomaly of alisphenoid bone
  • Congenital anomaly of alisphenoid bone
  • Congenital anomaly of alisphenoid bone
  • Congenital anomaly of basioccipital bone
  • Congenital anomaly of basisphenoid bone
  • Congenital anomaly of basisphenoid bone
  • Congenital anomaly of basisphenoid bone
  • Congenital anomaly of basisphenoid bone
  • Congenital anomaly of basisphenoid bone
  • Congenital anomaly of basisphenoid bone
  • Congenital anomaly of basisphenoid bone
  • Congenital anomaly of craniovertebral junction
  • Congenital anomaly of exoccipital bone
  • Congenital anomaly of frontal bone
  • Congenital anomaly of interparietal bone
  • Congenital anomaly of lacrimal bone
  • Congenital anomaly of nasal bone
  • Congenital anomaly of palatine bone
  • Congenital anomaly of parietal bone
  • Congenital anomaly of premaxilla
  • Congenital anomaly of presphenoid bone
  • Congenital anomaly of squamosal bone
  • Congenital anomaly of supraoccipital bone
  • Congenital anomaly of supraoccipital bone
  • Congenital anomaly of supraoccipital bone
  • Congenital anomaly of supraoccipital bone
  • Congenital anomaly of supraoccipital bone
  • Congenital anomaly of supraoccipital bone
  • Congenital anomaly of supraoccipital bone
  • Congenital anomaly of supraoccipital bone
  • Congenital anomaly of tympanic anulus
  • Congenital anomaly of vomer
  • Congenital anomaly of zygomatic bone
  • Congenital asymmetry of forehead
  • Congenital atresia of nares
  • Congenital atresia of nasopharynx
  • Congenital atresia of pharynx
  • Congenital deformity of forehead
  • Congenital dyserythropoietic anemia
  • Congenital enlargement of fontanel
  • Congenital facial asymmetry
  • Congenital fenestration of alisphenoid bone
  • Congenital fenestration of basioccipital bone
  • Congenital fenestration of basisphenoid bone
  • Congenital fenestration of exoccipital bone
  • Congenital fenestration of frontal bone
  • Congenital fenestration of interparietal bone
  • Congenital fenestration of nasal bone
  • Congenital fenestration of parietal bone
  • Congenital fenestration of premaxilla
  • Congenital fenestration of presphenoid bone
  • Congenital fenestration of squamosal bone
  • Congenital fenestration of supraoccipital bone
  • Congenital hypertrophy of sphenoid bone
  • Congenital hypoplasia of alisphenoid bone
  • Congenital hypoplasia of basioccipital bone
  • Congenital hypoplasia of basisphenoid bone
  • Congenital hypoplasia of cerebrum
  • Congenital hypoplasia of clavicle
  • Congenital hypoplasia of exoccipital bone
  • Congenital hypoplasia of frontal bone
  • Congenital hypoplasia of interparietal bone
  • Congenital hypoplasia of lacrimal bone
  • Congenital hypoplasia of nasal bone
  • Congenital hypoplasia of nasal septum
  • Congenital hypoplasia of nose
  • Congenital hypoplasia of parietal bone
  • Congenital hypoplasia of premaxilla
  • Congenital hypoplasia of presphenoid bone
  • Congenital hypoplasia of squamosal bone
  • Congenital hypoplasia of supraoccipital bone
  • Congenital hypoplasia of tympanic anulus
  • Congenital hypoplasia of vomer
  • Congenital hypoplasia of zygomatic bone
  • Congenital J shaped sella turcica
  • Congenital malformation of anterior pituitary
  • Congenital malformation of sphenoid wing
  • Craniofacial cleft
  • Craniofacial conodysplasia syndrome
  • Craniofacial dysplasia osteopenia syndrome
  • Craniofacial microsomia
  • Craniofaciofrontodigital syndrome
  • Craniolacunia
  • Craniolacunia
  • Craniolenticulosutural dysplasia
  • Cranioosteoarthropathy
  • Cranioschisis
  • Cytochrome-c oxidase deficiency
  • Defect of skull ossification
  • Delayed membranous cranial ossification
  • Disorder of lacrimal bone
  • Domed head
  • Doughnut lesion of calvaria and bone fragility syndrome
  • Endosteal hyperostoses
  • Enlarged parietal foramina
  • Exocrine pancreatic insufficiency
  • Facial asymmetry
  • Frontal bossing
  • Frontal dysostosis
  • Frontonasal dysplasia sequence
  • Frontonasal dysplasia sequence
  • Frontonasal dysplasia sequence
  • Frontonasal dysplasia, bifid nose, upper limb anomalies syndrome
  • Frontorhiny
  • Hyperostosis cranialis interna
  • Hypertelorism
  • Incomplete ossification of alisphenoid bone
  • Incomplete ossification of basioccipital bone
  • Incomplete ossification of basisphenoid bone
  • Incomplete ossification of exoccipital bone
  • Incomplete ossification of frontal bone
  • Incomplete ossification of interparietal bone
  • Incomplete ossification of nasal bone
  • Incomplete ossification of palatine bone
  • Incomplete ossification of parietal bone
  • Incomplete ossification of premaxilla
  • Incomplete ossification of presphenoid bone
  • Incomplete ossification of skull
  • Incomplete ossification of squamosal bone
  • Incomplete ossification of supraoccipital bone
  • Incomplete ossification of tympanic anulus
  • Incomplete ossification of zygomatic bone
  • Infraorbital facial cleft - Tessier cleft 4
  • Infraorbital facial cleft - Tessier cleft 5
  • Infraorbital facial cleft - Tessier cleft 6
  • Infraorbital facial cleft - Tessier cleft 7
  • Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome
  • Lack of ossification of alisphenoid bone
  • Lack of ossification of basioccipital bone
  • Lack of ossification of basisphenoid bone
  • Lack of ossification of exoccipital bone
  • Lack of ossification of frontal bone
  • Lack of ossification of interparietal bone
  • Lack of ossification of nasal bone
  • Lack of ossification of palatine bone
  • Lack of ossification of parietal bone
  • Lack of ossification of premaxilla
  • Lack of ossification of presphenoid bone
  • Lack of ossification of squamosal bone
  • Lack of ossification of supraoccipital bone
  • Lack of ossification of tympanic anulus
  • Lack of ossification of zygomatic bone
  • Leptocephaly
  • Localized congenital skull defect
  • Localized congenital skull defect
  • MacDermot Winter syndrome
  • Metopic ridging, ptosis, facial dysmorphism syndrome
  • Microbrachycephaly, ptosis, cleft lip syndrome
  • Midline facial cleft - Tessier cleft 0
  • Midline facial cleft - Tessier cleft 14
  • Midline facial cleft - Tessier cleft 30
  • Occipital dysplasia
  • Osteosclerosis
  • Overgrowth, macrocephaly, facial dysmorphism syndrome
  • Overriding skull bones
  • Pancreatic insufficiency
  • Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome
  • Paramedian facial cleft - Tessier cleft 1
  • Paramedian facial cleft - Tessier cleft 2
  • Paramedian facial cleft - Tessier cleft 3
  • Parietal foramina with clavicular hypoplasia
  • Platybasia
  • Posterior perimaxillary faciosynostosis
  • Robin sequence
  • Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome
  • Short stature, pituitary and cerebellar defect and small sella turcica syndrome
  • Short stature, wormian bones, dextrocardia syndrome
  • SIX2-related frontonasal dysplasia
  • Spheno-fronto-parietal craniofaciosynostosis
  • Supraorbital facial cleft - Tessier cleft 10
  • Supraorbital facial cleft - Tessier cleft 11
  • Supraorbital facial cleft - Tessier cleft 12
  • Supraorbital facial cleft - Tessier cleft 13
  • Supraorbital facial cleft - Tessier cleft 8
  • Supraorbital facial cleft - Tessier cleft 9
  • Vomero-premaxillary faciosynostosis
  • Wormian bone of cranium
  • X-linked intellectual disability, craniofacioskeletal syndrome

Diagnostic Related Group(s)

The code Q75.8 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
  • Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
  • Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

References to Index of Diseases and Injuries

The code Q75.8 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Absence of skull bone, congenital
    • Congenital deformity of forehead
    • Platybasia

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
Q75.8 Right Arrow 756.0 Anomal skull/face bones

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
Q75 Other congenital malformations of skull and face bones
Q75.0 Craniosynostosis
Q75.00 Craniosynostosis unspecified
Q75.001 Craniosynostosis unspecified, unilateral
Q75.002 Craniosynostosis unspecified, bilateral
Q75.009 Craniosynostosis unspecified
Q75.01 Sagittal craniosynostosis
Q75.02 Coronal craniosynostosis
Q75.021 Coronal craniosynostosis unilateral
Q75.022 Coronal craniosynostosis bilateral
Q75.029 Coronal craniosynostosis unspecified
Q75.03 Metopic craniosynostosis
Q75.04 Lambdoid craniosynostosis
Q75.041 Lambdoid craniosynostosis, unilateral
Q75.042 Lambdoid craniosynostosis, bilateral
Q75.049 Lambdoid craniosynostosis, unspecified
Q75.05 Multi-suture craniosynostosis
Q75.051 Cloverleaf skull
Q75.052 Pansynostosis
Q75.058 Other multi-suture craniosynostosis
Q75.08 Other single-suture craniosynostosis
Q75.1 Craniofacial dysostosis
Q75.2 Hypertelorism
Q75.3 Macrocephaly
Q75.4 Mandibulofacial dysostosis
Q75.5 Oculomandibular dysostosis
Q75.9 Congenital malformation of skull and face bones, unspecified


This page was last updated on: 10/1/2023