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ICD-10-CM Codes
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Q00-Q99
Congenital malformations, deformations and chromosomal abnormalities
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Q65-Q79
Congenital malformations and deformations of the musculoskeletal system
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Q75-
Other congenital malformations of skull and face bones
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2021 ICD-10-CM Diagnosis Code Q75.1
2021 ICD-10-CM Diagnosis Code Q75.1
Craniofacial dysostosis
2016 2017 2018 2019 2020 2021 Billable/Specific Code POA Exempt
- Q75.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2021 edition of ICD-10-CM Q75.1 became effective on October 1, 2020.
- This is the American ICD-10-CM version of Q75.1 - other international versions of ICD-10 Q75.1 may differ.
The following code(s) above
Q75.1 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
Q75.1:
- A syndrome inherited in an autosomal dominant pattern. It is characterized by early fusion of the bones of the skull and face. Patients have a distinctive facial appearance which includes low-set ears, brachycephaly, hypertelorism, exophthalmos, and mandibular prognathism.
- Autosomal dominant craniosynostosis with shallow orbits; exophthalmos; and maxillary hypoplasia.
- Autosomal dominant disorder characterized by acrocephaly, exophthalmos, hypertelorism, strabismus, parrot-beaked nose, and hypoplastic maxilla with relative mandibular prognathism.
Present On AdmissionPOA Help
"Present On Admission" is defined as present at the time the order for inpatient admission occurs — conditions that develop during an outpatient encounter, including emergency department, observation, or outpatient surgery, are considered POA.
- Q75.1 is considered exempt from POA reporting.
ICD-10-CM Q75.1 is grouped within Diagnostic Related Group(s) (MS-DRG v38.0):
- 564 Other musculoskeletal system and connective tissue diagnoses with mcc
- 565 Other musculoskeletal system and connective tissue diagnoses with cc
- 566 Other musculoskeletal system and connective tissue diagnoses without cc/mcc
Convert Q75.1 to ICD-9-CM
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
ICD-10-CM Codes Adjacent To Q75.1
Q73.8 Other reduction defects of unspecified limb(s)
Q74 Other congenital malformations of limb(s)
Q74.0 Other congenital malformations of upper limb(s), including shoulder girdle
Q74.1 Congenital malformation of knee
Q74.2 Other congenital malformations of lower limb(s), including pelvic girdle
Q74.3 Arthrogryposis multiplex congenita
Q74.8 Other specified congenital malformations of limb(s)
Q74.9 Unspecified congenital malformation of limb(s)
Q75 Other congenital malformations of skull and face bones
Q75.1
Craniofacial dysostosis
Q75.4 Mandibulofacial dysostosis
Q75.5 Oculomandibular dysostosis
Q75.8 Other specified congenital malformations of skull and face bones
Q75.9 Congenital malformation of skull and face bones, unspecified
Q76 Congenital malformations of spine and bony thorax
Q76.0 Spina bifida occulta
Q76.1 Klippel-Feil syndrome
Q76.2 Congenital spondylolisthesis
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
