Diagnosis Code: Q75.9

Short Description: Congenital malformation of skull and face bones, unspecified

Long Description: Congenital malformation of skull and face bones, unspecified

The code Q75.9 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)
      • Q75.9 Congenital malformation of skull and face bones, unspecified

Code Version: 2022 ICD-10-CM

Synonyms

• Athetoid cerebral palsy
• Autosomal dominant intellectual disability, craniofacial anomalies, cardiac defects syndrome
• Brachycephaly
• Cardiocranial syndrome Pfeiffer type
• Cleft lip and palate, craniofacial dysmorphism, congenital heart defect, hearing loss syndrome
• Congenital abnormality of skull and face bones
• Congenital anomaly of alisphenoid bone
• Congenital anomaly of basisphenoid bone
• Congenital anomaly of face bones
• Congenital anomaly of fetal head bones
• Congenital anomaly of head
• Congenital anomaly of skull
• Congenital anomaly of supraoccipital bone
• Congenital diaphragmatic hernia
• Congenital dilatation of colon
• Congenital malformation of sphenoid wing
• Congenital posterolateral diaphragmatic hernia
• Craniofacial deafness hand syndrome
• Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome
• Deafness craniofacial syndrome
• Diaphragmatic defect, limb deficiency, skull defect syndrome
• Dyskinetic cerebral palsy
• Haspeslagh Fryns Muelenaere syndrome
• Hemifacial microsomia
• Hirschsprung disease with nail hypoplasia and dysmorphism
• Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome
• Localized congenital skull defect
• Mitochondrial DNA depletion syndrome encephalomyopathic form
• Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
• Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome
• Non-spastic cerebral palsy
• Oculo-auriculo-vertebral spectrum
• Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome
• Skull congenital deformities

Diagnostic Related Group(s)

The code Q75.9 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 Q75.9 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital anomaly of face bones NOS
  • Congenital anomaly of skull NOS

Crosswalk Information

Similar Codes

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

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