Diagnosis Code

Q75.009 CRANIOSYNOSTOSIS UNSPECIFIED


Code Information

Diagnosis Code: Q75.009

Short Description: Craniosynostosis unspecified

Long Description: Craniosynostosis unspecified

The code Q75.009 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)
        • Q75.009 Craniosynostosis unspecified

Code Version: 2022 ICD-10-CM


Synonyms

  • Acrocephalosyndactyly type V
  • Acrocephalosyndactyly type V
  • Acrocephalosyndactyly type V
  • Acrocephaly
  • Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome
  • Agenesis of fibula
  • Ambiguous genitalia
  • Baller-Gerold syndrome
  • Closure of fontanelle
  • Complex craniosynostosis
  • Congenital agammaglobulinemia
  • Craniomicromelic syndrome
  • Craniorhiny
  • Craniosynostosis and dental anomalies syndrome
  • Craniosynostosis and intracranial calcification syndrome
  • Craniosynostosis Boston type
  • Craniosynostosis fibular aplasia syndrome
  • Craniosynostosis Herrmann Opitz type
  • Craniosynostosis Philadelphia type
  • Craniosynostosis syndrome
  • Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome
  • Craniosynostosis, anal anomaly, porokeratosis syndrome
  • Dandy-Walker syndrome
  • Early fontanel closure
  • Fibroblast growth factor receptor 3-related craniosynostosis
  • Frontonasal dysplasia sequence
  • Holoprosencephaly craniosynostosis syndrome
  • Hunter McAlpine craniosynostosis syndrome
  • Imperfect fusion of skull
  • Marfanoid physique
  • Muenke syndrome
  • Osteocraniostenosis
  • Osteosclerosis, developmental delay, craniosynostosis syndrome
  • Pfeiffer syndrome type 1
  • Pfeiffer syndrome type 2
  • Pfeiffer syndrome type 3
  • SCARF syndrome
  • Shprintzen Goldberg craniosynostosis syndrome
  • Simple craniosynostosis
  • Spondyloepiphyseal dysplasia, craniosynostosis, cleft palate, cataract and intellectual disability syndrome

Diagnostic Related Group(s)

The code Q75.009 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 Q75.009 has the following ICD-10-CM references to the Index of Diseases and Injuries
  • Inclusion Terms:
    • Imperfect fusion of skull

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
Q75.01 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
Q75.8 Other specified congenital malformations of skull and face bones
Q75.9 Congenital malformation of skull and face bones, unspecified


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