Diagnosis Code: Q04.9

Short Description: Congenital malformation of brain, unspecified

Long Description: Congenital malformation of brain, unspecified

The code Q04.9 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Congenital malformations of the nervous system (Q00-Q07)
    • Other congenital malformations of brain (Q04)
      • Q04.9 Congenital malformation of brain, unspecified

Code Version: 2022 ICD-10-CM

Synonyms

• Anomalies of cerebellum
• Aplasia cutis congenita secondary to malformation syndrome
• Bilateral renal hypoplasia
• Brain malformation, congenital heart disease, postaxial polydactyly syndrome
• Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome
• BRESEK syndrome
• Cerebellar cortical dysplasia
• Cerebro-costo-mandibular syndrome
• Cerebrofacioarticular syndrome
• Choreoathetosis
• CODAS syndrome
• Combined malformation of central nervous system and skeletal muscle
• Congenital anomaly of brain
• Congenital anomaly of cerebrum
• Congenital atresia of duodenum
• Congenital brain damage
• Congenital corneal dystrophy
• Congenital hypotrichia
• Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome
• Congenital muscular hypertrophy-cerebral syndrome
• Diplegia
• Disorder of ornithine metabolism
• Dysplasia with defective mineralization
• Early-onset epilepsy, intellectual disability, brain anomalies syndrome
• Endocrine-cerebro-osteodysplasia syndrome
• Epilepsy due to congenital anomaly of brain
• Familial visceral neuropathy
• Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome
• Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome
• Hypernatremia
• Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome
• Left renal hypoplasia
• Lethal brain and heart developmental defects syndrome
• Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome
• Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome
• Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
• Microcephalus, brain defect, spasticity, hypernatremia syndrome
• Microphthalmia with brain and digit anomaly
• Microphthalmos due to Delleman syndrome
• Mitochondrial DNA depletion syndrome hepatocerebrorenal form
• Multiple brain anomalies
• Muscle eye brain disease with bilateral multicystic leukodystrophy
• Oculocerebrocutaneous syndrome
• Oculocerebrodental syndrome
• Oculopalatocerebral syndrome
• Persistent hyperplastic primary vitreous
• Right renal hypoplasia
• Severe oculo-renal-cerebellar syndrome
• Spastic diplegia
• Spastic paralysis
• Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome
• X-linked cerebral, cerebellar, coloboma syndrome

References to Index of Diseases and Injuries

The code Q04.9 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital anomaly NOS of brain
  • Congenital deformity NOS of brain
  • Congenital disease or lesion NOS of brain
  • Multiple anomalies NOS of brain, congenital

Crosswalk Information

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

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