Brain malformation
CODAS (cerebro-oculo-dento-auriculo-skeletal) syndrome
Brain malformations
Syndromic microphthalmia type 6
Microcephalus, brain defect, spasticity, hypernatraemia syndrome
Bachmann Bupp syndrome
Autosomal recessive intellectual disability due to TRAPPC9 (trafficking protein particle complex 9) deficiency
Endocrine cerebroosteodysplasia syndrome
Congenital brain anomaly
Diplegia
Oculo-palato-cerebral syndrome
Congenital deformity NOS of brain
COXPD12 - combined oxidative phosphorylation defect type 12
Congenital disease of brain
Hunter Jurenka Thompson syndrome
Hypoplasia of left kidney
Disorder of ornithine metabolism
Delleman-Oorthuys syndrome
Van Maldergem syndrome
Oculorenocerebellar syndrome
Cerebro-oculo-dento-auriculo-skeletal syndrome
ZTTK syndrome
Duodenal atresia
Cerebrocostomandibular syndrome
Congenital muscular hypertrophy-cerebral syndrome
ECO syndrome
Multiple anomalies of brain
Epilepsy with congenital anomaly of brain
Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome
Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome
Focal epilepsy, intellectual disability, dysarthria, ataxia syndrome
Congenital hypotrichosis
Dysplasia with defective mineralization
Multiple brain anomalies
X-linked intellectual disability Kroes type
Oculo-palato-cerebral dwarfism
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome
Congenital anomaly of brain (disorder)
Hypotrichosis congenita
PIGG-CDG - congenital disorder of glycosylation due to PIGG deficiency
Bilateral renal hypoplasia
Hypoplasia of right kidney
Lethal brain and heart developmental defects syndrome
Microcephalus, brain defect, spasticity, hypernatremia syndrome
Bakrania Ragge syndrome
Muscle eye brain disease with bilateral multicystic leucodystrophy
Dysplasia with defective mineralisation
Na excess
Na overload
Progressive chorea
Cerebellar cortical dysplasia
Early-onset epilepsy, intellectual disability, brain anomalies syndrome
PHPV - persistent hyperplastic primary vitreous
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome
Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome
BRESEK (brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia) syndrome
Oculocerebrocutaneous syndrome
Epilepsy due to congenital anomaly of brain
Spastic paralysis
Hypernatremia
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome
Muscle eye brain disease with bilateral multicystic leukodystrophy
Cerebrofacioarticular syndrome
Zhu Tokita Takenouchi Kim syndrome
Congenital corneal dystrophy
Congenital disorder of glycosylation due to PIGG (phosphatidylinositol glycan anchor biosynthesis class G) deficiency
Left renal hypoplasia
Oculo-cerebro-dental syndrome
Ornithine metabolism disorder
X-linked cerebral, cerebellar, coloboma syndrome
brain deformity
Congenital hypotrichia
Severe oculo-renal-cerebellar syndrome
Bruch-de Lange syndrome
CODAS syndrome
Anomalies of cerebellum
Oculopalatocerebral syndrome
Combined malformation of central nervous system and skeletal muscle
Congenital anomaly NOS of brain
ECO (endocrine-cerebro-osteodysplasia) syndrome
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies
Deformity of brain
RHOA (ras homolog family member A) related mosaic ectodermal dysplasia
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome
Combined oxidative phosphorylation defect type 12
Spastic diplegia
Congenital disease or lesion NOS of brain
Goossens Devriendt syndrome
Multiple anomalies NOS of brain, congenital
RHOA-related mosaic ectodermal dysplasia
Congenital anomaly of brain
Congenital disorder of glycosylation due to phosphatidylinositol glycan anchor biosynthesis class G deficiency
Microphthalmos due to Delleman syndrome
Congenital hypoplasia of right kidney
brain deformities
Congenital brain damage
X-linked mental retardation Reish type
Bilateral paralysis
BRESEK syndrome
Microphthalmia with brain and digit anomaly
Cerebro-costo-mandibular syndrome
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome
Rib gap defects with micrognathia
Familial visceral neuropathy
Mitochondrial DNA depletion syndrome hepatocerebrorenal form
Aplasia cutis congenita secondary to malformation syndrome (Type 9)
Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome
Oculocerebrodental syndrome
Atresia of duodenum
Choreoathetosis
Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form
Persistent hyperplastic primary vitreous
Right renal hypoplasia
Congenital atresia of duodenum
malformation brain
Ornithine decarboxylase deficiency
Persistent foetal vasculature syndrome
Brain malformation, congenital heart disease, postaxial polydactyly syndrome
Congenital anomaly of cerebrum
Persistent fetal vasculature syndrome
Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome
Congenital dystrophy of cornea
Sodium overload
Hypernatraemia
Endocrine-cerebro-osteodysplasia syndrome
ORC (oculo-renal-cerebellar) syndrome
Congenital brain anomaly NOS
Franek Bocker Kahlen syndrome
Congenital hypoplasia of left kidney

Frequently Asked Questions

What is the ICD-10 code for congenital malformation of brain, unspecified?

The ICD-10-CM code for congenital malformation of brain, unspecified is Q04.9. The full clinical description is "Congenital malformation of brain, unspecified". Q04.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q04.9 mean?

ICD-10-CM code Q04.9 represents “Congenital malformation of brain, unspecified”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q04.9 a billable code?

Yes, Q04.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q04.9 in?

Q04.9 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q04.9?

Q04.9 has Excludes1 notes indicating codes that cannot be used together with it, including: cyclopia (Q87.0); macrocephaly (Q75.3).

What SNOMED CT codes does Q04.9 map to?

Q04.9 maps to 53 SNOMED CT concepts: 204047001, 403553002, 51118003, 763350002, 717945001, and 48 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q04.9?

Q04.9 is linked to 3 UMLS Concept Unique Identifiers: C0266449, C2910101, C2910102. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q04.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation of brain, unspecified affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q04.9?

Q04.9 maps to the ICD-11 code: LA05.Z (Cerebral structural developmental anomalies, unspecified).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.