Q04.9
BillableCongenital malformation of brain, unspecified
Congenital malformation of brain, unspecified
Status
Billable / Specific
Parent Code
Q04Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Congenital anomaly NOS of brain
- Congenital deformity NOS of brain
- Congenital disease or lesion NOS of brain
- Multiple anomalies NOS of brain, congenital
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Bilateral paralysis6481005
- Diplegia6481005
- Familial visceral neuropathy20725005
- Choreoathetosis43105007
- Atresia of duodenum51118003
- Congenital atresia of duodenum51118003
- Duodenal atresia51118003
- Cerebro-costo-mandibular syndrome51780007
- Cerebrocostomandibular syndrome51780007
- Rib gap defects with micrognathia51780007
- Bruch-de Lange syndrome55016009
- Congenital muscular hypertrophy-cerebral syndrome55016009
- Congenital hypotrichia56558005
- Congenital hypotrichosis56558005
- Hypotrichosis congenita56558005
- Congenital anomaly of brain57148006
- Congenital brain anomaly57148006
- Congenital disease of brain57148006
- Deformity of brain57148006
- Spastic paralysis78403003
- Congenital brain damage95610008
- Anomalies of cerebellum204047001
- Multiple anomalies of brain204074000
- Multiple brain anomalies204074000
- Disorder of ornithine metabolism237928008
- Ornithine metabolism disorder237928008
- Cerebellar cortical dysplasia253179009
- Dysplasia with defective mineralisation254117007
- Dysplasia with defective mineralization254117007
- Bilateral renal hypoplasia268232000
- Combined malformation of central nervous system and skeletal muscle277949001
- Spastic diplegia281411007
- PHPV - persistent hyperplastic primary vitreous314270008
- Persistent fetal vasculature syndrome314270008
- Persistent foetal vasculature syndrome314270008
- Persistent hyperplastic primary vitreous314270008
- Aplasia cutis congenita secondary to malformation syndrome (Type 9)403553002
- Delleman-Oorthuys syndrome403554008
- Oculocerebrocutaneous syndrome403554008
- Congenital anomaly of cerebrum702628006
- CODAS (cerebro-oculo-dento-auriculo-skeletal) syndrome717772000
- CODAS syndrome717772000
- Cerebro-oculo-dento-auriculo-skeletal syndrome717772000
- Brain malformation, congenital heart disease, postaxial polydactyly syndrome717943008
- Goossens Devriendt syndrome717943008
- BRESEK (brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia) syndrome717945001
- BRESEK syndrome717945001
- Brain anomaly, severe intellectual disability, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome717945001
- Brain anomaly, severe mental retardation, ectodermal dysplasia, skeletal deformity, ear anomaly, kidney dysplasia syndrome717945001
- X-linked mental retardation Reish type717945001
- Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome719833004
- Bakrania Ragge syndrome721878003
- Microphthalmia with brain and digit anomaly721878003
- Syndromic microphthalmia type 6721878003
- Oculo-palato-cerebral dwarfism722055008
- Oculo-palato-cerebral syndrome722055008
- Oculopalatocerebral syndrome722055008
- ECO (endocrine-cerebro-osteodysplasia) syndrome723309006
- ECO syndrome723309006
- Endocrine cerebroosteodysplasia syndrome723309006
- Endocrine-cerebro-osteodysplasia syndrome723309006
- Congenital hypoplasia of left kidney762913001
- Hypoplasia of left kidney762913001
- Left renal hypoplasia762913001
- Congenital hypoplasia of right kidney762914007
- Hypoplasia of right kidney762914007
- Right renal hypoplasia762914007
- Autosomal recessive intellectual disability due to TRAPPC9 (trafficking protein particle complex 9) deficiency763350002
- Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome763350002
- Cerebrofacioarticular syndrome763353000
- Van Maldergem syndrome763353000
- COXPD12 - combined oxidative phosphorylation defect type 12763366000
- Combined oxidative phosphorylation defect type 12763366000
- Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome763366000
- Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome765089003
- Focal epilepsy, intellectual disability, dysarthria, ataxia syndrome765089003
- X-linked cerebral, cerebellar, coloboma syndrome770604006
- X-linked intellectual disability Kroes type770604006
- Franek Bocker Kahlen syndrome770655004
- Microcephalus, brain defect, spasticity, hypernatraemia syndrome770655004
- Microcephalus, brain defect, spasticity, hypernatremia syndrome770655004
- Hypernatraemia771115008
- Hypernatremia771115008
- Na excess771115008
- Na overload771115008
- Sodium overload771115008
- Mitochondrial DNA depletion syndrome hepatocerebrorenal form782771007
- Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form782771007
- Muscle eye brain disease with bilateral multicystic leucodystrophy785298001
- Muscle eye brain disease with bilateral multicystic leukodystrophy785298001
- Microphthalmos due to Delleman syndrome1003369001
- Congenital corneal dystrophy1003408005
- Congenital dystrophy of cornea1003408005
- Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome1169355000
- ZTTK syndrome1169355000
- Zhu Tokita Takenouchi Kim syndrome1169355000
- Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome1172594000
- Congenital disorder of glycosylation due to PIGG (phosphatidylinositol glycan anchor biosynthesis class G) deficiency1172627007
- Congenital disorder of glycosylation due to phosphatidylinositol glycan anchor biosynthesis class G deficiency1172627007
- Early-onset epilepsy, intellectual disability, brain anomalies syndrome1172627007
- PIGG-CDG - congenital disorder of glycosylation due to PIGG deficiency1172627007
- Hunter Jurenka Thompson syndrome1208341008
- ORC (oculo-renal-cerebellar) syndrome1208341008
- Oculorenocerebellar syndrome1208341008
- Severe oculo-renal-cerebellar syndrome1208341008
- Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies1208985003
- RHOA (ras homolog family member A) related mosaic ectodermal dysplasia1208985003
- RHOA-related mosaic ectodermal dysplasia1208985003
- Bachmann Bupp syndrome1222658006
- Global developmental delay, alopecia, macrocephaly, facial dysmorphism, structural brain anomalies syndrome1222658006
- Ornithine decarboxylase deficiency1222658006
- Lethal brain and heart developmental defects syndrome1229876001
- Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome1237470001
- Oculo-cerebro-dental syndrome1255268002
- Oculocerebrodental syndrome1255268002
- Epilepsy due to congenital anomaly of brain1260377005
- Epilepsy with congenital anomaly of brain1260377005
- Progressive chorea27751000119104
UMLS
- Brain MalformationsC0266449
- Brain malformationC0266449
- Brain malformationsC0266449
- Congenital anomaly NOS of brainC0266449
- Congenital anomaly of brainC0266449
- Congenital anomaly of brain (disorder)C0266449
- Congenital brain anomalyC0266449
- Congenital brain anomaly NOSC0266449
- Congenital deformity NOS of brainC0266449
- Congenital malformation of brain, unspecifiedC0266449
- Deformity of brainC0266449
- brain deformitiesC0266449
- brain deformityC0266449
- brain malformationC0266449
- brain malformationsC0266449
- malformation brainC0266449
- Congenital disease or lesion NOS of brainC2910101
- Multiple anomalies NOS of brain, congenitalC2910102
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.
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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.