ICD-10 Lookup - Find Medical Diagnosis Codes
ICD-10 Search Results for other-congenital-malformations-of-brain-q04
| ICD-10-CM Code | Description | Category | Valid for Submission |
|---|---|---|---|
| Q04 | Other congenital malformations of brain | Not Valid | |
| Q04.3 | Other reduction deformities of brain Congenital cerebellar hypoplasia; Congenital diaphragmatic hernia; Congenital chorioretinal degeneration; Congenital malformation of the meninges; Congenital malformation of anterior pituitary; Congenital absence of part of brain; Congenital agenesis of brainstem nuclei; Congenital conduction defect; Congenital porencephaly; Congenital hypoplasia of inner granular layer of cerebellum; Congenital bilateral perisylvian syndrome; Congenital pontocerebellar hypoplasia; Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration; Congenital pontocerebellar hypoplasia type 2; Congenital pontocerebellar hypoplasia type 7; Congenital pontocerebellar hypoplasia type 6; Congenital pontocerebellar hypoplasia type 5; Congenital pontocerebellar hypoplasia type 4; Congenital pontocerebellar hypoplasia type 3; Congenital pontocerebellar hypoplasia type 1; Congenital pontocerebellar hypoplasia type 8; Joubert syndrome with congenital hepatic fibrosis; Congenital pontocerebellar hypoplasia type 9; Congenital pontocerebellar hypoplasia type 10; Congenital muscular dystrophy with cerebellar involvement; Congenital hypoplasia of part of brain; Congenital hepatic fibrosis; Congenital hypoplasia of cerebrum; Congenital hypoplasia of cerebrum; Porencephaly, cerebellar hypoplasia, internal malformations syndrome; Agenesis of right hemisphere of cerebellum; Agenesis of left hemisphere of cerebellum; Dyke-Davidoff-Masson syndrome; Isolated agenesis of cerebellar vermis; Agenesis of cerebrum; Anomalies of hypothalamus; Aplasia of cerebellum; Abnormality of neurogenesis; Abnormality of neurogenesis; Abnormality of neurogenesis; Partial agenesis of corpus callosum; Absence of septum pellucidum; Dysgenesis of the cerebellum; Agenesis of cerebellum; Agenesis of cerebellum; Agenesis of cerebellum; Aplasia of the vermis; Familial aplasia of the vermis; Familial aplasia of the vermis; Familial aplasia of the vermis; Familial aplasia of the vermis; Familial aplasia of the vermis; Familial aplasia of the vermis; Familial aplasia of the vermis; Dysgenesis of the brainstem; Congenital malformation of the meninges; Hypoplasia of brain gyri; Congenital malformation of anterior pituitary; Congenital absence of part of brain; Combined malformation of central nervous system and skeletal muscle; Combined malformation of central nervous system and skeletal muscle; Congenital agenesis of brainstem nuclei; Congenital hypoplasia of inner granular layer of cerebellum; Partial absence of septum pellucidum; Joubert syndrome with orofaciodigital defect; Congenital hypoplasia of part of brain; Complete agenesis of vermis; Congenital hypoplasia of cerebrum; Congenital hypoplasia of cerebrum; Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome; Dysgenesis of the brainstem; Hypoplasia of brain gyri; Congenital absence of part of brain; Congenital agenesis of brainstem nuclei; Congenital hypoplasia of part of brain; | Valid | |
| Q04.8 | Other specified congenital malformations of brain Congenital cerebral ventriculomegaly; Congenital cerebral ventriculomegaly; Congenital pseudobulbar palsy; Congenital malformation of the meninges; Congenital sequelae of disorders; Congenital aniridia; Congenital intrauterine infection-like syndrome; Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi; Congenital abnormal shape of cerebellum; Congenital abnormal shape of cerebrum; Coffin-Siris syndrome; Hamartoma of hypothalamus; Abnormality of neurogenesis; Abnormality of neurogenesis; Defect of telencephalic division; Congenital malformation of the meninges; Hamartoma of brain; Cystic malformation of posterior fossa; Congenital sequelae of disorders; Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi; Congenital abnormal shape of cerebellum; Congenital abnormal shape of cerebrum; Hamartoma of brain; Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome; Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome; Athabaskan brainstem dysgenesis syndrome; | Valid |