Certain infectious and parasitic diseases
Certain infectious and parasitic diseases Certain infectious and parasitic diseases
Q01.0 Frontal encephalocele Q01.1 Nasofrontal encephalocele Q01.2 Occipital encephalocele Q01.8 Encephalocele of other sites Q01.9 Encephalocele, unspecified Q02 Q03 Microcephaly Hydromicrocephaly Micrencephalon Excludes: Meckel-Gruber syndrome ( Q61.9 ) Congenital hydrocephalus Includes: hydrocephalus in newborn Excludes: Arnold-Chiari syndrome ( Q07.0 ) hydrocephalus: · acquired ( G91.- ) · due to congenital toxoplasmosis ( P37.1 ) · with spina bifida ( Q05.0-Q05.4 ) Q03.0 Malformations of aqueduct of Sylvius Aqueduct of Sylvius: · anomaly · obstruction, congenital · stenosis Q03.1 Atresia of foramina of Magendie and Luschka Dandy-Walker syndrome Q03.8 Other congenital hydrocephalus Q03.9 Congenital hydrocephalus, unspecified Q04 Other congenital malformations of brain Excludes: cyclopia ( Q87.0 ) macrocephaly ( Q75.3 ) Q04.0 Congenital malformations of corpus callosum Agenesis of corpus callosum Q04.1 Arhinencephaly Q04.2 Holoprosencephaly Q04.3 Other reduction deformities of brain Absence Agenesis of part of brain Aplasia Hypoplasia 538 WHO’s ICD-10
Agyria Hydranencephaly Lissencephaly Microgyria Pachygyria Excludes: congenital malformations of corpus callosum ( Q04.0 ) Q04.4 Septo-optic dysplasia Q04.5 Megalencephaly Q04.6 Congenital cerebral cysts Porencephaly Schizencephaly Excludes: acquired porencephalic cyst ( G93.0 ) Q04.8 Other specified congenital malformations of brain Macrogyria Q04.9 Congenital malformation of brain, unspecified Congenital: · anomaly · deformity · disease or lesion · multiple anomalies NOS of brain Q05 Spina bifida Includes: hydromeningocele (spinal) meningocele (spinal) meningomyelocele myelocele myelomeningocele rachischisis spina bifida (aperta)(cystica) syringomyelocele Excludes: Arnold-Chiari syndrome ( Q07.0 ) spina bifida occulta ( Q76.0 ) Q05.0 Cervical spina bifida with hydrocephalus Q05.1 Thoracic spina bifida with hydrocephalus Spina bifida: · dorsal · thoracolumbar } with hydrocephalus Q05.2 Lumbar spina bifida with hydrocephalus Lumbosacral spina bifida with hydrocephalus Q05.3 Sacral spina bifida with hydrocephalus Q05.4 Unspecified spina bifida with hydrocephalus Version for 2007 539
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Q01.0 Frontal encephalocele<br />
Q01.1 Nasofrontal encephalocele<br />
Q01.2 Occipital encephalocele<br />
Q01.8 Encephalocele of other sites<br />
Q01.9 Encephalocele, unspecified<br />
Q02<br />
Q03<br />
Microcephaly<br />
Hydromicrocephaly<br />
Micrencephalon<br />
Excludes: Meckel-Gruber syndrome ( Q61.9 )<br />
Congenital hydrocephalus<br />
Includes: hydrocephalus in newborn<br />
Excludes: Arnold-Chiari syndrome ( Q07.0 )<br />
hydrocephalus:<br />
· acquired ( G91.- )<br />
· due to congenital toxoplasmosis ( P37.1 )<br />
· with spina bifida ( Q05.0-Q05.4 )<br />
Q03.0 Malformations of aqueduct of Sylvius<br />
Aqueduct of Sylvius:<br />
· anomaly<br />
· obstruction, congenital<br />
· stenosis<br />
Q03.1 Atresia of foramina of Magendie <strong>and</strong> Luschka<br />
D<strong>and</strong>y-Walker syndrome<br />
Q03.8 Other congenital hydrocephalus<br />
Q03.9 Congenital hydrocephalus, unspecified<br />
Q04 Other congenital malformations of brain<br />
Excludes: cyclopia ( Q87.0 )<br />
macrocephaly ( Q75.3 )<br />
Q04.0 Congenital malformations of corpus callosum<br />
Agenesis of corpus callosum<br />
Q04.1 Arhinencephaly<br />
Q04.2 Holoprosencephaly<br />
Q04.3 Other reduction deformities of brain<br />
Absence<br />
Agenesis<br />
of part of brain<br />
Aplasia<br />
Hypoplasia<br />
538 WHO’s ICD-10
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