https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:ICD-11_Neural_anomalies_table&feed=atom&action=history
Template:ICD-11 Neural anomalies table - Revision history
2024-03-28T22:39:46Z
Revision history for this page on the wiki
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https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:ICD-11_Neural_anomalies_table&diff=375683&oldid=prev
Z8600021 at 22:45, 1 April 2019
2019-04-01T22:45:23Z
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Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:ICD-11_Neural_anomalies_table&diff=375669&oldid=prev
Z8600021 at 22:38, 1 April 2019
2019-04-01T22:38:15Z
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| </div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}1292761836 LA00.0 Anencephaly] - {{ICD11weblink}}1558931335 LA00.1 Iniencephaly], {{ICD11weblink}}546224466 LA00.2 Acephaly]<del style="font-weight: bold; text-decoration: none;">, </del>{{ICD11weblink}}154698183 LA00.3 Amyelencephaly]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}1292761836 LA00.0 Anencephaly] - <ins style="font-weight: bold; text-decoration: none;">a neural tube defect, characterized by the total or partial absence of the cranial vault and the covering skin, the brain being missing or reduced to a small mass. Most cases are stillborn, although some infants have been reported to survive for a few hours. In most cases autopsy findings reveal absence of adrenal glands. Anencephaly is likely to be multifactorial, the result of gene-environment interactions. Familial cases with a seemingly autosomal recessive mode of inheritance have been described but most cases are sporadic. Folic acid and zinc deficiencies, as well as maternal obesity, have been shown to be risk factors.</ins></div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}1520916568 LA01 Cephalocele]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>{{ICD11weblink}}1558931335 LA00.1 Iniencephaly] <ins style="font-weight: bold; text-decoration: none;">- a rare form of neural tube defect in which a malformation of the cervico-occipital junction is associated with a malformation of the central nervous system. The cardinal features are occipital bone defect</ins>, <ins style="font-weight: bold; text-decoration: none;">partial or total absence of cervicothoracic vertebrae, fetal retroflexion of the head and characteristic absence of the neck. It is associated with malformations of the central nervous (spina bifida and/or anencephaly), gastrointestinal (omphalocele) and cardiovascular systems.</ins></div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}2036217905 LA02 Spina bifida] - LA02.0 Spina bifida cystica<del style="font-weight: bold; text-decoration: none;">, </del>LA02.00 Myelomeningocele with hydrocephalus, LA02.01 Myelomeningocele without hydrocephalus, LA02.02 Myelocystocele, LA02.1 Spina bifida aperta <del style="font-weight: bold; text-decoration: none;"> </del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>{{ICD11weblink}}546224466 LA00.2 Acephaly]</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}1987349422 LA03 Arnold-Chiari malformation type II]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">* </ins>{{ICD11weblink}}154698183 LA00.3 Amyelencephaly] <ins style="font-weight: bold; text-decoration: none;">- Amyelencephaly is the absence of both the brain and spinal cord.</ins></div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}1878746673 LA04 Congenital hydrocephalus]</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}1520916568 LA01 Cephalocele] <ins style="font-weight: bold; text-decoration: none;">- failure of the skull to correctly close during the antenatal period. This condition is characterized by herniation of the meninges. This condition may present with herniation of brain, or developmental delay. Confirmation is through observation of herniated meninges by imaging.</ins></div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}327560976 LA05 Cerebral structural developmental anomalies] <del style="font-weight: bold; text-decoration: none;">- </del>LA05.0 Microcephaly<del style="font-weight: bold; text-decoration: none;">, </del>LA05.1 Megalencephaly<del style="font-weight: bold; text-decoration: none;">, </del>LA05.2 Holoprosencephaly<del style="font-weight: bold; text-decoration: none;">, </del>LA05.3 Corpus callosum agenesis<del style="font-weight: bold; text-decoration: none;">, </del>LA05.4 Arhinencephaly<del style="font-weight: bold; text-decoration: none;">, </del>LA05.5 Abnormal neuronal migration<del style="font-weight: bold; text-decoration: none;">, </del>LA05.6 Encephaloclastic disorders<del style="font-weight: bold; text-decoration: none;">, </del>LA05.7 Brain cystic malformations </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}2036217905 LA02 Spina bifida] - </div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}1642909021 LA06 Cerebellar structural developmental anomalies] <del style="font-weight: bold; text-decoration: none;">- </del>LA06.0 Dandy-Walker malformation<del style="font-weight: bold; text-decoration: none;">, </del>LA06.1 Hypoplasia or agenesis of cerebellar hemispheres<del style="font-weight: bold; text-decoration: none;">, </del>LA06.2 Focal cerebellar dysplasia </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** {{ICD11weblink}}979482551 </ins>LA02.0 Spina bifida cystica<ins style="font-weight: bold; text-decoration: none;">] - failure of the neural tube to correctly develop during the antenatal period. This condition is characterized by nerve damage and the presence of meningoceles on the back. This condition may present with physical or mental impairment.</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** {{ICD11weblink}}182894151 </ins>LA02.00 Myelomeningocele with hydrocephalus<ins style="font-weight: bold; text-decoration: none;">] - failure of the neural tube to correctly develop during the antenatal period. This condition is characterized by nerve damage and hydrocephalus. This condition may also present with syringomyelia, hip dislocation, headache, nausea, vomiting, blurry vision, balance problems, bladder control problems, meningitis</ins>, <ins style="font-weight: bold; text-decoration: none;">or mental impairment.</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** {{ICD11weblink}}1008004337 </ins>LA02.01 Myelomeningocele without hydrocephalus<ins style="font-weight: bold; text-decoration: none;">] - failure of the neural tube to close completely during fetal development. This condition is characterized by nerve damage. This condition may also present with syringomyelia, hip dislocation, headache, nausea, vomiting, blurry vision, balance problems</ins>, <ins style="font-weight: bold; text-decoration: none;">bladder control problems, meningitis, or mental impairment.</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** {{ICD11weblink}}863949070 </ins>LA02.02 Myelocystocele<ins style="font-weight: bold; text-decoration: none;">] - failure of the neural tube to close completely during fetal development. The condition is characterized by skin covered lumbosacral masses, an arachnoid lined meningocele that is directly continuous with the spinal subarachnoid space</ins>, <ins style="font-weight: bold; text-decoration: none;">and a low lying hydromyelic spinal cord that traverses the meningocele and expands into a large terminal cyst. This condition can present with neural damage and consequent impairment of function below the site of the myelocystocele.</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** {{ICD11weblink}}187581000 </ins>LA02.1 Spina bifida aperta<ins style="font-weight: bold; text-decoration: none;">] - failure of the neural tube to correctly develop during the antenatal period. This condition is characterized by nerve damage originating from a known location in the spine, signified by the presence of a meningocele or myelomeningocele. This condition may present with physical or mental impairment.</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}1987349422 LA03 Arnold-Chiari malformation type II] <ins style="font-weight: bold; text-decoration: none;">- failure of the brain and spinal cord to correctly develop during the antenatal period. This condition is characterized by extension of both cerebellar and brain stem tissue into the foramen magnum. This condition may present with partial or complete absence of the cerebellar vermis, myelomeningocele, neck pain, balance problems, muscle weakness, limb numbness, dizziness, vision problems, difficulty swallowing, ringing in the ears, hearing loss, vomiting, insomnia, depression, or impairment of motor skills.</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}1878746673 LA04 Congenital hydrocephalus] <ins style="font-weight: bold; text-decoration: none;">- failure of the brain to correctly develop during the antenatal period. This condition is characterized by a rapid increase in head circumference or an unusually large head size due to excessive accumulation of cerebrospinal fluid in the brain. This condition may also present with vomiting, sleepiness, irritability, downward deviation of the eyes, or seizures. Confirmation is through observation of cerebrospinal fluid within cerebral ventricles by imaging.</ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}327560976 LA05 Cerebral structural developmental anomalies]</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA05.0 Microcephaly</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA05.1 Megalencephaly</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA05.2 Holoprosencephaly</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA05.3 Corpus callosum agenesis</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA05.4 Arhinencephaly</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA05.5 Abnormal neuronal migration</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA05.6 Encephaloclastic disorders</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA05.7 Brain cystic malformations </div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}1642909021 LA06 Cerebellar structural developmental anomalies]</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA06.0 Dandy-Walker malformation</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA06.1 Hypoplasia or agenesis of cerebellar hemispheres</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">** </ins>LA06.2 Focal cerebellar dysplasia </div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}725439990 LA07 Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>* {{ICD11weblink}}725439990 LA07 Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column]</div></td></tr>
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Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:ICD-11_Neural_anomalies_table&diff=375657&oldid=prev
Z8600021 at 22:32, 1 April 2019
2019-04-01T22:32:45Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 09:32, 2 April 2019</td>
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Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:ICD-11_Neural_anomalies_table&diff=375649&oldid=prev
Z8600021: Created page with "{| |-bgcolor="FFCC00" ! {{ICD-11}} {{ICD11weblink}}215057274 '''LA00-LA0Z''' Structural developmental anomalies of the nervous system] |-bgcolor="FEF9E7" | * {{ICD11weblink}}..."
2019-04-01T22:30:25Z
<p>Created page with "{| |-bgcolor="FFCC00" ! {{ICD-11}} {{ICD11weblink}}215057274 '''LA00-LA0Z''' Structural developmental anomalies of the nervous system] |-bgcolor="FEF9E7" | * {{ICD11weblink}}..."</p>
<p><b>New page</b></p><div>{|<br />
|-bgcolor="FFCC00"<br />
! {{ICD-11}} {{ICD11weblink}}215057274 '''LA00-LA0Z''' Structural developmental anomalies of the nervous system]<br />
|-bgcolor="FEF9E7"<br />
| <br />
* {{ICD11weblink}}1292761836 LA00.0 Anencephaly] - {{ICD11weblink}}1558931335 LA00.1 Iniencephaly], {{ICD11weblink}}546224466 LA00.2 Acephaly], {{ICD11weblink}}154698183 LA00.3 Amyelencephaly]<br />
* {{ICD11weblink}}1520916568 LA01 Cephalocele]<br />
* {{ICD11weblink}}2036217905 LA02 Spina bifida] - LA02.0 Spina bifida cystica, LA02.00 Myelomeningocele with hydrocephalus, LA02.01 Myelomeningocele without hydrocephalus, LA02.02 Myelocystocele, LA02.1 Spina bifida aperta <br />
* {{ICD11weblink}}1987349422 LA03 Arnold-Chiari malformation type II]<br />
* {{ICD11weblink}}1878746673 LA04 Congenital hydrocephalus]<br />
* {{ICD11weblink}}327560976 LA05 Cerebral structural developmental anomalies] - LA05.0 Microcephaly, LA05.1 Megalencephaly, LA05.2 Holoprosencephaly, LA05.3 Corpus callosum agenesis, LA05.4 Arhinencephaly, LA05.5 Abnormal neuronal migration, LA05.6 Encephaloclastic disorders, LA05.7 Brain cystic malformations <br />
* {{ICD11weblink}}1642909021 LA06 Cerebellar structural developmental anomalies] - LA06.0 Dandy-Walker malformation, LA06.1 Hypoplasia or agenesis of cerebellar hemispheres, LA06.2 Focal cerebellar dysplasia <br />
* {{ICD11weblink}}725439990 LA07 Structural developmental anomalies of the neurenteric canal, spinal cord or vertebral column]<br />
|}</div>
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