Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) | | Microcephaly, polymicrogyria, corpus callosum agenesis syndrome | | A rare genetic central nervous system malformation syndrome with characteristics of marked prenatal-onset microcephaly, severe motor delay with hypotonia, bilateral polymicrogyria, corpus callosum agenesis, ventricular dilation, small cerebellum and early lethality. | | syndroom van microcefalie, polymicrogyrie en agenesie van corpus callosum |
| Id | 773305003 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | Q04.3 | Rule | TRUE | Advice | ALWAYS Q04.3 | Correlation | SNOMED CT source code to target map code correlation not specified |
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