Microcephaly, polymicrogyria, corpus callosum agenesis syndrome 773305003
SNOMED CT code
| SNOMED code | 773305003 |
|---|---|
| name | Microcephaly, polymicrogyria, corpus callosum agenesis syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) |
| synonyms | Microcephaly, polymicrogyria, corpus callosum agenesis syndrome |
| attributes - group1 | |
| Associated morphology | Congenital smallness 41086002 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Gyrus of brain 3964001 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Entire corpus callosum 362354006 |
| Associated morphology | Agenesis 782173000 |
| attributes - group3 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | Birth head circumference 169876006 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Body measurement finding 365605003 Finding of head circumference 301338002 Microcephaly 1148757008 Congenital microcephaly 1148758003 Microcephaly, polymicrogyria, corpus callosum agenesis syndrome 773305003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Microcephaly, polymicrogyria, corpus callosum agenesis syndrome 773305003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Microcephaly, polymicrogyria, corpus callosum agenesis syndrome 773305003 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Disorder of neuronal migration and differentiation 253146009 Microgyria 4945003 Microcephaly, polymicrogyria, corpus callosum agenesis syndrome 773305003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Hemianencephaly 85641006 Aplasia of corpus callosum 204044008 Agenesis of corpus callosum 5102002 Microcephaly, polymicrogyria, corpus callosum agenesis syndrome 773305003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Microcephaly, polymicrogyria, corpus callosum agenesis syndrome 773305003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Microcephaly, polymicrogyria, corpus callosum agenesis syndrome 773305003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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