Microcephaly, thin corpus callosum, intellectual disability syndrome 770721009
SNOMED CT code
| SNOMED code | 770721009 |
|---|---|
| name | Microcephaly, thin corpus callosum, intellectual disability syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Microcephaly, thin corpus callosum, intellectual disability syndrome (disorder) |
| synonyms | Microcephaly, thin corpus callosum, intellectual disability syndrome |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | Corpus callosum structure 88442005 |
| attributes - group2 | |
| Interprets | Head circumference 363812007 |
| Has interpretation | Below reference range 281300000 |
| attributes - group3 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group4 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 Microcephaly, thin corpus callosum, intellectual disability syndrome 770721009 SNOMED CT Concept 138875005 Clinical finding 404684003 Body measurement finding 365605003 Finding of head circumference 301338002 Microcephaly 1148757008 Microcephaly, thin corpus callosum, intellectual disability syndrome 770721009 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Leukoencephalopathy 22811006 Congenital malformation of corpus callosum 204042007 Microcephaly, thin corpus callosum, intellectual disability syndrome 770721009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Microcephaly, thin corpus callosum, intellectual disability syndrome 770721009 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, thin corpus callosum, intellectual disability syndrome 770721009 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, thin corpus callosum, intellectual disability syndrome 770721009 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, thin corpus callosum, intellectual disability syndrome 770721009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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