Porencephaly, cerebellar hypoplasia, internal malformations syndrome 763821001
SNOMED CT code
SNOMED code | 763821001 |
---|---|
name | Porencephaly, cerebellar hypoplasia, internal malformations syndrome |
status | active |
date introduced | 2018-07-31 |
fully specified name(s) | Porencephaly, cerebellar hypoplasia, internal malformations syndrome (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Cystic dilatation 125269003 |
Occurrence | Congenital 255399007 |
Finding site | Brain structure 12738006 |
attributes - group3 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Hypoplasia 55199003 |
Finding site | Cerebellar structure 113305005 |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Associated morphology | Absence 418560003 |
Finding site | Cerebellar vermis structure 58501004 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Cerebellar disorder 223176004 Dysgenesis of the cerebellum 253171007 Congenital cerebellar hypoplasia 16026008 Porencephaly, cerebellar hypoplasia, internal malformations syndrome 763821001 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Cerebellar disorder 223176004 Absence of the vermis 253177006 Porencephaly, cerebellar hypoplasia, internal malformations syndrome 763821001 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 Congenital anomaly of brain 57148006 Anencephalus 89369001 Congenital absence of part of brain 26595007 Porencephaly, cerebellar hypoplasia, internal malformations syndrome 763821001 SNOMED CT Concept 138875005 Clinical finding 404684003 Neurological lesion 299735001 Lesion of brain 301766008 Congenital porencephaly 38353004 Porencephaly, cerebellar hypoplasia, internal malformations syndrome 763821001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Porencephaly, cerebellar hypoplasia, internal malformations syndrome 763821001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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