Congenital pontocerebellar hypoplasia type 10 782720005
SNOMED CT code
SNOMED code | 782720005 |
---|---|
name | Congenital pontocerebellar hypoplasia type 10 |
status | active |
date introduced | 2019-07-31 |
fully specified name(s) | Congenital pontocerebellar hypoplasia type 10 (disorder) |
synonyms |
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attributes - group1 | |
Associated morphology | Hypoplasia 55199003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Cerebellar structure 113305005 |
attributes - group2 | |
Associated morphology | Hypoplasia 55199003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Pontine structure 49557009 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Congenital pontocerebellar hypoplasia type 10 782720005 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 Congenital pontocerebellar hypoplasia type 10 782720005 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 Dysgenesis of the brainstem 253180007 Congenital pontocerebellar hypoplasia 45163000 Congenital pontocerebellar hypoplasia type 10 782720005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Congenital pontocerebellar hypoplasia type 10 782720005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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