Pettigrew syndrome 719139003
SNOMED CT code
| SNOMED code | 719139003 |
|---|---|
| name | Pettigrew syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Face structure 89545001 |
| attributes - group4 | |
| Finding site | Cerebellar vermis structure 58501004 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Hypoplasia 55199003 |
| attributes - group6 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Cystic dilatation 125269003 |
| Finding site | Fourth ventricle structure 35918002 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Basal ganglion structure 32610002 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Cerebellar vermis structure 58501004 |
| Associated morphology | Congenital malrotation 48641006 |
| attributes - group5 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Cystic dilatation 125269003 |
| Finding site | Infratentorial brain structure 21031007 |
| attributes - group7 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group8 | |
| 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 Pettigrew syndrome 719139003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 Pettigrew syndrome 719139003 SNOMED CT Concept 138875005 Clinical finding 404684003 Neurological lesion 299735001 Lesion of brain 301766008 Cystic malformation of posterior fossa 35111000119109 Dandy-Walker syndrome 14447001 Pettigrew syndrome 719139003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Pettigrew syndrome 719139003 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 Pettigrew syndrome 719139003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Pettigrew syndrome 719139003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Disorder of basal ganglia 70835005 Pettigrew syndrome 719139003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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