PRUNE1-related neurological syndrome 1222657001
SNOMED CT code
| SNOMED code | 1222657001 |
|---|---|
| name | PRUNE1-related neurological syndrome |
| status | active |
| date introduced | 2022-05-31 |
| fully specified name(s) | Prune exopolyphosphatase 1-related neurological syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Central nervous system structure 21483005 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group4 | |
| Interprets | Intellectual ability 247573007 |
| 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 PRUNE1-related neurological syndrome 1222657001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental delay 248290002 Global developmental delay 224958001 PRUNE1-related neurological syndrome 1222657001 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 PRUNE1-related neurological syndrome 1222657001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 PRUNE1-related neurological syndrome 1222657001 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 PRUNE1-related neurological syndrome 1222657001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 PRUNE1-related neurological syndrome 1222657001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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