X-linked neurodegenerative syndrome Hamel type 718847005
SNOMED CT code
| SNOMED code | 718847005 |
|---|---|
| name | X-linked neurodegenerative syndrome Hamel type |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | X-linked neurodegenerative syndrome Hamel type (disorder) |
| synonyms | X-linked neurodegenerative syndrome Hamel type |
| attributes - group1 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Nervous system structure 25087005 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| 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 X-linked neurodegenerative syndrome Hamel type 718847005 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 X-linked neurodegenerative syndrome Hamel type 718847005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 X-linked neurodegenerative syndrome Hamel type 718847005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 X-linked neurodegenerative syndrome Hamel type 718847005 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 X-linked neurodegenerative syndrome Hamel type 718847005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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