X-linked intellectual disability Van Esch type 718914002
SNOMED CT code
SNOMED code | 718914002 |
---|---|
name | X-linked intellectual disability Van Esch type |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | X-linked intellectual disability Van Esch type (disorder) |
synonyms | X-linked intellectual disability Van Esch type |
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Gonadal endocrine structure 304041004 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Mental disorder 74732009 Developmental mental disorder 129104009 Intellectual disability 110359009 X-linked intellectual disability Van Esch type 718914002 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 intellectual disability Van Esch type 718914002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hereditary disorder of endocrine system 363104002 X-linked intellectual disability Van Esch type 718914002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary disorder by system 363137000 Reproductive system hereditary disorder 363290007 X-linked intellectual disability Van Esch type 718914002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding by site 118234003 Disorder by body site 123946008 Disorder of body system 362965005 Disorder of endocrine system 362969004 Disorder of endocrine gonad 127345001 Hypogonadism 48130008 Primary hypogonadism 370999003 X-linked intellectual disability Van Esch type 718914002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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