Cross syndrome 17827007
SNOMED CT code
SNOMED code | 17827007 |
---|---|
name | Cross syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Cross syndrome (disorder) |
synonyms |
|
attributes - group3 | |
Pathological process | Pathological developmental process 308490002 |
Finding site | Skin structure 39937001 |
Associated morphology | Decreased melanin pigmentation 37257004 |
Occurrence | Congenital 255399007 |
attributes - group4 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Decreased melanin pigmentation 37257004 |
Finding site | Eye structure 81745001 |
Occurrence | Congenital 255399007 |
attributes - group1 | |
Interprets | Adaptation behavior 406208005 |
Has interpretation | Impaired 260379002 |
attributes - group2 | |
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 Cross syndrome 17827007 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Oculocutaneous albinism 63844009 Cross syndrome 17827007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Cross syndrome 17827007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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