Lelis syndrome 719429003
SNOMED CT code
SNOMED code | 719429003 |
---|---|
name | Lelis syndrome |
status | active |
date introduced | 2017-01-31 |
fully specified name(s) | Ectodermal dysplasia with acanthosis nigricans syndrome (disorder) |
synonyms |
|
attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Finding site | Skin structure 39937001 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
attributes - group3 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dysplasia 25723000 |
Occurrence | Congenital 255399007 |
Finding site | Ectoderm structure 63206006 |
attributes - group1 | |
Has interpretation | Abnormal 263654008 |
Interprets | Keratinization 44138005 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Disorder of keratinization 277905003 Inherited disorder of keratinization 254214009 Lelis syndrome 719429003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Lelis syndrome 719429003 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Disorder of keratinization 277905003 Acanthosis nigricans 402599005 Lelis syndrome 719429003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Lelis syndrome 719429003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Lelis syndrome 719429003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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