CHILD syndrome 17608003
SNOMED CT code
SNOMED code | 17608003 |
---|---|
name | CHILD syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome (disorder) |
synonyms |
|
attributes - group1 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Skin structure 39937001 |
Occurrence | Congenital 255399007 |
attributes - group3 | |
Interprets | Keratinization 44138005 |
Has interpretation | Abnormal 263654008 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Finding site | Limb structure 66019005 |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
parents |
|
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked dominant hereditary disease 1162984000 CHILD syndrome 17608003 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 CHILD syndrome 17608003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital ichthyosiform erythroderma 254156001 CHILD syndrome 17608003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of lipoprotein AND/OR lipid metabolism 48286001 Disorder of lipid metabolism 267431006 CHILD syndrome 17608003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 CHILD syndrome 17608003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Multiple malformation syndrome with limb defect as major feature 41443008 CHILD syndrome 17608003 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Congenital anomaly of limb 60475009 CHILD syndrome 17608003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 CHILD syndrome 17608003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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