Keutel syndrome 724208006
SNOMED CT code
SNOMED code | 724208006 |
---|---|
name | Keutel syndrome |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Keutel syndrome (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Pulmonary artery within lung 128260003 |
Associated morphology | Stenosis 415582006 |
attributes - group4 | |
Occurrence | Congenital 255399007 |
Associated morphology | Pathologic calcification 18115005 |
Finding site | Cartilage structure 771314001 |
Pathological process | Pathological developmental process 308490002 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Face structure 89545001 |
attributes - group3 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Abnormally short growth 11182007 |
Finding site | Digit structure 82680008 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Finding of limb structure 302293008 Disorder of limb 128605003 Congenital anomaly of limb 60475009 Multiple malformation syndrome with facial-limb defects as major feature 23359005 Keutel syndrome 724208006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Calcinosis 6595006 Chondrocalcinosis 239838005 Keutel syndrome 724208006 SNOMED CT Concept 138875005 Clinical finding 404684003 Respiratory finding 106048009 Lower respiratory tract finding 301226008 Congenital anomaly of lower respiratory system 123654008 Congenital anomaly of lung 47147007 Congenital peripheral pulmonary artery stenosis 286071000119109 Keutel syndrome 724208006 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Keutel syndrome 724208006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Connective tissue hereditary disorder 363045008 Keutel syndrome 724208006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Keutel syndrome 724208006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Keutel syndrome 724208006 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of limb structure 302293008 Deformity of limb 445144002 Longitudinal deficiency of part of limb 716638009 Brachydactyly 43476002 Keutel syndrome 724208006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of connective tissue 105969002 Congenital connective tissue disorder 363039000 Congenital anomaly of cartilage 67988000 Keutel syndrome 724208006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Keutel syndrome 724208006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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