Congenital iodine deficiency syndrome 217710005
SNOMED CT code
SNOMED code | 217710005 |
---|---|
name | Congenital iodine deficiency syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Congenital iodine deficiency syndrome (disorder) |
synonyms |
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attributes - group1 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Finding site | Thyroid structure 69748006 |
Occurrence | Congenital 255399007 |
parents | |
children | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of neck 118939000 Disorder of thyroid gland 14304000 Iodine deficiency syndrome 237562002 Congenital iodine deficiency syndrome 217710005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of neck 118939000 Disorder of thyroid gland 14304000 Congenital anomaly of the thyroid gland 32454003 Congenital iodine deficiency syndrome 217710005 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 due to non-infectious environmental agents 57544002 Congenital iodine deficiency syndrome 217710005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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