Erythroderma in infancy (disorder)
SCTID: 733206005, Defined, Active
733206005 |Erythroderma in infancy (disorder)|
3498989010 - Erythroderma in infancy (en) View
3498990018 - Erythroderma in infancy (disorder) (en) View
Relationship (7079074022) - 733206005 -> 3658006 (246454002) View
Relationship (7079075023) - 733206005 -> 39937001 (363698007) View
Relationship (11355036022) - 733206005 -> 703938007 (116680003) View
Relationship (12092447024) - 733206005 -> 409774005 (116676008) View
Relationship (13274027027) - 733206005 -> 3658006 (246454002) View
Relationship (12498274028) - 733206005 -> 239091003 (116680003) View
Relationship (7079073027) - 733206005 -> 23583003 (116676008) View
Relationship (11381491022) - 733206005 -> 363169009 (116680003) View
Relationship (7079076024) - 733206005 -> 103626005 (116676008) View
Relationship (7079077026) - 733206005 -> 39937001 (363698007) View
Relationship (11355034020) - 733206005 -> 70819003 (116676008) View
Relationship (11355035021) - 733206005 -> 39937001 (363698007) View
Relationship (7079072021) - 733206005 -> 399992009 (116680003) View
399992009 View
239091003 View
240302002 View
ExtendedMap object (ff9157f5-f017-51a9-8390-b46bfa0cd948) View
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