SNOMED CT

Last uploaded: August 28, 2024

Preferred Name	Congenital atrophy of thyroid
Synonyms	Congenital atrophy of thyroid (disorder)
ID	http://purl.bioontology.org/ontology/SNOMEDCT/237517001
Active	1
altLabel	Congenital atrophy of thyroid (disorder)
CASE SIGNIFICANCE ID	900000000000448009
CTV3ID	X40HB
cui	C0342154
DEFINITION STATUS ID	900000000000073002
Effective time	20140731
Has associated morphology	http://purl.bioontology.org/ontology/SNOMEDCT/13331008
Has finding site	http://purl.bioontology.org/ontology/SNOMEDCT/69748006
notation	237517001
Occurs in	http://purl.bioontology.org/ontology/SNOMEDCT/255399007
prefLabel	Congenital atrophy of thyroid
Subset member	447562003~MAPRULE~TRUE 6011000124106~MAPADVICE~ALWAYS E03.1 6011000124106~MAPGROUP~1 900000000000497000~MAPTARGET~X40HB 447562003~MAPTARGET~E03.1 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPADVICE~ALWAYS E03.1 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPTARGET~E03.1 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 6011000124106~MAPRULE~TRUE
tui	T019
Type ID	900000000000003001 900000000000013009
subClassOf	http://purl.bioontology.org/ontology/SNOMEDCT/66091009 http://purl.bioontology.org/ontology/SNOMEDCT/190309006

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/SCTSPA/237517001	SCTSPA	CUI
http://purl.bioontology.org/ontology/ICD10CM/E03.1	ICD10CM	CUI
http://purl.bioontology.org/ontology/RCD/X40HB	RCD	CUI
http://purl.bioontology.org/ontology/RCD/X40HB	RCD	LOOM