SNOMED CT

Last uploaded: January 31, 2024

Preferred Name	Congenital retinal fold
Synonyms	Congenital retinal fold (disorder)
ID	http://purl.bioontology.org/ontology/SNOMEDCT/204181009
Active	1
altLabel	Congenital retinal fold (disorder)
CASE SIGNIFICANCE ID	900000000000448009
CTV3ID	P3551
cui	C0344550
DEFINITION STATUS ID	900000000000074008
Effective time	20020131
Has associated morphology	http://purl.bioontology.org/ontology/SNOMEDCT/49755003
Has finding site	http://purl.bioontology.org/ontology/SNOMEDCT/5665001
Has pathological process	http://purl.bioontology.org/ontology/SNOMEDCT/308490002
notation	204181009
Occurs in	http://purl.bioontology.org/ontology/SNOMEDCT/255399007
prefLabel	Congenital retinal fold
Subset member	447562003~MAPADVICE~ALWAYS Q14.8 447562003~MAPRULE~TRUE 447562003~MAPTARGET~Q14.8 6011000124106~MAPGROUP~1 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPADVICE~ALWAYS Q14.1 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 6011000124106~MAPTARGET~Q14.1 6011000124106~MAPRULE~TRUE 900000000000497000~MAPTARGET~P3551
tui	T019
Type ID	900000000000003001 900000000000013009
subClassOf	http://purl.bioontology.org/ontology/SNOMEDCT/49381001

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/SCTSPA/204181009	SCTSPA	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU005717	OMIM	CUI
http://purl.bioontology.org/ontology/RCTV2/P355100	RCTV2	LOOM