SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Hereditary factor II deficiency disease

Synonyms

Hereditary factor II deficiency disease (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/33297000

Active

1

altLabel

Hereditary factor II deficiency disease (disorder)

Hereditary hypoprothrombinemia

Hereditary hypoprothrombinaemia

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

CTV3ID

XUBwM

cui

C0272317

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

Has interpretation

http://purl.bioontology.org/ontology/SNOMEDCT/263654008

interprets

http://purl.bioontology.org/ontology/SNOMEDCT/74848003

notation

33297000

prefLabel

Hereditary factor II deficiency disease

Subset member

447562003~MAPRULE~TRUE

6011000124106~MAPTARGET~D68.2

6011000124106~MAPGROUP~1

447562003~MAPADVICE~ALWAYS D68.2 | MAPPED FOLLOWING WHO GUIDANCE

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

447562003~MAPTARGET~D68.2

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPADVICE~ALWAYS D68.2

6011000124106~MAPPRIORITY~1

900000000000497000~MAPTARGET~XUBwM

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~TRUE

900000000000509007~ACCEPTABILITYID~900000000000549004

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/73975000

http://purl.bioontology.org/ontology/SNOMEDCT/16922007

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