SNOMED CT

Last uploaded: August 27, 2019
Preferred Name

Autosomal dominant hereditary disorder

Synonyms

Autosomal dominant hereditary disorder (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/11164009

Active

1

altLabel

Autosomal dominant hereditary disorder (disorder)

AD - Autosomal dominant

CASE SIGNIFICANCE ID

900000000000017005

900000000000448009

900000000000020002

CTV3ID

XU2ur

cui

C0265385

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

notation

11164009

prefLabel

Autosomal dominant hereditary disorder

Subset member

6011000124106~MAPPRIORITY~1

900000000000509007~ACCEPTABILITYID~900000000000548007

447562003~MAPGROUP~1

6011000124106~MAPTARGET~Q99.9

447562003~MAPCATEGORYID~447637006

6011000124106~MAPCATEGORYID~447637006

6011000124106~MAPRULE~TRUE

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPGROUP~1

6011000124106~CORRELATIONID~447561005

900000000000509007~ACCEPTABILITYID~900000000000549004

447562003~MAPADVICE~ALWAYS Q99.9

447562003~MAPTARGET~Q99.9

447562003~MAPRULE~TRUE

447562003~MAPPRIORITY~1

900000000000497000~MAPTARGET~XU2ur

447562003~CORRELATIONID~447561005

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPADVICE~ALWAYS Q99.9 | DESCENDANTS NOT EXHAUSTIVELY MAPPED

tui

T047

Type ID

900000000000013009

900000000000003001

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/1899006

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/SCTSPA/11164009 SCTSPA CUI
http://purl.bioontology.org/ontology/SNMI/D4-02002 SNMI CUI
http://www.owl-ontologies.com/Ontology1358660052.owl#Autosomal_Dominant_Hereditary_Disorder PEDTERM LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/11164009 NLMVS SAME_URI