SNOMED CT

Last uploaded: August 28, 2024
Preferred Name

Hereditary disease
Synonyms

Inherited disease

Hereditary disease (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/32895009

Active

1

altLabel

Inherited disease

Hereditary disease (disorder)

Associated finding of

http://purl.bioontology.org/ontology/SNOMEDCT/700102000

http://purl.bioontology.org/ontology/SNOMEDCT/429962007

http://purl.bioontology.org/ontology/SNOMEDCT/81651000119109

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

Cause of

http://purl.bioontology.org/ontology/SNOMEDCT/402808004

http://purl.bioontology.org/ontology/SNOMEDCT/733203002

http://purl.bioontology.org/ontology/SNOMEDCT/1260396009

http://purl.bioontology.org/ontology/SNOMEDCT/707183006

CTV3ID

XUBrO

cui

C0019247

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

Focus of

http://purl.bioontology.org/ontology/SNOMEDCT/79841006

http://purl.bioontology.org/ontology/SNOMEDCT/702598006

http://purl.bioontology.org/ontology/SNOMEDCT/702597001

INACTIVATION INDICATOR

723278000

notation

32895009

Occurs before

http://purl.bioontology.org/ontology/SNOMEDCT/363299008

prefLabel

Hereditary disease

Realization of

http://purl.bioontology.org/ontology/SNOMEDCT/721131000124101

Subset member

6011000124106~MAPTARGET~Z14.8

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~ALWAYS Z14.8 | DESCENDANTS NOT EXHAUSTIVELY MAPPED

900000000000531004~TARGETCOMPONENT~782964007

900000000000497000~MAPTARGET~XUBrO

6011000124106~MAPGROUP~1

447562003~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPTARGET~

447562003~MAPPRIORITY~1

6011000124106~MAPPRIORITY~1

900000000000490003~VALUEID~723278000

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~TRUE

900000000000509007~ACCEPTABILITYID~900000000000549004

447562003~MAPCATEGORYID~447638001

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/782964007

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/LNC/LP62869-0 LOINC CUI
http://purl.bioontology.org/ontology/LNC/MTHU021573 LOINC CUI
http://purl.bioontology.org/ontology/MDRGER/10061205 MDRGER CUI
http://purl.bioontology.org/ontology/MEDDRA/10019873 MEDDRA CUI
http://purl.bioontology.org/ontology/SCTSPA/782964007 SCTSPA CUI
http://purl.bioontology.org/ontology/LNC/LP56740-1 LOINC CUI
http://purl.bioontology.org/ontology/PDQ/CDR0000256156 PDQ CUI
http://purl.bioontology.org/ontology/MDRFRE/10019873 MDRFRE CUI
http://purl.bioontology.org/ontology/RCD/Xa4hE RCD CUI
http://purl.bioontology.org/ontology/MDRGER/10019873 MDRGER CUI
http://purl.bioontology.org/ontology/SCTSPA/32895009 SCTSPA CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0019247 MEDLINEPLUS CUI
http://purl.bioontology.org/ontology/MDRFRE/10061205 MDRFRE CUI
http://purl.bioontology.org/ontology/MEDDRA/10061205 MEDDRA CUI
http://purl.bioontology.org/ontology/MESH/D030342 MESH CUI
http://purl.bioontology.org/ontology/CSP/1254-7727 CRISP CUI
http://purl.bioontology.org/ontology/LNC/MTHU025721 LOINC CUI
http://purl.bioontology.org/ontology/MSHFRE/D030342 MSHFRE CUI
http://purl.bioontology.org/ontology/SNMI/DF-00180 SNMI CUI
http://purl.obolibrary.org/obo/DOID_630 CLO LOOM
http://purl.jp/bio/4/id/200906003143939281 IOBC LOOM
http://purl.obolibrary.org/obo/MONDO_0003847 GCBO LOOM
http://purl.obolibrary.org/obo/MONDO_0003847 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0003847 DOVES LOOM
http://purl.obolibrary.org/obo/MONDO_0003847 GENEPIO LOOM
http://purl.obolibrary.org/obo/MONDO_0003847 OBA LOOM