SNOMED CT

Last uploaded: August 27, 2019
Preferred Name

Congenital pigmentary skin anomalies

Synonyms

Congenital pigmentary anomaly of skin

ID

http://purl.bioontology.org/ontology/SNOMEDCT/205564003

Active

1

altLabel

Congenital pigmentary anomaly of skin

Congenital pigmentary skin anomalies (disorder)

CASE SIGNIFICANCE ID

900000000000448009

CTV3ID

PH32.

cui

C0009726

DEFINITION STATUS ID

900000000000073002

Effective time

20150731

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/21390004

http://purl.bioontology.org/ontology/SNOMEDCT/79644001

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/39937001

notation

205564003

Occurs in

http://purl.bioontology.org/ontology/SNOMEDCT/255399007

prefLabel

Congenital pigmentary skin anomalies

Subset member

6011000124106~MAPPRIORITY~1

6011000124106~MAPADVICE~ALWAYS Q82.1 | DESCENDANTS NOT EXHAUSTIVELY MAPPED

900000000000509007~ACCEPTABILITYID~900000000000548007

447562003~MAPGROUP~1

447562003~MAPCATEGORYID~447637006

900000000000497000~MAPTARGET~PH32.

6011000124106~MAPCATEGORYID~447637006

6011000124106~MAPRULE~TRUE

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPGROUP~1

447562003~MAPADVICE~ALWAYS Q82.8

6011000124106~CORRELATIONID~447561005

900000000000509007~ACCEPTABILITYID~900000000000549004

447562003~MAPRULE~TRUE

447562003~MAPPRIORITY~1

447562003~CORRELATIONID~447561005

447562003~MAPTARGET~Q82.8

6011000124106~MAPTARGET~Q82.1

900000000000508004~ACCEPTABILITYID~900000000000549004

tui

T019

Type ID

900000000000013009

900000000000003001

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/46690002

http://purl.bioontology.org/ontology/SNOMEDCT/199879009

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MEDDRA/10010593 MEDDRA CUI
http://purl.bioontology.org/ontology/ICD9CM/757.33 ICD9CM CUI
http://purl.bioontology.org/ontology/RCTV2/PH32.00 RCTV2 LOOM
http://purl.bioontology.org/ontology/SNMI/D4-40350 SNMI CUI