SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Congenital hemihypertrophy

Synonyms

Congenital hemihypertrophy (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/205838004

Active

1

altLabel

Congenital hemihypertrophy (disorder)

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

CTV3ID

PKyz6

cui

C0332890

DEFINITION STATUS ID

900000000000074008

Effective time

20190131

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/56246009

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/423857001

Has pathological process

http://purl.bioontology.org/ontology/SNOMEDCT/308490002

INACTIVATION INDICATOR

900000000000482003

900000000000495008

notation

205838004

Occurs in

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

prefLabel

Congenital hemihypertrophy

Subset member

447562003~MAPRULE~TRUE

6011000124106~MAPGROUP~1

900000000000527005~TARGETCOMPONENT~56007004

900000000000490003~VALUEID~900000000000495008

447562003~MAPGROUP~1

900000000000489007~VALUEID~900000000000482003

447562003~CORRELATIONID~447561005

6011000124106~MAPTARGET~Q89.8

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

900000000000508004~ACCEPTABILITYID~900000000000548007

900000000000497000~MAPTARGET~PKyz6

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

447562003~MAPADVICE~ALWAYS Q87.3

6011000124106~MAPPRIORITY~1

6011000124106~MAPADVICE~ALWAYS Q89.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE

447562003~MAPTARGET~Q87.3

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~TRUE

tui

T019

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/276654001

Delete Subject Author Type Created
No notes to display