SNOMED CT

Last uploaded: August 28, 2024
Preferred Name

Atrophia bulborum hereditaria
Synonyms

Norrie's disease

Oligophrenia microphthalmus

Atrophia bulborum hereditaria (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/15228007

Active

1

altLabel

Norrie's disease

Oligophrenia microphthalmus

Atrophia bulborum hereditaria (disorder)

CASE SIGNIFICANCE ID

900000000000448009

900000000000017005

CTV3ID

X00dN

cui

C0266526

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/13331008

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/5665001

notation

15228007

prefLabel

Atrophia bulborum hereditaria

Subset member

447562003~MAPRULE~TRUE

447562003~MAPADVICE~ALWAYS Q99.8

6011000124106~MAPGROUP~1

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

447562003~CORRELATIONID~447561005

447562003~MAPTARGET~Q99.8

447562003~MAPTARGET~Q15.8

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPTARGET~Q15.8

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

900000000000497000~MAPTARGET~X00dN

6011000124106~MAPADVICE~ALWAYS Q15.8

6011000124106~MAPPRIORITY~1

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~TRUE

900000000000509007~ACCEPTABILITYID~900000000000549004

447562003~MAPADVICE~ALWAYS Q15.8

tui

T019

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/363343008

http://purl.bioontology.org/ontology/SNOMEDCT/405722004

http://purl.bioontology.org/ontology/SNOMEDCT/1162976004

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