SNOMED CT, US Edition

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/SNOMEDCT/698848005
http://purl.bioontology.org/ontology/SNOMEDCT/698848005
Preferred Name

Hereditary retinal dystrophy primarily involving sensory retina
Synonyms
Inherited retinal dystrophy primarily involving sensory retina
Hereditary retinal dystrophy primarily involving sensory retina (disorder)
Type http://www.w3.org/2002/07/owl#Class

All Properties

prefLabel
Hereditary retinal dystrophy primarily involving sensory retina
altLabel
Inherited retinal dystrophy primarily involving sensory retina
Hereditary retinal dystrophy primarily involving sensory retina (disorder)
Type ID
900000000000003001
900000000000013009
Semantic type UMLS property
Has finding site
Effective time
20140131
cui
C3697292
CTV3ID
XUmUK
DEFINITION STATUS ID
900000000000074008
CASE SIGNIFICANCE ID
900000000000448009
tui
T047
Active
1
Has associated morphology
notation
698848005
type
subClassOf
Subset member
447562003~MAPRULE~TRUE
900000000000497000~MAPTARGET~XUmUK
6011000124106~MAPADVICE~ALWAYS H35.53
6011000124106~MAPGROUP~1
447562003~MAPADVICE~ALWAYS H35.5
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPTARGET~H35.53
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
447562003~MAPTARGET~H35.5
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
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