SNOMED CT

Last uploaded: August 28, 2024
Preferred Name

Hereditary retinal dystrophy
Synonyms

Hereditary retinal dystrophy (disorder)

ID

http://purl.bioontology.org/ontology/SNOMEDCT/41799005

Active

1

altLabel

Hereditary retinal dystrophy (disorder)

CASE SIGNIFICANCE ID

900000000000020002

900000000000448009

CTV3ID

F427.

cui

C0154860

DEFINITION STATUS ID

900000000000074008

Effective time

20020131

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/4720007

Has finding site

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

notation

41799005

prefLabel

Hereditary retinal dystrophy

Subset member

447562003~MAPRULE~TRUE

6011000124106~MAPGROUP~1

447562003~MAPADVICE~ALWAYS H35.5

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

6011000124106~MAPADVICE~ALWAYS H35.50 | DESCENDANTS NOT EXHAUSTIVELY MAPPED

900000000000509007~ACCEPTABILITYID~900000000000548007

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPTARGET~H35.50

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

447562003~MAPTARGET~H35.5

6011000124106~MAPPRIORITY~1

6011000124106~CORRELATIONID~447561005

900000000000497000~MAPTARGET~F427.

6011000124106~MAPRULE~TRUE

900000000000509007~ACCEPTABILITYID~900000000000549004

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

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

http://purl.bioontology.org/ontology/SNOMEDCT/314407005

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/RCD/F427. RCD CUI
http://purl.bioontology.org/ontology/SCTSPA/41799005 SCTSPA CUI
http://purl.bioontology.org/ontology/MDRGER/10019899 MDRGER CUI
http://purl.bioontology.org/ontology/ICD9CM/362.7 ICD9CM CUI
http://purl.bioontology.org/ontology/MDRFRE/10019899 MDRFRE CUI
http://purl.bioontology.org/ontology/MDRGER/10019898 MDRGER CUI
http://purl.bioontology.org/ontology/MEDDRA/10019900 MEDDRA CUI
http://purl.bioontology.org/ontology/MEDDRA/10019899 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRFRE/10019900 MDRFRE CUI
http://purl.bioontology.org/ontology/MEDDRA/10019898 MEDDRA CUI
http://purl.bioontology.org/ontology/ICD10CM/H35.5 ICD10CM CUI
http://purl.bioontology.org/ontology/ICD10CM/H35.50 ICD10CM CUI
http://purl.bioontology.org/ontology/SNMI/DA-71900 SNMI CUI
http://purl.bioontology.org/ontology/ICD9CM/362.70 ICD9CM CUI
http://purl.bioontology.org/ontology/ICD10/H35.5 ICD10 CUI
http://purl.bioontology.org/ontology/MDRFRE/10019898 MDRFRE CUI
http://purl.bioontology.org/ontology/MDRGER/10019900 MDRGER CUI
http://purl.bioontology.org/ontology/SNOMEDCT/41799005 NLMVS SAME_URI
http://purl.bioontology.org/ontology/RCD/F427. RCD LOOM
http://purl.obolibrary.org/obo/DOID_8500 CLO LOOM
http://purl.obolibrary.org/obo/DOID_8500 DOID LOOM
http://purl.obolibrary.org/obo/DOID_8500 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_8500 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_8500 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_8500 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_8500 FNS-H LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Hereditary_Retinal_Dystrophy CSEO LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_8500 NATPRO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C35194 NCIT LOOM
http://purl.bioontology.org/ontology/MEDDRA/10019899 MEDDRA LOOM
http://purl.bioontology.org/ontology/ICD10CM/H35.5 ICD10CM LOOM
http://purl.bioontology.org/ontology/ICD10/H35.5 ICD10 LOOM
http://purl.obolibrary.org/obo/NCIT_C35194 BERO LOOM