SNOMED CT

Last uploaded: August 28, 2024
Preferred Name

Hereditary nephritis
Synonyms

Hereditary nephritis (disorder)

Hereditary glomerulonephritis

GN - Hereditary glomerulonephritis

ID

http://purl.bioontology.org/ontology/SNOMEDCT/399340005

Active

1

altLabel

Hereditary nephritis (disorder)

Hereditary glomerulonephritis

GN - Hereditary glomerulonephritis

CASE SIGNIFICANCE ID

900000000000448009

900000000000017005

CTV3ID

XUYoI

cui

C0027706

DEFINITION STATUS ID

900000000000073002

Effective time

20030731

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/409777003

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/68288006

INACTIVATION INDICATOR

723278000

notation

399340005

prefLabel

Hereditary nephritis

Subset member

447562003~MAPRULE~TRUE

447562003~MAPADVICE~IF HEREDITARY DIFFUSE ENDOCAPILLARY PROLIFERATIVE GLOMERULONEPHRITIS CHOOSE N07.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION

447562003~MAPTARGET~N07.3

6011000124106~MAPTARGET~N07.9

447562003~MAPRULE~IFA 367531000119106 | Hereditary diffuse endocapillary proliferative glomerulonephritis (disorder) |

447562003~MAPADVICE~IF HEREDITARY DIFFUSE MESANGIOCAPILLARY GLOMERULONEPHRITIS CHOOSE N07.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION

6011000124106~MAPGROUP~1

447562003~MAPPRIORITY~6

447562003~MAPTARGET~N07.4

447562003~MAPRULE~IFA 367511000119101 | Hereditary mesangiocapillary glomerulonephritis, type 2 (disorder) |

447562003~MAPRULE~IFA 236422008 | Fechtner syndrome (disorder) |

447562003~MAPRULE~IFA 367561000119103 | Hereditary diffuse mesangiocapillary glomerulonephritis (disorder) |

447562003~MAPPRIORITY~5

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPTARGET~Q87.8

447562003~MAPGROUP~1

447562003~MAPADVICE~IF HEREDITARY DIFFUSE MEMBRANOUS GLOMERULONEPHRITIS CHOOSE N07.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION

447562003~MAPADVICE~IF FECHTNER SYNDROME CHOOSE D69.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPTARGET~N07.5

447562003~MAPPRIORITY~9

900000000000531004~TARGETCOMPONENT~770414008

447562003~CORRELATIONID~447561005

447562003~MAPRULE~OTHERWISE TRUE

6011000124106~MAPADVICE~ALWAYS N07.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | DESCENDANTS NOT EXHAUSTIVELY MAPPED

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

447562003~MAPTARGET~D69.4

447562003~MAPADVICE~IF EPSTEIN SYNDROME CHOOSE D69.4 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPTARGET~N07.2

447562003~MAPRULE~IFA 236420000 | Alport syndrome-like hereditary nephritis (disorder) |

447562003~MAPADVICE~IF HEREDITARY DIFFUSE MESANGIAL PROLIFERATIVE GLOMERULONEPHRITIS CHOOSE N07.3 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION

900000000000508004~ACCEPTABILITYID~900000000000548007

447562003~MAPTARGET~

447562003~MAPPRIORITY~1

447562003~MAPADVICE~SOURCE SNOMED CONCEPT IS AMBIGUOUS

447562003~MAPCATEGORYID~447637006

447562003~MAPRULE~IFA 234485006 | Epstein syndrome (disorder) |

900000000000497000~MAPTARGET~XUYoI

447562003~MAPPRIORITY~7

447562003~MAPPRIORITY~3

447562003~MAPCATEGORYID~447639009

447562003~MAPADVICE~IF HEREDITARY MESANGIOCAPILLARY GLOMERULONEPHRITIS, TYPE 2 CHOOSE N07.5 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION

6011000124106~MAPPRIORITY~1

900000000000490003~VALUEID~723278000

447562003~MAPRULE~IFA 367541000119102 | Hereditary diffuse membranous glomerulonephritis (disorder) |

6011000124106~CORRELATIONID~447561005

447562003~MAPCATEGORYID~447640006

447562003~MAPADVICE~ALWAYS Q87.8

447562003~MAPPRIORITY~2

6011000124106~MAPRULE~TRUE

447562003~MAPRULE~IFA 367551000119100 | Hereditary diffuse mesangial proliferative glomerulonephritis (disorder) |

900000000000509007~ACCEPTABILITYID~900000000000549004

447562003~MAPPRIORITY~8

447562003~MAPPRIORITY~4

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/367591000119105

http://purl.bioontology.org/ontology/SNOMEDCT/36171008

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MDRGER/10008917 MDRGER CUI
http://purl.bioontology.org/ontology/SCTSPA/399340005 SCTSPA CUI
http://purl.bioontology.org/ontology/MSHFRE/D009394 MSHFRE CUI
http://purl.bioontology.org/ontology/MDRFRE/10008917 MDRFRE CUI
http://purl.bioontology.org/ontology/NDFRT/N0000002148 NDFRT CUI
http://purl.bioontology.org/ontology/MEDDRA/10008917 MEDDRA CUI
http://purl.bioontology.org/ontology/SNMI/D7-12320 SNMI CUI
http://purl.bioontology.org/ontology/MESH/D009394 MESH CUI
http://purl.bioontology.org/ontology/OMIM/MTHU031387 OMIM CUI
http://purl.bioontology.org/ontology/RCD/X30Ie RCD CUI
http://purl.bioontology.org/ontology/SNOMEDCT/399340005 NLMVS SAME_URI
http://www.radlex.org/RID/RID5296 RADLEX LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#8579 OCHV LOOM
http://www.limics.fr/ontologies/ontolurgences#NephropathieHematuriqueHereditaireAvecSurdite ONTOLURGENCES LOOM
http://www.ebi.ac.uk/efo/EFO_0004128 CCONT LOOM
http://www.ebi.ac.uk/efo/EFO_0004128 EFO LOOM
http://www.ebi.ac.uk/efo/EFO_0004128 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0005334 GCBO LOOM
http://purl.obolibrary.org/obo/MONDO_0005334 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0005334 DOVES LOOM
http://purl.obolibrary.org/obo/MONDO_0005334 KTAO LOOM
http://purl.obolibrary.org/obo/MONDO_0005334 OBA LOOM
http://radlex.org/RID/RID5296 RADLEX LOOM
http://purl.bioontology.org/ontology/SNMI/D7-12320 SNMI LOOM
http://www.gamuts.net/entity#hereditary_glomerulonephritis GAMUTS REST