Preferred Name | Hereditary nephritis | |
Synonyms |
Hereditary nephritis (disorder) Hereditary glomerulonephritis GN - Hereditary glomerulonephritis |
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ID |
http://purl.bioontology.org/ontology/SNOMEDCT/399340005 |
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Active |
1 |
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altLabel |
Hereditary nephritis (disorder) Hereditary glomerulonephritis GN - Hereditary glomerulonephritis |
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CASE SIGNIFICANCE ID |
900000000000448009 900000000000017005 |
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CTV3ID |
XUYoI |
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cui |
C0027706 |
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DEFINITION STATUS ID |
900000000000073002 |
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Effective time |
20030731 |
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Has associated morphology | ||
Has finding site | ||
INACTIVATION INDICATOR |
723278000 |
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notation |
399340005 |
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prefLabel |
Hereditary nephritis |
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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 |
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tui |
T047 |
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Type ID |
900000000000003001 900000000000013009 |
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subClassOf |
http://purl.bioontology.org/ontology/SNOMEDCT/367591000119105 |