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SNOMED CT
Last uploaded:
January 16, 2025
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| Id | http://purl.bioontology.org/ontology/SNOMEDCT/371122009
http://purl.bioontology.org/ontology/SNOMEDCT/371122009
|
|---|---|
| Preferred Name | Congenital anomaly of endocrine testis |
| Synonyms |
Congenital anomaly of endocrine testis (disorder)
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | Congenital anomaly of endocrine testis (disorder)
|
|---|---|
| prefLabel | Congenital anomaly of endocrine testis
|
| Type ID |
900000000000003001
900000000000013009
|
| CASE SIGNIFICANCE ID | 900000000000448009
|
| notation | 371122009
|
| Effective time | 20020731
|
| Active | 1
|
| Has finding site | |
| Has pathological process | |
| subClassOf | |
| Semantic type UMLS property | |
| type | |
| Subset member | 447562003~MAPTARGET~E29.9
6011000124106~MAPTARGET~Q55.20
447562003~MAPRULE~TRUE
6011000124106~MAPRULE~IFA 56212008 | Leydig cell agenesis |
6011000124106~MAPPRIORITY~4
900000000000497000~MAPTARGET~XUUiZ
6011000124106~MAPTARGET~E30.1
6011000124106~MAPGROUP~1
6011000124106~MAPRULE~IFA 1003437009 | Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation |
6011000124106~MAPADVICE~IF LEYDIG CELL AGENESIS CHOOSE Q55.29 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPGROUP~1
6011000124106~MAPRULE~IFA 1003438004 | Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation |
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
447562003~MAPTARGET~Q55.2
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF LEYDIG CELL HYPOPLASIA DUE TO COMPLETE LUTEINIZING HORMONE RECEPTOR INACTIVATION CHOOSE Q55.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPADVICE~ALWAYS E29.9
6011000124106~MAPADVICE~ALWAYS Q55.20
447562003~MAPPRIORITY~1
6011000124106~MAPADVICE~IF LEYDIG CELL HYPOPLASIA DUE TO PARTIAL LUTEINIZING HORMONE RECEPTOR INACTIVATION CHOOSE Q55.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPPRIORITY~5
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPRULE~IFA 725295005 | Familial male-limited precocious puberty |
6011000124106~MAPPRIORITY~1
6011000124106~MAPTARGET~Q55.29
6011000124106~CORRELATIONID~447561005
6011000124106~MAPADVICE~IF FAMILIAL MALE-LIMITED PRECOCIOUS PUBERTY CHOOSE E30.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q55.1
6011000124106~MAPPRIORITY~3
6011000124106~MAPPRIORITY~2
6011000124106~MAPRULE~IFA 56212008 | Leydig cell agenesis (disorder) |
447562003~MAPADVICE~ALWAYS Q55.2
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|
| DEFINITION STATUS ID | 900000000000073002
|
| tui | T019
|
| CTV3ID | XUUiZ
|
| Occurs in | |
| cui | C1299568
|
| Has associated morphology |
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