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SNOMED CT, US Edition
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/SNOMEDCT/93261006
http://purl.bioontology.org/ontology/SNOMEDCT/93261006
|
|---|---|
| Preferred Name | Congenital hypoplasia of gonad |
| Synonyms |
Congenital hypoplasia of gonad (disorder)
Congenital small gonad
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| prefLabel | Congenital hypoplasia of gonad
|
|---|---|
| altLabel |
Congenital hypoplasia of gonad (disorder)
Congenital small gonad
|
| Type ID |
900000000000003001
900000000000013009
|
| Semantic type UMLS property | |
| Has finding site | |
| Effective time | 20020131
|
| cui | C0685832
|
| Has pathological process | |
| CTV3ID | XUNwT
|
| DEFINITION STATUS ID | 900000000000073002
|
| CASE SIGNIFICANCE ID | 900000000000448009
|
| Occurs in | |
| tui | T019
|
| Active | 1
|
| Has associated morphology | |
| notation | 93261006
|
| type | |
| subClassOf | |
| Subset member | 6011000124106~MAPADVICE~IF MENTAL RETARDATION, DWARFISM, AND GONADAL HYPOPLASIA DUE TO XERODERMA PIGMENTOSA CHOOSE Q82.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~11
6011000124106~MAPRULE~IFA 70550008 | Streak ovary |
6011000124106~MAPTARGET~Q55.8
6011000124106~MAPADVICE~IF MENTAL RETARDATION, DWARFISM, AND GONADAL HYPOPLASIA DUE TO XERODERMA PIGMENTOSA CHOOSE E34.3 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF MALE CHOOSE Q55.1 | MAP IS CONTEXT DEPENDENT FOR GENDER
447562003~MAPRULE~TRUE
6011000124106~MAPADVICE~IF MENTAL RETARDATION, DWARFISM, AND GONADAL HYPOPLASIA DUE TO XERODERMA PIGMENTOSA CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPADVICE~IF CONGENITAL HYPOPLASIA OF TESTIS CHOOSE Q55.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q50.32
447562003~MAPADVICE~ALWAYS Q55.1
447562003~MAPRULE~IFA 248153007 | Male (finding) |
6011000124106~MAPRULE~IFA 56212008 | Leydig cell agenesis |
6011000124106~MAPPRIORITY~7
6011000124106~MAPRULE~IFA 414673004 | Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa (disorder) | AND IFA 248153007 | Male (finding) |
6011000124106~MAPPRIORITY~4
6011000124106~MAPADVICE~IF DE SANCTIS-CACCHIONE SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPTARGET~Q50.3
6011000124106~MAPRULE~IFA 248153007 | Male (finding) |
6011000124106~MAPRULE~IFA 15932141000119107 | Right streak ovary |
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPRULE~IFA 84814009 | Streak gonad |
6011000124106~MAPADVICE~IF STREAK GONAD AND IF MALE CHOOSE Q55.1 | MAP IS CONTEXT DEPENDENT FOR GENDER
6011000124106~MAPADVICE~IF FEMALE CHOOSE Q50.39 | MAP IS CONTEXT DEPENDENT FOR GENDER
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPTARGET~Q52.8
6011000124106~MAPADVICE~IF CONGENITAL HYPOPLASIA OF OVARY CHOOSE Q50.39 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPRULE~IFA 1003437009 | Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation |
6011000124106~MAPPRIORITY~10
6011000124106~MAPADVICE~IF STREAK OVARY CHOOSE Q50.32 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPADVICE~IF MENTAL RETARDATION, DWARFISM, AND GONADAL HYPOPLASIA DUE TO XERODERMA PIGMENTOSA AND IF MALE CHOOSE Q55.8 | MAP IS CONTEXT DEPENDENT FOR GENDER
6011000124106~MAPPRIORITY~15
6011000124106~MAPADVICE~IF LEYDIG CELL AGENESIS CHOOSE Q55.29 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~8
6011000124106~MAPADVICE~IF DE SANCTIS-CACCHIONE SYNDROME AND IF MALE CHOOSE Q55.8 | MAP IS CONTEXT DEPENDENT FOR GENDER
447562003~MAPADVICE~IF MALE CHOOSE Q55.1 | MAP IS CONTEXT DEPENDENT FOR GENDER
6011000124106~MAPPRIORITY~12
900000000000508004~ACCEPTABILITYID~900000000000549004
900000000000497000~MAPTARGET~XUNwT
447562003~MAPGROUP~1
6011000124106~MAPRULE~IFA 1003438004 | Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation |
6011000124106~MAPTARGET~F79
447562003~CORRELATIONID~447561005
6011000124106~MAPADVICE~IF DE SANCTIS-CACCHIONE SYNDROME CHOOSE Q82.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPRULE~OTHERWISE TRUE
6011000124106~MAPTARGET~E34.3
6011000124106~MAPRULE~IFA 85437001 | Congenital hypoplasia of testis |
6011000124106~MAPRULE~IFA 414673004 | De Sanctis-Cacchione syndrome |
6011000124106~MAPADVICE~IF TESTICULAR REGRESSION SYNDROME CHOOSE Q55.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPTARGET~Q50.39
900000000000508004~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~IF MENTAL RETARDATION, DWARFISM, AND GONADAL HYPOPLASIA DUE TO XERODERMA PIGMENTOSA AND IF FEMALE CHOOSE Q52.8 | MAP IS CONTEXT DEPENDENT FOR GENDER
447562003~MAPTARGET~
6011000124106~MAPADVICE~IF LEYDIG CELL HYPOPLASIA DUE TO COMPLETE LUTEINIZING HORMONE RECEPTOR INACTIVATION CHOOSE Q55.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPRULE~IFA 248152002 | Female (finding) |
6011000124106~MAPRULE~IFA 53599007 | Testicular regression syndrome |
447562003~MAPPRIORITY~1
6011000124106~MAPADVICE~IF LEFT STREAK OVARY CHOOSE Q50.32 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPTARGET~Q82.1
6011000124106~MAPRULE~IFA 84814009 | Streak gonad | AND IFA 248153007 | Male (finding) |
6011000124106~MAPADVICE~IF LEYDIG CELL HYPOPLASIA DUE TO PARTIAL LUTEINIZING HORMONE RECEPTOR INACTIVATION CHOOSE Q55.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~14
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~IFA 84814009 | Streak gonad | AND IFA 248152002 | Female (finding) |
6011000124106~MAPADVICE~IF STREAK GONAD AND IF FEMALE CHOOSE Q50.32 | MAP IS CONTEXT DEPENDENT FOR GENDER
6011000124106~MAPRULE~IFA 414673004 | Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa (disorder) | AND IFA 248152002 | Female (finding) |
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPPRIORITY~5
6011000124106~MAPRULE~IFA 414673004 | De Sanctis-Cacchione syndrome | AND IFA 248152002 | Female (finding) |
6011000124106~MAPGROUP~4
6011000124106~MAPADVICE~IF DE SANCTIS-CACCHIONE SYNDROME AND IF FEMALE CHOOSE Q52.8 | MAP IS CONTEXT DEPENDENT FOR GENDER
6011000124106~MAPPRIORITY~9
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPRULE~IFA 15932181000119102 | Left streak ovary |
447562003~MAPPRIORITY~3
447562003~MAPTARGET~Q55.1
447562003~MAPCATEGORYID~447639009
6011000124106~MAPPRIORITY~13
6011000124106~MAPPRIORITY~1
6011000124106~MAPRULE~IFA 85437001 | Congenital hypoplasia of testis (disorder) |
6011000124106~MAPTARGET~Q55.29
6011000124106~MAPPRIORITY~6
447562003~MAPADVICE~IF FEMALE CHOOSE Q50.3 | MAP IS CONTEXT DEPENDENT FOR GENDER
6011000124106~CORRELATIONID~447561005
6011000124106~MAPADVICE~IF RIGHT STREAK OVARY CHOOSE Q50.32 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPPRIORITY~2
6011000124106~MAPTARGET~Q55.1
6011000124106~MAPRULE~IFA 93279005 | Congenital hypoplasia of ovary |
6011000124106~MAPRULE~IFA 414673004 | De Sanctis-Cacchione syndrome | AND IFA 248153007 | Male (finding) |
6011000124106~MAPGROUP~3
6011000124106~MAPADVICE~IF DE SANCTIS-CACCHIONE SYNDROME CHOOSE E34.3 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~3
6011000124106~MAPRULE~IFA 414673004 | Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa (disorder) |
6011000124106~MAPRULE~IFA 248152002 | Female (finding) |
900000000000509007~ACCEPTABILITYID~900000000000549004
6011000124106~MAPPRIORITY~2
447562003~MAPCATEGORYID~447638001
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