SNOMED CT

Last uploaded: August 28, 2024
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Preferred Name

Congenital hypoplasia of gonad
Synonyms

Congenital hypoplasia of gonad (disorder)

Congenital small gonad
ID

http://purl.bioontology.org/ontology/SNOMEDCT/93261006
Active

1
altLabel

Congenital hypoplasia of gonad (disorder)

Congenital small gonad
CASE SIGNIFICANCE ID

900000000000448009
CTV3ID

XUNwT
cui

C0685832
DEFINITION STATUS ID

900000000000073002
Effective time

20020131
Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/55199003
Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/43174007
Has pathological process

http://purl.bioontology.org/ontology/SNOMEDCT/308490002
notation

93261006
Occurs in

http://purl.bioontology.org/ontology/SNOMEDCT/255399007
prefLabel

Congenital hypoplasia of gonad
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
tui

T019
Type ID

900000000000003001

900000000000013009
subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/205681004
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