SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Aplasia of testicle

Synonyms

Aplasia of testicle (disorder)

Congenital aplasia of testis

ID

http://purl.bioontology.org/ontology/SNOMEDCT/702627001

Active

1

altLabel

Aplasia of testicle (disorder)

Congenital aplasia of testis

CASE SIGNIFICANCE ID

900000000000448009

CTV3ID

XUn30

cui

C3812404

DEFINITION STATUS ID

900000000000073002

Effective time

20140731

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/45486003

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/40689003

Has pathological process

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

notation

702627001

Occurs in

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

prefLabel

Aplasia of testicle

Subset member

447562003~MAPRULE~TRUE

6011000124106~MAPRULE~IFA 56212008 | Leydig cell agenesis |

6011000124106~MAPGROUP~1

6011000124106~MAPADVICE~IF LEYDIG CELL AGENESIS CHOOSE Q55.29 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000508004~ACCEPTABILITYID~900000000000549004

6011000124106~MAPTARGET~Q55.0

447562003~MAPGROUP~1

447562003~MAPADVICE~ALWAYS Q55.0

447562003~CORRELATIONID~447561005

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPRULE~IFA 371015003 | Congenital absence of both testes |

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~IF CONGENITAL ABSENCE OF BOTH TESTES CHOOSE Q55.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

900000000000497000~MAPTARGET~XUn30

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPADVICE~ALWAYS Q55.0

6011000124106~MAPPRIORITY~1

6011000124106~MAPTARGET~Q55.29

6011000124106~CORRELATIONID~447561005

6011000124106~MAPRULE~TRUE

6011000124106~MAPPRIORITY~3

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

6011000124106~MAPRULE~IFA 56212008 | Leydig cell agenesis (disorder) |

447562003~MAPTARGET~Q55.0

tui

T019

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/274151005

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