FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

702627001: Aplasia of testicle (disorder)


Status: current, Defined. Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3005306013 Aplasia of testicle en Synonym Active Case insensitive SNOMED CT core
3005325011 Aplasia of testicle (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3005341012 Congenital aplasia of testis en Synonym Active Case insensitive SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aplasia of testicle Pathological process Pathological developmental process true Inferred relationship Some 1
Aplasia of testicle Is a Monorchism false Inferred relationship Some
Aplasia of testicle Is a Absent testicle (congenital) true Inferred relationship Some
Aplasia of testicle Is a Congenital anomaly of testis false Inferred relationship Some
Aplasia of testicle Occurrence Congenital true Inferred relationship Some 1
Aplasia of testicle Associated morphology Aplasia true Inferred relationship Some 1
Aplasia of testicle Finding site Testis structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital absence of left testis Is a False Aplasia of testicle Inferred relationship Some
Congenital absence of right testis Is a False Aplasia of testicle Inferred relationship Some
Congenital absence of germinal epithelium of testes Is a True Aplasia of testicle Inferred relationship Some
Agenesis of testis Is a True Aplasia of testicle Inferred relationship Some
Absent testicle (congenital) Is a False Aplasia of testicle Inferred relationship Some
Congenital absence of both testes Is a False Aplasia of testicle Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start