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236799006: Congenitally impaired spermatogenesis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
354920018 Congenitally impaired spermatogenesis en Synonym Active Entire term case insensitive SNOMED CT core module
625440017 Congenitally impaired spermatogenesis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenitally impaired spermatogenesis Is a Congenital male infertility true Inferred relationship Existential restriction modifier
Congenitally impaired spermatogenesis Finding site Testis structure true Inferred relationship Existential restriction modifier 2
Congenitally impaired spermatogenesis Is a Disorder of testis true Inferred relationship Existential restriction modifier
Congenitally impaired spermatogenesis Finding site Entire subdivision of male genital system false Inferred relationship Existential restriction modifier
Congenitally impaired spermatogenesis Occurrence Congenital false Inferred relationship Existential restriction modifier
Congenitally impaired spermatogenesis Has definitional manifestation Infertile false Inferred relationship Existential restriction modifier
Congenitally impaired spermatogenesis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Congenitally impaired spermatogenesis Finding site Male genital structure true Inferred relationship Existential restriction modifier 1
Congenitally impaired spermatogenesis Interprets Reproductive function false Inferred relationship Existential restriction modifier 3
Congenitally impaired spermatogenesis Interprets Fertility, function true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Primary spermatogenic failure Is a True Congenitally impaired spermatogenesis Inferred relationship Existential restriction modifier
Oligosynaptic infertility Is a True Congenitally impaired spermatogenesis Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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