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236800005: Primary spermatogenic failure (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
354921019 Primary spermatogenic failure en Synonym Active Entire term case insensitive SNOMED CT core module
625441018 Primary spermatogenic failure (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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