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765282004: Male infertility with oligozoospermia due to single gene mutation (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3657755015 Male infertility with oligozoospermia due to single gene mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3657756019 Male infertility with oligozoospermia due to single gene mutation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4651792018 Male infertility with oligospermia due to single gene mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3657757011 A rare genetic male infertility due to oligozoospermia (number of sperm in the ejaculate inferior to 15 million/mL) resulting from a mutation in a single gene known to cause oligozoospermia. Sperm morphology may be normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3657755015 Male infertility with oligozoospermia due to single gene mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3657756019 Male infertility with oligozoospermia due to single gene mutation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4651792018 Male infertility with oligospermia due to single gene mutation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3657757011 A rare genetic male infertility due to oligozoospermia (number of sperm in the ejaculate inferior to 15 million/mL) resulting from a mutation in a single gene known to cause oligozoospermia. Sperm morphology may be normal. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
6357031000241115 infertilité masculine avec oligozoospermie due à une mutation monogénique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6357041000241113 infertilité chez l'homme avec oligozoospermie due à la mutation d'un seul gène fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6357031000241115 infertilité masculine avec oligozoospermie due à une mutation monogénique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6357041000241113 infertilité chez l'homme avec oligozoospermie due à la mutation d'un seul gène fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Male infertility with oligozoospermia due to single gene mutation (disorder) Due to Chromosomal disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Male infertility with oligozoospermia due to single gene mutation (disorder) Is a Male reproductive finding (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Male infertility with oligozoospermia due to single gene mutation (disorder) Interprets Male reproductive function true Inferred relationship Existential restriction modifier (core metadata concept) 4
Male infertility with oligozoospermia due to single gene mutation (disorder) Is a Male infertility of chromosomal origin false Inferred relationship Existential restriction modifier (core metadata concept)
Male infertility with oligozoospermia due to single gene mutation (disorder) Is a Male genital organ disorder associated with another disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Male infertility with oligozoospermia due to single gene mutation (disorder) Is a Oligozoospermia true Inferred relationship Existential restriction modifier (core metadata concept)
Male infertility with oligozoospermia due to single gene mutation (disorder) Interprets Concentration of spermatozoa true Inferred relationship Existential restriction modifier (core metadata concept) 1
Male infertility with oligozoospermia due to single gene mutation (disorder) Finding site Male genital organ structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Male infertility with oligozoospermia due to single gene mutation (disorder) Has interpretation Decreased true Inferred relationship Existential restriction modifier (core metadata concept) 1
Male infertility with oligozoospermia due to single gene mutation (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Male infertility with oligozoospermia due to single gene mutation (disorder) Is a Disorder of male genital organ true Inferred relationship Existential restriction modifier (core metadata concept)
Male infertility with oligozoospermia due to single gene mutation (disorder) Due to Genetic mutation (finding) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Male infertility with oligozoospermia due to single gene mutation (disorder) Is a Male infertility of genetic origin (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Male infertility with oligozoospermia due to single gene mutation (disorder) Interprets Fertility, function (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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