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1003438004: Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4168246015 Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168247012 Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168248019 Leydig cell hypoplasia due to partial LH receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168249010 Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4164767014 This is a rare autosomal recessive genetic and endocrine syndrome, characterised by a partial inability of the body to respond to luteinising hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4283399015 This is a rare autosomal recessive genetic and endocrine syndrome, characterized by a partial inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168246015 Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168247012 Leydig cell hypoplasia due to partial luteinising hormone receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168248019 Leydig cell hypoplasia due to partial LH receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168249010 Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4164767014 This is a rare autosomal recessive genetic and endocrine syndrome, characterised by a partial inability of the body to respond to luteinising hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4283399015 This is a rare autosomal recessive genetic and endocrine syndrome, characterized by a partial inability of the body to respond to luteinizing hormone (LH), a gonadotropin which is normally responsible for signalling Leydig cells of the testicles to produce testosterone. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
6327511000241119 hypoplasie des cellules de Leydig par inactivation partielle du récepteur LH (luteinizing hormone) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6327521000241114 hypoplasie des cellules de Leydig par résistance partielle à l'hormone lutéinisante fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6327531000241111 hypoplasie des cellules de Leydig par résistance partielle à l'ICSH (interstitial cell stimulating hormone) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6327511000241119 hypoplasie des cellules de Leydig par inactivation partielle du récepteur LH (luteinizing hormone) fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6327521000241114 hypoplasie des cellules de Leydig par résistance partielle à l'hormone lutéinisante fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6327531000241111 hypoplasie des cellules de Leydig par résistance partielle à l'ICSH (interstitial cell stimulating hormone) fr Synonym (core metadata concept) Active Only initial character 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
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation Is a Leydig cell agenesis true Inferred relationship Existential restriction modifier (core metadata concept)
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation Finding site Structure of interstitial cell of Leydig true Inferred relationship Existential restriction modifier (core metadata concept) 1
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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