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1003437009: agenesie van Leydig-cel door volledige inactivatie van receptor van luteïniserend hormoon (aandoening)


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
4168242018 Leydig cell hypoplasia due to complete LH receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168243011 Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168244017 Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4168245016 Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
12134001000146111 leydigcelhypoplasie door volledige inactivatie van receptor van luteïniserend hormoon nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12134021000146115 leydigcelhypoplasie door volledige inactivatie van LH-receptor nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12256071000146112 agenesie van Leydig-cel door volledige inactivatie van receptor van luteïniserend hormoon (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12256081000146114 agenesie van Leydig-cel door volledige inactivatie van receptor van luteïniserend hormoon nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
4164764019 This is a rare autosomal recessive genetic and endocrine syndrome, characterised by a complete 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
4283400010 This is a rare autosomal recessive genetic and endocrine syndrome, characterized by a complete 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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) Is a Leydig cell agenesis true Inferred relationship Some
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) Finding site Structure of interstitial cell of Leydig true Inferred relationship Some 1
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) Occurrence Congenital true Inferred relationship Some 1
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) Associated morphology Hypoplasia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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