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Terminology chevron_right Concepts chevron_right 1003437009

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  • Language with ID “31eb6c4e-89cc-5b8b-bcbd-85b3f2fe0cc3” doesn’t exist. Perhaps it was deleted?
1003437009
The component that hold information about this concept.
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder)
Leydig cell hypoplasia due to complete lh receptor inactivation
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder)

SCTID: 1003437009, Primitive, Active


1003437009|Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder)|
  • en Leydig cell hypoplasia due to complete lh receptor inactivation
  • en Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation
  • en Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation
  • en Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder)

1003437009 |Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder)|

<<< 56212008 |Leydig cell agenesis (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 44185004 |Structure of interstitial cell of leydig (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
Active

4168242018 - Leydig cell hypoplasia due to complete LH receptor inactivation (en) View

4168242018
en
Synonym (core metadata concept)
Leydig cell hypoplasia due to complete LH receptor inactivation
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

4168244017 - Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation (en) View

4168244017
en
Synonym (core metadata concept)
Leydig cell hypoplasia due to complete luteinising hormone receptor inactivation
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

4168245016 - Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (en) View

4168245016
en
Synonym (core metadata concept)
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

4168243011 - Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder) (en) View

4168243011
en
Fully specified name (core metadata concept)
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation (disorder)
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
True

56212008 View

56212008
Leydig cell agenesis (disorder)
Leydig cell agenesis
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (0fbb420e-f773-50a5-8b2c-25e2d012a461) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q56.1
TRUE
ALWAYS Q56.1
447561005 |Snomed ct source code to target map code correlation not specified (foundation metadata concept)|
447637006 |Map source concept is properly classified (foundation metadata concept)|
esc