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agenesie van Leydig-cel door volledige inactivatie van receptor van luteïniserend hormoon (aandoening)
agenesie van Leydig-cel door volledige inactivatie van receptor van luteïniserend hormoon
leydigcelhypoplasie door volledige inactivatie van receptor van luteïniserend hormoon
leydigcelhypoplasie door volledige inactivatie van LH-receptor
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation
Leydig cell hypoplasia due to complete LH receptor inactivation
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.
Id1003437009
StatusPrimitive
Associated morphologyhypoplasie
Finding sitestructuur van Leydig-cel
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetQ56.1
RuleTRUE
AdviceALWAYS Q56.1
CorrelationSNOMED CT source code to target map code correlation not specified