Autosomal recessive hereditary disorder
Congenital anomaly of endocrine testis
Congenital connective tissue disorder
Congenital hypoplasia of testis
Connective tissue hereditary disorder
Developmental hereditary disorder
Hereditary disorder of endocrine system
Reproductive system hereditary disorder
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Leydig cell agenesis (disorder)
Leydig cell agenesis
Leydig cell hypoplasia
Leydig cell dysgenesis
Gonadotrophin unresponsiveness syndrome
Gonadotropin unresponsiveness syndrome
Id56212008
StatusDefined
Associated morphologyHypoplasia
Finding siteStructure of interstitial cell of Leydig
OccurrenceCongenital
Pathological processPathological developmental process
SNOMED CT to Orphanet simple map
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetQ99.1
Term46,XX echte hermafrodiet
SNOMED CT to ICD-10 extended map
TargetQ55.0
RuleTRUE
AdviceALWAYS Q55.0
CorrelationSNOMED CT source code to target map code correlation not specified
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Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation