38196001: Laron-type isolated somatotropin defect (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of general physiological development\Disorder of stature\Short stature disorder\Laron-type isolated somatotropin defect
• \General finding of observation of patient\Body measurement finding\Height / growth finding\General finding of height\Disorder of stature\Short stature disorder\Laron-type isolated somatotropin defect
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Laron-type isolated somatotropin defect
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Laron-type isolated somatotropin defect
• \Disease\Developmental disorder\Developmental hereditary disorder\Laron-type isolated somatotropin defect
• \Disease\Developmental disorder\Disorder of stature\Short stature disorder\Laron-type isolated somatotropin defect

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4535149016	Laron syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
63917019	Laron-type isolated somatotropin defect	en	Synonym	Active	Case sensitive	SNOMED CT core
63918012	Laron-type dwarfism	en	Synonym	Active	Case sensitive	SNOMED CT core
63919016	Laron dwarfism	en	Synonym	Active	Case sensitive	SNOMED CT core
63920010	Laron-type pituitary dwarfism	en	Synonym	Active	Case sensitive	SNOMED CT core
771912011	Laron-type isolated somatotropin defect (disorder)	en	Fully specified name	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Australian dialect reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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