724179008: Laron syndrome with immunodeficiency (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of general physiological development\Disorder of stature\Short stature disorder\Laron syndrome with immunodeficiency
• \General finding of observation of patient\Body measurement finding\Height / growth finding\General finding of height\Disorder of stature\Short stature disorder\Laron syndrome with immunodeficiency
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Laron syndrome with immunodeficiency
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Laron syndrome with immunodeficiency
• \Disease\Disorder of immune function\Immunodeficiency disorder\Primary immune deficiency disorder\Combined immunodeficiency disease\Laron syndrome with immunodeficiency
• \Disease\Developmental disorder\Developmental hereditary disorder\Laron syndrome with immunodeficiency
• \Disease\Developmental disorder\Disorder of stature\Short stature disorder\Laron syndrome with immunodeficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3431583010	Laron syndrome with immunodeficiency (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
3431584016	Laron syndrome with immunodeficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3431585015	Laron-like syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3431586019	Short stature due to STAT5b (signal transducer and activator of transcription 5b) deficiency	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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