237839005: Growth hormone receptor abnormality (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of general physiological development\Disorder of stature\Short stature disorder\Laron-type isolated somatotropin defect\Growth hormone receptor abnormality
• \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\Growth hormone receptor abnormality
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Laron-type isolated somatotropin defect\Growth hormone receptor abnormality
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Laron-type isolated somatotropin defect\Growth hormone receptor abnormality
• \Disease\Developmental disorder\Developmental hereditary disorder\Laron-type isolated somatotropin defect\Growth hormone receptor abnormality
• \Disease\Developmental disorder\Disorder of stature\Short stature disorder\Laron-type isolated somatotropin defect\Growth hormone receptor abnormality

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356427012	Growth hormone receptor abnormality	en	Synonym	Active	Case insensitive	SNOMED CT core
626624016	Growth hormone receptor abnormality (disorder)	en	Fully specified name	Active	Case insensitive	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

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