237838002: Growth hormone receptor absent (disorder)

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

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
356426015	Growth hormone receptor absent	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
626622017	Growth hormone receptor absent (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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