237838002: Growth hormone receptor absent (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos du développement physiologique\anomalie staturale\insuffisance staturale\Laron-type isolated somatotropin defect\Growth hormone receptor absent
• \constatation générale à propos de l'observation du patient\Body measurement finding\Height / growth finding\General finding of height\anomalie staturale\insuffisance staturale\Laron-type isolated somatotropin defect\Growth hormone receptor absent
• \Disease\Genetic disease\maladie héréditaire\Developmental hereditary disorder\Laron-type isolated somatotropin defect\Growth hormone receptor absent
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Laron-type isolated somatotropin defect\Growth hormone receptor absent
• \Disease\trouble du développement\Developmental hereditary disorder\Laron-type isolated somatotropin defect\Growth hormone receptor absent
• \Disease\trouble du développement\anomalie staturale\insuffisance staturale\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

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

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