786037006: Familial isolated hyperparathyroidism (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos d'une région de la tête et du cou\Finding of neck region\affection du cou\affection de la glande parathyroïde (trouble)\Hyperparathyroidism\hyperparathyroïdie primaire\Familial hyperparathyroidism\Familial isolated hyperparathyroidism (disorder)
• \constatation fonctionnelle\Increased hormone secretion\Hyperparathyroidism\hyperparathyroïdie primaire\Familial hyperparathyroidism\Familial isolated hyperparathyroidism (disorder)
• \Endocrine finding\Increased hormone secretion\Hyperparathyroidism\hyperparathyroïdie primaire\Familial hyperparathyroidism\Familial isolated hyperparathyroidism (disorder)
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Familial isolated hyperparathyroidism (disorder)
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial isolated hyperparathyroidism (disorder)
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Familial isolated hyperparathyroidism (disorder)
• \Disease\affection d'un système corporel\pathologie endocrinologique\Hereditary disorder of endocrine system (disorder)\Familial isolated hyperparathyroidism (disorder)
• \Disease\affection d'un système corporel\pathologie endocrinologique\affection de la glande parathyroïde (trouble)\Hyperparathyroidism\hyperparathyroïdie primaire\Familial hyperparathyroidism\Familial isolated hyperparathyroidism (disorder)
• \Disease\affection du cou\affection de la glande parathyroïde (trouble)\Hyperparathyroidism\hyperparathyroïdie primaire\Familial hyperparathyroidism\Familial isolated hyperparathyroidism (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3770071010	Familial isolated hyperparathyroidism (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3770072015	Familial isolated hyperparathyroidism	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3770073013	FIHPT - familial isolated hyperparathyroidism	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3770074019	A rare hereditary familial primary hyperparathyroidism disease with characteristics of primary hyperparathyroidism due to single or multiple parathyroid tumours in at least two first-degree relatives in the absence of evidence of other endocrine disorders, tumours and/or systemic manifestations.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3770075018	A rare hereditary familial primary hyperparathyroidism disease with characteristics of primary hyperparathyroidism due to single or multiple parathyroid tumors in at least two first-degree relatives in the absence of evidence of other endocrine disorders, tumors and/or systemic manifestations.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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