786037006: Familial isolated hyperparathyroidism (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of head and neck region\Finding of neck region\Disorder of neck\Disorder of parathyroid gland\Hyperparathyroidism\Primary hyperparathyroidism\Familial hyperparathyroidism\Familial isolated hyperparathyroidism
• \Functional finding\Increased hormone secretion\Hyperparathyroidism\Primary hyperparathyroidism\Familial hyperparathyroidism\Familial isolated hyperparathyroidism
• \Endocrine finding\Increased hormone secretion\Hyperparathyroidism\Primary hyperparathyroidism\Familial hyperparathyroidism\Familial isolated hyperparathyroidism
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Familial isolated hyperparathyroidism
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial isolated hyperparathyroidism
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Familial isolated hyperparathyroidism
• \Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Familial isolated hyperparathyroidism
• \Disease\Disorder of body system\Disorder of endocrine system\Disorder of parathyroid gland\Hyperparathyroidism\Primary hyperparathyroidism\Familial hyperparathyroidism\Familial isolated hyperparathyroidism
• \Disease\Disorder of neck\Disorder of parathyroid gland\Hyperparathyroidism\Primary hyperparathyroidism\Familial hyperparathyroidism\Familial isolated hyperparathyroidism

Status: current, Primitive. 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	Case insensitive	SNOMED CT core
3770072015	Familial isolated hyperparathyroidism	en	Synonym	Active	Case insensitive	SNOMED CT core
3770073013	FIHPT - familial isolated hyperparathyroidism	en	Synonym	Active	Case sensitive	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	Case sensitive	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	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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