1217517004: Autosomal recessive familial isolated hypoparathyroidism (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of head and neck region\Finding of neck region\Disorder of neck\Disorder of parathyroid gland\Hypoparathyroidism\Familial isolated hypoparathyroidism\Autosomal recessive familial isolated hypoparathyroidism
• \Functional finding\Decline in functional status\Decreased hormone secretion\Hypoparathyroidism\Familial isolated hypoparathyroidism\Autosomal recessive familial isolated hypoparathyroidism
• \Endocrine finding\Decreased hormone secretion\Hypoparathyroidism\Familial isolated hypoparathyroidism\Autosomal recessive familial isolated hypoparathyroidism
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of endocrine system\Familial isolated hypoparathyroidism\Autosomal recessive familial isolated hypoparathyroidism
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Autosomal recessive familial isolated hypoparathyroidism
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of endocrine system\Familial isolated hypoparathyroidism\Autosomal recessive familial isolated hypoparathyroidism
• \Disease\Disorder of body system\Disorder of endocrine system\Hereditary disorder of endocrine system\Familial isolated hypoparathyroidism\Autosomal recessive familial isolated hypoparathyroidism
• \Disease\Disorder of body system\Disorder of endocrine system\Disorder of parathyroid gland\Hypoparathyroidism\Familial isolated hypoparathyroidism\Autosomal recessive familial isolated hypoparathyroidism
• \Disease\Disorder of neck\Disorder of parathyroid gland\Hypoparathyroidism\Familial isolated hypoparathyroidism\Autosomal recessive familial isolated hypoparathyroidism

Status: current, Defined. Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5036557019	Autosomal recessive familial isolated hypoparathyroidism (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
5036558012	Autosomal recessive familial isolated hypoparathyroidism	en	Synonym	Active	Case insensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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