42183005: Pseudohypoparathyroidism type II (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of head and neck region\Finding of neck region\Disorder of neck\Disorder of parathyroid gland\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type II
• \Functional finding\Decline in functional status\Decreased hormone secretion\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type II
• \Endocrine finding\Decreased hormone secretion\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type II
• \Disease\Disorder of body system\Disorder of endocrine system\Disorder of parathyroid gland\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type II
• \Disease\Disorder of neck\Disorder of parathyroid gland\Hypoparathyroidism\Pseudohypoparathyroidism\Pseudohypoparathyroidism type II
• \Disease\Metabolic disease\Disorder of mineral metabolism\Disorder of phosphate, calcium and vitamin D metabolism\Disorder of calcium metabolism\Hypocalcaemia\Pseudohypoparathyroidism\Pseudohypoparathyroidism type II

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3786606017	Pseudohypoparathyroidism type 2	en	Synonym	Active	Case insensitive	SNOMED CT core
70396015	Pseudohypoparathyroidism type II	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
779054013	Pseudohypoparathyroidism type II (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3786605018	A type of pseudohypoparathyroidism with characteristics of resistance to parathyroid hormone (PTH), which manifests with hypocalcaemia, hyperphosphataemia and elevated PTH levels, absence of Albright's hereditary osteodystrophy and normal expression of the Gs protein with a normal urinary cAMP response. To date no specific genetic alteration responsible for this disorder has been detected. It has been hypothesised that in most cases it may be an acquired defect secondary to vitamin D deficiency such as in misdiagnosed secondary renal hyperparathyroidism.	en	Definition	Active	Case sensitive	SNOMED CT core
3786607014	A type of pseudohypoparathyroidism with characteristics of resistance to parathyroid hormone (PTH), which manifests with hypocalcemia, hyperphosphatemia and elevated PTH levels, absence of Albright's hereditary osteodystrophy and normal expression of the Gs protein with a normal urinary cAMP response. To date no specific genetic alteration responsible for this disorder has been detected. It has been hypothesized that in most cases it may be an acquired defect secondary to vitamin D deficiency such as in misdiagnosed secondary renal hyperparathyroidism.	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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