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42183005: Pseudohypoparathyroidism type II (disorder)

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
70396015 Pseudohypoparathyroidism type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
779054013 Pseudohypoparathyroidism type II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3786606017 Pseudohypoparathyroidism type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core
70396015 Pseudohypoparathyroidism type II en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
779054013 Pseudohypoparathyroidism type II (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3786606017 Pseudohypoparathyroidism type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core
3446691001000117 Pseudohypoparathyreoidismus Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3446691001000117 Pseudohypoparathyreoidismus Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pseudohypoparathyroidism type II (disorder) Is a Pseudohypoparathyroidism type I A false Inferred relationship Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type II (disorder) Associated morphology Dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type II (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Finding site Musculoskeletal structure of limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Pseudohypoparathyroidism type II (disorder) Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Finding site Structure of endocrine system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pseudohypoparathyroidism type II (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pseudohypoparathyroidism type II (disorder) Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pseudohypoparathyroidism type II (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Pseudohypoparathyroidism type II (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Has interpretation Decreased true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Finding site Parathyroid structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pseudohypoparathyroidism type II (disorder) Interprets Hormone secretion true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pseudohypoparathyroidism type II (disorder) Is a Pseudohypoparathyroidism true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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