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715218009: Neonatal severe primary hyperparathyroidism (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3301904011 Neonatal severe primary hyperparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3301905012 Neonatal severe primary hyperparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400803011 Neonatal severe primary hyperparathyroidism (NSHPT) is characterized by severe hypercalcemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400804017 Neonatal severe primary hyperparathyroidism (NSHPT) is characterised by severe hypercalcaemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3301904011 Neonatal severe primary hyperparathyroidism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3301904011 Neonatal severe primary hyperparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3301905012 Neonatal severe primary hyperparathyroidism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3301905012 Neonatal severe primary hyperparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3301906013 Characterized by severe hypercalcemia from birth and associated with major hyperparathyroidism. The prevalence is unknown, clinical manifestations are early and severe including respiratory distress, bone under mineralization and multiple fractures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3301962013 Characterised by severe hypercalcaemia from birth and associated with major hyperparathyroidism. The prevalence is unknown, clinical manifestations are early and severe including respiratory distress, bone under mineralisation and multiple fractures. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400803011 Neonatal severe primary hyperparathyroidism (NSHPT) is characterized by severe hypercalcemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400804017 Neonatal severe primary hyperparathyroidism (NSHPT) is characterised by severe hypercalcaemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3449611001000118 Hyperparathyroidismus, neonataler primärer schwerer de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
921681000172116 NSHPT - neonatal severe primary hyperparathyroidism fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
990151000172117 hyperparathyroïdie primitive sévère néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
921681000172116 NSHPT - neonatal severe primary hyperparathyroidism fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
990151000172117 hyperparathyroïdie primitive sévère néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3449611001000118 Hyperparathyroidismus, neonataler primärer schwerer 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
Neonatal severe primary hyperparathyroidism (NSHPT) is characterised by severe hypercalcaemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. Is a Neonatal hyperparathyroidism (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal severe primary hyperparathyroidism (NSHPT) is characterised by severe hypercalcaemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. Occurrence Neonatal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal severe primary hyperparathyroidism (NSHPT) is characterised by severe hypercalcaemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. Finding site Parathyroid structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Neonatal severe primary hyperparathyroidism (NSHPT) is characterised by severe hypercalcaemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. Has definitional manifestation Increased hormone secretion false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal severe primary hyperparathyroidism (NSHPT) is characterised by severe hypercalcaemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. Interprets Hormone secretion true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal severe primary hyperparathyroidism (NSHPT) is characterised by severe hypercalcaemia (> 3.5 mM) from birth and associated with major hyperparathyroidism. Has interpretation Increased true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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