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254119005: Neonatal hyperparathyroidism (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
378284010 Neonatal hyperparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644967015 Neonatal hyperparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
378284010 Neonatal hyperparathyroidism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
378284010 Neonatal hyperparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644967015 Neonatal hyperparathyroidism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
644967015 Neonatal hyperparathyroidism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal hyperparathyroidism (disorder) Is a Neonatal metabolic and endocrinologic disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperparathyroidism (disorder) Is a Perinatal endocrine and metabolic disorders false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperparathyroidism (disorder) Is a Hyperparathyroidism true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperparathyroidism (disorder) Finding site Parathyroid structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Neonatal hyperparathyroidism (disorder) Occurrence Neonatal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal hyperparathyroidism (disorder) Finding site Entire endocrine gonad (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperparathyroidism (disorder) Occurrence Perinatal state false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperparathyroidism (disorder) Occurrence période périnatale false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperparathyroidism (disorder) Has definitional manifestation Increased hormone secretion false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperparathyroidism (disorder) Is a Neonatal disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal hyperparathyroidism (disorder) Has interpretation Increased true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal hyperparathyroidism (disorder) Interprets Hormone secretion true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Transient neonatal hyperparathyroidism (disorder) Is a True Neonatal hyperparathyroidism (disorder) 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. Is a True Neonatal hyperparathyroidism (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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