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715218009: hyperparathyroïdie primitive sévère néonatale (trouble)


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
746851000241118 hyperparathyroïdie primitive sévère néonatale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
921681000172116 NSHPT - neonatal severe primary hyperparathyroidism fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
990151000172117 hyperparathyroïdie primitive sévère néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal severe primary hyperparathyroidism (disorder) est un(e) (attribut) Neonatal hyperparathyroidism true Inferred relationship Some
Neonatal severe primary hyperparathyroidism (disorder) survenue (attribut) néonatal true Inferred relationship Some 2
Neonatal severe primary hyperparathyroidism (disorder) localisation d'une constatation (attribut) Parathyroid structure true Inferred relationship Some 3
Neonatal severe primary hyperparathyroidism (disorder) est défini par la manifestation de (attribut) Increased hormone secretion false Inferred relationship Some
Neonatal severe primary hyperparathyroidism (disorder) interprète (attribut) Hormone secretion true Inferred relationship Some 1
Neonatal severe primary hyperparathyroidism (disorder) a pour interprétation (attribut) augmenté true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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