711152006: autosomaal dominante hypocalciëmie (aandoening)

SNOMED CT Concept\Clinical finding (finding)\Disease\...

\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Autosomal dominant hypocalcemia (disorder)

\Metabolic disease\Disorder of mineral metabolism\Disorder of phosphate, calcium and vitamin D metabolism\Disorder of calcium metabolism\Hypocalcemia\Autosomal dominant hypocalcemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3047510011 Autosomal dominant hypocalcemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3047511010 Autosomal dominant hypocalcemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3047512015 Autosomal dominant hypocalcaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3047513013 Familial hypocalcemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3047514019 Familial hypocalcaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3047515018 Autosomal dominant hypoparathyroidism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3047516017 Familial hypercalciuric hypocalcemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3047517014 Familial hypercalciuric hypocalcaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5907481000146114 autosomaal dominante hypocalciëmie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5907491000146111 autosomaal dominante hypocalciëmie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Autosomal dominant hypocalcemia (disorder)	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Autosomal dominant hypocalcemia (disorder)	Is a	Hypocalcemia	true	Inferred relationship	Some
Autosomal dominant hypocalcemia (disorder)	Is a	Hereditary metabolic disease	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
syndroom van hypoparathyreoïdie, perceptief gehoorverlies en nierziekte	Is a	False	Autosomal dominant hypocalcemia (disorder)	Inferred relationship	Some

This concept is not in any reference sets