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23272008: Familial hypoceruloplasminemia (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
39063012 Familial hypoceruloplasminemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
481579015 Familial hypoceruloplasminaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
752773016 Familial hypoceruloplasminemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
39063012 Familial hypoceruloplasminemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
39063012 Familial hypoceruloplasminemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
481579015 Familial hypoceruloplasminaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
481579015 Familial hypoceruloplasminaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
752773016 Familial hypoceruloplasminemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
752773016 Familial hypoceruloplasminemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6179651000241117 hypocéruloplasminémie familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6179651000241117 hypocéruloplasminémie familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial hypoceruloplasminemia Is a Disorder of copper metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Familial hypoceruloplasminemia Finding site Body system structure false 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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