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237657009: Hypoparathyroidism - autosomal dominant (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
356189019 Hypoparathyroidism - autosomal dominant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626417013 Hypoparathyroidism - autosomal dominant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3688611000052114 autosomalt dominant hypoparatyreoidism sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypoparathyroidism - autosomal dominant Is a Hypoparathyroidism true Inferred relationship Some
Hypoparathyroidism - autosomal dominant Finding site Parathyroid structure true Inferred relationship Some 2
Hypoparathyroidism - autosomal dominant Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
Hypoparathyroidism - autosomal dominant Interprets Nutritional deficiency (finding) false Inferred relationship Some
Hypoparathyroidism - autosomal dominant Has definitional manifestation Decreased hormone secretion false Inferred relationship Some
Hypoparathyroidism - autosomal dominant Has interpretation Decreased true Inferred relationship Some 1
Hypoparathyroidism - autosomal dominant Interprets Hormone secretion 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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