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237687003: Isolated growth hormone deficiency - 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
356231015 Autosomal dominant isolated somatotropin deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
356232010 Isolated growth hormone deficiency - autosomal dominant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626450013 Isolated growth hormone deficiency - autosomal dominant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3702731000052115 autosomalt dominant isolerad somatotropinbrist 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
Autosomal dominant isolated somatotropin deficiency Is a Isolated somatotropin deficiency true Inferred relationship Some
Autosomal dominant isolated somatotropin deficiency Finding site Entire endocrine gonad (body structure) false Inferred relationship Some
Autosomal dominant isolated somatotropin deficiency Finding site Pars anterior of pituitary gland false Inferred relationship Some
Autosomal dominant isolated somatotropin deficiency Interprets Nutritional deficiency (finding) false Inferred relationship Some
Autosomal dominant isolated somatotropin deficiency Finding site Structure of pars distalis of pituitary (body structure) 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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