783098009: Short stature due to partial growth hormone receptor deficiency (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Body measurement finding\Height / growth finding\General finding of height (finding)\Disorder of stature\Short stature disorder (disorder)\Short stature co-occurrent and due to endocrine disorder (disorder)\Short stature due to partial growth hormone receptor deficiency
• \Finding of general physiological development\Disorder of stature\Short stature disorder (disorder)\Short stature co-occurrent and due to endocrine disorder (disorder)\Short stature due to partial growth hormone receptor deficiency
• \Disease\Disorder of body system\Disorder of endocrine system (disorder)\Short stature co-occurrent and due to endocrine disorder (disorder)\Short stature due to partial growth hormone receptor deficiency
• \Disease\Developmental disorder (disorder)\Disorder of stature\Short stature disorder (disorder)\Short stature co-occurrent and due to endocrine disorder (disorder)\Short stature due to partial growth hormone receptor deficiency

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3757576010	Short stature due to partial growth hormone receptor deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3757577018	Short stature due to partial growth hormone receptor deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3757578011	Short stature due to partial GHR (growth hormone receptor) deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3757579015	A rare genetic endocrine disease with characteristics of idiopathic short stature due to diminished GHR function (decreased ligand binding or reduced availability of receptor), thus resulting in partial insensitivity to growth hormone. There is evidence the disease is caused by heterozygous mutation in the growth hormone receptor gene (GHR) on chromosome 5p13-p12.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3757576010	Short stature due to partial growth hormone receptor deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3757577018	Short stature due to partial growth hormone receptor deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3757578011	Short stature due to partial GHR (growth hormone receptor) deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3757579015	A rare genetic endocrine disease with characteristics of idiopathic short stature due to diminished GHR function (decreased ligand binding or reduced availability of receptor), thus resulting in partial insensitivity to growth hormone. There is evidence the disease is caused by heterozygous mutation in the growth hormone receptor gene (GHR) on chromosome 5p13-p12.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3442541001000111	Kleinwuchs durch partiellen GHR-Mangel	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3442541001000111	Kleinwuchs durch partiellen GHR-Mangel	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

This concept is not in any reference sets

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