718717004: Primary immunodeficiency syndrome due to p14 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)\Primary immunodeficiency syndrome due to p14 deficiency (disorder)
• \Finding of general physiological development\Disorder of stature\Short stature disorder (disorder)\Primary immunodeficiency syndrome due to p14 deficiency (disorder)
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Primary immunodeficiency syndrome due to p14 deficiency (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Primary immunodeficiency syndrome due to p14 deficiency (disorder)
• \Disease\Disorder of immune function (disorder)\Immunodeficiency disorder\Primary immune deficiency disorder\Immunodeficiency associated with chromosomal abnormality\Primary immunodeficiency syndrome due to p14 deficiency (disorder)
• \Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Primary immunodeficiency syndrome due to p14 deficiency (disorder)
• \Disease\Developmental disorder (disorder)\Disorder of stature\Short stature disorder (disorder)\Primary immunodeficiency syndrome due to p14 deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3313317017	Primary immunodeficiency syndrome due to p14 deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3313320013	Primary immunodeficiency syndrome due to p14 deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3313321012	Primary immunodeficiency syndrome with short stature	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5401831011	Primary immunodeficiency syndrome due to p14 deficiency is characterized by short stature, hypopigmentation, coarse facies and frequent bronchopulmonary Streptococcus pneumoniae infections.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401832016	Primary immunodeficiency syndrome due to p14 deficiency is characterised by short stature, hypopigmentation, coarse facies and frequent bronchopulmonary Streptococcus pneumoniae infections.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3313317017	Primary immunodeficiency syndrome due to p14 deficiency (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3313317017	Primary immunodeficiency syndrome due to p14 deficiency (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3313320013	Primary immunodeficiency syndrome due to p14 deficiency	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3313320013	Primary immunodeficiency syndrome due to p14 deficiency	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3313321012	Primary immunodeficiency syndrome with short stature	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3313321012	Primary immunodeficiency syndrome with short stature	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3313322017	This syndrome has characteristics of short stature, hypopigmentation, coarse facies and frequent bronchopulmonary Streptococcus pneumoniae infections. To date, it has been described in four members of one family. Linkage analysis led to the identification of a homozygous deletion in the coding region of the ROBLD3 gene, resulting in reduced expression of the endosomal adaptor protein p14.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401831011	Primary immunodeficiency syndrome due to p14 deficiency is characterized by short stature, hypopigmentation, coarse facies and frequent bronchopulmonary Streptococcus pneumoniae infections.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401832016	Primary immunodeficiency syndrome due to p14 deficiency is characterised by short stature, hypopigmentation, coarse facies and frequent bronchopulmonary Streptococcus pneumoniae infections.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3386221001000117	Primäres Immundefekt-Syndrom durch LAMTOR2-Defizienz	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
934721000172113	syndrome d'immunodéficience primaire avec petite taille	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
999241000172115	syndrome d'immunodéficience primaire par déficit en p14	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
934721000172113	syndrome d'immunodéficience primaire avec petite taille	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
999241000172115	syndrome d'immunodéficience primaire par déficit en p14	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3386221001000117	Primäres Immundefekt-Syndrom durch LAMTOR2-Defizienz	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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