238870004: Hutchinson-Gilford-syndroom (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome
\Disease\Disorder of foetus and/or newborn\Congenital disease (disorder)\Inborn error of metabolism\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)\Hutchinson-Gilford syndrome

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hutchinson-Gilford syndrome	Is a	Progeria	false	Inferred relationship	Some
Hutchinson-Gilford syndrome	Finding site	Skin structure	true	Inferred relationship	Some	2
Hutchinson-Gilford syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Hutchinson-Gilford syndrome	Is a	Premature aging syndrome (disorder)	false	Inferred relationship	Some
Hutchinson-Gilford syndrome	Is a	Laminopathy with premature aging (disorder)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Metageria	Is a	False	Hutchinson-Gilford syndrome	Inferred relationship	Some

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
357996013	Hutchinson-Gilford syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
357997016	Progeria syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
357998014	Premature senility syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
627809017	Hutchinson-Gilford syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
1784924019	Progeria	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
376091000146117	progeria	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
376101000146112	syndroom van Hutchinson-Gilford	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
10668461000146111	Hutchinson-Gilford-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
10668471000146117	Hutchinson-Gilford-syndroom (aandoening)	nl	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
9384501000146114	Zeldzame aangeboren ziekte die vroegtijdige en versnelde veroudering veroorzaakt, waardoor kinderen het uiterlijk en de fysionomie van ouderen krijgen en jong sterven.	nl	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)