1177118004: Laminopathy with premature aging (disorder)

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)

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)
\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)

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)
\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)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Premature aging syndrome (disorder)\Laminopathy with premature aging (disorder)

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

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Oct 2021. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Laminopathy with premature aging (disorder)	Is a	Premature aging syndrome (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Laminopathy with premature aging (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Laminopathy with premature aging (disorder)	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hutchinson-Gilford syndrome	Is a	True	Laminopathy with premature aging (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Lethal tight skin contracture syndrome (disorder)	Is a	True	Laminopathy with premature aging (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
LMNA-related cardiocutaneous progeria syndrome	Is a	True	Laminopathy with premature aging (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Atypical Werner syndrome (disorder)	Is a	True	Laminopathy with premature aging (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
4643441014	Laminopathy with premature aging (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4643442019	Laminopathy with premature aging	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4643443012	Laminopathy with premature ageing	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4643441014	Laminopathy with premature aging (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4643442019	Laminopathy with premature aging	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4643443012	Laminopathy with premature ageing	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6327851000241117	laminopathie avec vieillissement prématuré	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6327851000241117	laminopathie avec vieillissement prématuré	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module