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402685001: Poikiloderma (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)

\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)

\Disease\Degenerative disorder\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Atrophic condition of skin (disorder)\Poikiloderma (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1770609013 Poikiloderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1781785014 Poikiloderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5261321000241113 poïkilodermie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Poikiloderma (disorder)	Is a	Degenerative disorder	false	Inferred relationship	Some
Poikiloderma (disorder)	Associated morphology	dégénérescence	false	Inferred relationship	Some
Poikiloderma (disorder)	Is a	Atrophic condition of skin (disorder)	true	Inferred relationship	Some
Poikiloderma (disorder)	Finding site	Skin structure	false	Inferred relationship	Some	1
Poikiloderma (disorder)	Associated morphology	Poikiloderma	false	Inferred relationship	Some	1
Poikiloderma (disorder)	Finding site	Skin structure	true	Inferred relationship	Some	1
Poikiloderma (disorder)	Associated morphology	Poikiloderma	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Poikiloderma due to lichen planus (disorder)	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
poïkilodermie avec syndrome génétique ou congénital	Is a	False	Poikiloderma (disorder)	Inferred relationship	Some
Poikiloderma due to lupus erythematosus	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
Poikiloderma due to scleroderma	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
Telangiectasia caused by ionizing radiation (disorder)	Is a	False	Poikiloderma (disorder)	Inferred relationship	Some
Poikilodermatous mycosis fungoides (disorder)	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
Diffuse and macular atrophic dermatosis of Stevanovic	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
Acquired poikiloderma (disorder)	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
Rothmund-Thomson syndrome	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
PARC syndrome is a rare genetic developmental defect during embryogenesis syndrome characterized by the association of congenital poikiloderma (P), generalized alopecia (A), retrognathism (R) and cleft palate (C). There have been no further descriptions in the literature since 1990.	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
Poikiloderma caused by ionizing radiation	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
Hereditary sclerosing poikiloderma	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
Poikiloderma with neutropenia is a rare, genetic hereditary poikiloderma disorder characterized by early-onset poikiloderma (which typically begins in the extremities, progresses centripetally and eventually involves the trunk, face and ears) associated with chronic neutropenia, recurrent infections, pachyonychia and palmoplantar keratoderma. Growth and/or developmental delay and hepato- and/or splenomegaly are additional reported features.	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
Poikiloderma caused by photodynamic agent (disorder)	Is a	False	Poikiloderma (disorder)	Inferred relationship	Some
Poikiloderma of Civatte	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some
Poikilodermatomyositis	Is a	True	Poikiloderma (disorder)	Inferred relationship	Some

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1770609013	Poikiloderma (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1781785014	Poikiloderma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5261321000241113	poïkilodermie	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module