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239038006: Kirman syndrome (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome

\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome

\Disease\Disorder of embryonic structure (disorder)\Congenital ectodermal defect\Ectodermal dysplasia\Kirman syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital ectodermal defect\Ectodermal dysplasia\Kirman syndrome
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital ectodermal defect\Ectodermal dysplasia\Kirman syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman 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
Kirman syndrome	Is a	Ectodermal dysplasia	true	Inferred relationship	Some
Kirman syndrome	Finding site	Skin structure	false	Inferred relationship	Some	1
Kirman syndrome	Occurrence	Congenital	false	Inferred relationship	Some
Kirman syndrome	Associated morphology	Dysplasia	true	Inferred relationship	Some	1
Kirman syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Some
Kirman syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
Kirman syndrome	Finding site	Skin structure	false	Inferred relationship	Some	1
Kirman syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
Kirman syndrome	Finding site	Skin structure	true	Inferred relationship	Some	2
Kirman syndrome	Occurrence	Congenital	true	Inferred relationship	Some	2
Kirman syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	2
Kirman syndrome	Occurrence	Congenital	false	Inferred relationship	Some	3
Kirman syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	3
Kirman syndrome	Finding site	Ectoderm structure	false	Inferred relationship	Some	3
Kirman syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Kirman syndrome	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	2
Kirman syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Kirman syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2
Kirman syndrome	Finding site	Ectoderm structure	true	Inferred relationship	Some	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
358223019	Kirman syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
628000019	Kirman syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5796221000172111	syndrome de Kirman	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
4374481000172118	syndroom van Kirman	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
4374491000172115	Kirman-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)