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239038006: Kirman syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

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

\General finding of soft tissue\Skin finding\Disorder of skin\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 of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome

\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Kirman syndrome

\Disease\Disorder of embryonic structure\Congenital ectodermal defect\Ectodermal dysplasia\Kirman syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\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\Congenital malformation\Congenital ectodermal defect\Ectodermal dysplasia\Kirman syndrome
\Disease\Congenital disease\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 of skin\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. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

358223019 Kirman syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

628000019 Kirman syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Kirman syndrome	Is a	Ectodermal dysplasia	true	Inferred relationship	Existential restriction modifier
Kirman syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Kirman syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Kirman syndrome	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	1
Kirman syndrome	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier
Kirman syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Kirman syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	1
Kirman syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	1
Kirman syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	2
Kirman syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Kirman syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Kirman syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Kirman syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	3
Kirman syndrome	Finding site	Ectoderm structure	false	Inferred relationship	Existential restriction modifier	3
Kirman syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Kirman syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	2
Kirman syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Kirman syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Kirman syndrome	Finding site	Ectoderm structure	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
358223019	Kirman syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
628000019	Kirman syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module