725035001: Familial partial lipodystrophy Kobberling type (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of limb structure\Disorder of extremity\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type

\Finding of trunk structure\Disorder of trunk\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type

\General finding of soft tissue\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type

\Integumentary system finding\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Familial partial lipodystrophy Kobberling type
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type

\Disease\Genetic disease\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Familial partial lipodystrophy Kobberling type
\Disease\Genetic disease\Hereditary disease\Connective tissue hereditary disorder\Familial partial lipodystrophy Kobberling type
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial partial lipodystrophy Kobberling type
\Disease\Degenerative disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Familial partial lipodystrophy Kobberling type
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Familial partial lipodystrophy Kobberling type
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
\Disease\Disorder of extremity\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
\Disease\Disorder of trunk\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
\Disease\Disorder of connective tissue\Connective tissue hereditary disorder\Familial partial lipodystrophy Kobberling type
\Disease\Disorder of connective tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Lipodystrophy\Genetic lipodystrophy\Familial partial lipodystrophy\Familial partial lipodystrophy Kobberling type

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3437152010 Familial partial lipodystrophy Kobberling type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module

3437153017 Familial partial lipodystrophy Kobberling type en Synonym Active Only initial character case insensitive SNOMED CT core module

3437154011 Familial partial lipodystrophy type 1 en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Familial partial lipodystrophy Kobberling type	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Familial partial lipodystrophy Kobberling type	Is a	Familial partial lipodystrophy	true	Inferred relationship	Existential restriction modifier
Familial partial lipodystrophy Kobberling type	Is a	Connective tissue hereditary disorder	true	Inferred relationship	Existential restriction modifier
Familial partial lipodystrophy Kobberling type	Is a	Hereditary disorder of the integument	true	Inferred relationship	Existential restriction modifier
Familial partial lipodystrophy Kobberling type	Finding site	Trunk structure	true	Inferred relationship	Existential restriction modifier	2
Familial partial lipodystrophy Kobberling type	Finding site	Limb structure	true	Inferred relationship	Existential restriction modifier	3
Familial partial lipodystrophy Kobberling type	Associated morphology	Dystrophy	true	Inferred relationship	Existential restriction modifier	4
Familial partial lipodystrophy Kobberling type	Finding site	Structure of subcutaneous fatty tissue	true	Inferred relationship	Existential restriction modifier	4
Familial partial lipodystrophy Kobberling type	Is a	Genetic lipodystrophy	false	Inferred relationship	Existential restriction modifier

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
3437152010	Familial partial lipodystrophy Kobberling type (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
3437153017	Familial partial lipodystrophy Kobberling type	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
3437154011	Familial partial lipodystrophy type 1	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module