79935000: Farber's lipogranulomatosis (disorder)

SNOMED CT Concept\Clinical finding\...

\General finding of soft tissue\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Panniculitis\Farber's lipogranulomatosis
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Inflammation of skin and/or subcutaneous tissue\Panniculitis\Farber's lipogranulomatosis
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Panniculitis\Farber's lipogranulomatosis

\Integumentary system finding\Subcutaneous tissue finding\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Panniculitis\Farber's lipogranulomatosis
\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Farber's lipogranulomatosis
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Inflammation of skin and/or subcutaneous tissue\Panniculitis\Farber's lipogranulomatosis
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Panniculitis\Farber's lipogranulomatosis

\Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Farber's lipogranulomatosis
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Farber's lipogranulomatosis
\Disease\Genetic disease\Hereditary disease\Connective tissue hereditary disorder\Farber's lipogranulomatosis
\Disease\Disorder of body system\Inflammation of specific body systems\Inflammation of skin and/or subcutaneous tissue\Panniculitis\Farber's lipogranulomatosis
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Farber's lipogranulomatosis
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Farber's lipogranulomatosis
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Inflammation of skin and/or subcutaneous tissue\Panniculitis\Farber's lipogranulomatosis
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Panniculitis\Farber's lipogranulomatosis
\Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammation of skin and/or subcutaneous tissue\Panniculitis\Farber's lipogranulomatosis
\Disease\Disorder of connective tissue\Connective tissue hereditary disorder\Farber's lipogranulomatosis
\Disease\Disorder of connective tissue\Congenital connective tissue disorder\Farber's lipogranulomatosis
\Disease\Disorder of connective tissue\Subcutaneous fat disorder\Panniculitis\Farber's lipogranulomatosis
\Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Farber's lipogranulomatosis
\Disease\Metabolic disease\Enzymopathy\Disorder of lysosomal enzyme\Farber's lipogranulomatosis
\Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid storage and metabolism\Farber's lipogranulomatosis
\Disease\Congenital disease\Congenital connective tissue disorder\Farber's lipogranulomatosis
\Disease\Congenital disease\Inborn error of metabolism\Storage disease\Disorder of lysosomal enzyme\Farber's lipogranulomatosis
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Inflammation of skin and/or subcutaneous tissue\Panniculitis\Farber's lipogranulomatosis
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of subcutaneous tissue\Subcutaneous fat disorder\Panniculitis\Farber's lipogranulomatosis

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

132623012 Farber's lipogranulomatosis en Synonym Active Entire term case sensitive SNOMED CT core module

132624018 Farber's disease en Synonym Active Entire term case sensitive SNOMED CT core module

132625017 Acid ceramidase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

132626016 Disseminated lipogranulomatosis en Synonym Active Entire term case insensitive SNOMED CT core module

132627013 Farber-Uzman syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

132628015 Acylsphingosine deacylase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

821040018 Farber's lipogranulomatosis (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

1234414010 Farber lipogranulomatosis en Synonym Active Entire term case sensitive SNOMED CT core module

1234415011 Ceramidase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

1234416012 Farber disease en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Farber's lipogranulomatosis	Is a	Disorder of lipid storage and metabolism	true	Inferred relationship	Existential restriction modifier
Farber's lipogranulomatosis	Is a	Hereditary disorder of the integument	true	Inferred relationship	Existential restriction modifier
Farber's lipogranulomatosis	Is a	Panniculitis	true	Inferred relationship	Existential restriction modifier
Farber's lipogranulomatosis	Is a	Disorder of lysosomal enzyme	true	Inferred relationship	Existential restriction modifier
Farber's lipogranulomatosis	Is a	Congenital anomaly of integument	false	Inferred relationship	Existential restriction modifier
Farber's lipogranulomatosis	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Farber's lipogranulomatosis	Finding site	Structure of subcutaneous fatty tissue	false	Inferred relationship	Existential restriction modifier	1
Farber's lipogranulomatosis	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier
Farber's lipogranulomatosis	Is a	Disorder of skin	false	Inferred relationship	Existential restriction modifier
Farber's lipogranulomatosis	Is a	Connective tissue hereditary disorder	true	Inferred relationship	Existential restriction modifier
Farber's lipogranulomatosis	Associated morphology	Focal inflammation	false	Inferred relationship	Existential restriction modifier	1
Farber's lipogranulomatosis	Is a	Congenital connective tissue disorder	true	Inferred relationship	Existential restriction modifier
Farber's lipogranulomatosis	Associated morphology	Inflammation	false	Inferred relationship	Existential restriction modifier	1
Farber's lipogranulomatosis	Associated morphology	Inflammation	false	Inferred relationship	Existential restriction modifier	1
Farber's lipogranulomatosis	Finding site	Structure of subcutaneous fatty tissue	true	Inferred relationship	Existential restriction modifier	1
Farber's lipogranulomatosis	Associated morphology	Inflammatory morphology	true	Inferred relationship	Existential restriction modifier	1
Farber's lipogranulomatosis	Occurrence	Congenital	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
132623012	Farber's lipogranulomatosis	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
132624018	Farber's disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
132625017	Acid ceramidase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
132626016	Disseminated lipogranulomatosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
132627013	Farber-Uzman syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
132628015	Acylsphingosine deacylase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
821040018	Farber's lipogranulomatosis (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
1234414010	Farber lipogranulomatosis	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
1234415011	Ceramidase deficiency	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
1234416012	Farber disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module