1197749008: Cell death inducing DFFA like effector C-related familial partial lipodystrophy (disorder)

• SNOMED CT Concept\constatation clinique\...
• \constatation à propos de la structure d'un membre\affection d'une extrémité\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \constatation à propos d'une structure du tronc\affection du tronc\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \constatation générale à propos des tissus mous\Subcutaneous tissue finding (finding)\Disorder of subcutaneous tissue (disorder)\Subcutaneous fat disorder (disorder)\lipodystrophie\Genetic lipodystrophy (disorder)\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \constatation générale à propos des tissus mous\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\Disorder of subcutaneous tissue (disorder)\Subcutaneous fat disorder (disorder)\lipodystrophie\Genetic lipodystrophy (disorder)\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \Integumentary system finding\Subcutaneous tissue finding (finding)\Disorder of subcutaneous tissue (disorder)\Subcutaneous fat disorder (disorder)\lipodystrophie\Genetic lipodystrophy (disorder)\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \Integumentary system finding\troubles tégumentaires\Hereditary disorder of the integument\CIDEC-related familial partial lipodystrophy
• \Integumentary system finding\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\Disorder of subcutaneous tissue (disorder)\Subcutaneous fat disorder (disorder)\lipodystrophie\Genetic lipodystrophy (disorder)\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \Disease\Genetic disease\Genetic lipodystrophy (disorder)\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of the integument\CIDEC-related familial partial lipodystrophy
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\CIDEC-related familial partial lipodystrophy
• \Disease\Genetic disease\maladie héréditaire\Connective tissue hereditary disorder\CIDEC-related familial partial lipodystrophy
• \Disease\Genetic disease\maladie héréditaire\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\CIDEC-related familial partial lipodystrophy
• \Disease\affection dégénérative\lipodystrophie\Genetic lipodystrophy (disorder)\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of the integument\CIDEC-related familial partial lipodystrophy
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\CIDEC-related familial partial lipodystrophy
• \Disease\affection d'un système corporel\pathologie endocrinologique\Hereditary disorder of endocrine system (disorder)\CIDEC-related familial partial lipodystrophy
• \Disease\affection d'un système corporel\troubles tégumentaires\Hereditary disorder of the integument\CIDEC-related familial partial lipodystrophy
• \Disease\affection d'un système corporel\troubles tégumentaires\affection de la peau et/ou du tissu sous-cutané\Disorder of subcutaneous tissue (disorder)\Subcutaneous fat disorder (disorder)\lipodystrophie\Genetic lipodystrophy (disorder)\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \Disease\affection d'une extrémité\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \Disease\affection du tronc\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \Disease\affection du tissu conjonctif\Connective tissue hereditary disorder\CIDEC-related familial partial lipodystrophy
• \Disease\affection du tissu conjonctif\Subcutaneous fat disorder (disorder)\lipodystrophie\Genetic lipodystrophy (disorder)\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy
• \Disease\Disorder of soft tissue\affection de la peau et/ou du tissu sous-cutané\Disorder of subcutaneous tissue (disorder)\Subcutaneous fat disorder (disorder)\lipodystrophie\Genetic lipodystrophy (disorder)\Familial partial lipodystrophy\CIDEC-related familial partial lipodystrophy

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4697896014	Cell death inducing DFFA like effector C-related familial partial lipodystrophy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4697897017	CIDEC-related familial partial lipodystrophy	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4697898010	Cell death inducing DFFA like effector C-related familial partial lipodystrophy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4697899019	FPLD5 - familial partial lipodystrophy type 5	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4697900012	A rare genetic lipodystrophy with characteristics of abnormal subcutaneous fat distribution, resulting in preservation of visceral, neck and axillary fat and absence of lower limb and gluteofemoral subcutaneous fat. Additional clinical features are acanthosis nigricans, insulin-resistant type II diabetes mellitus, dyslipidemia, and hypertension, leading to pancreatitis, hepatomegaly and hepatic steatosis.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4697901011	A rare genetic lipodystrophy with characteristics of abnormal subcutaneous fat distribution, resulting in preservation of visceral, neck and axillary fat and absence of lower limb and gluteofemoral subcutaneous fat. Additional clinical features are acanthosis nigricans, insulin-resistant type II diabetes mellitus, dyslipidaemia, and hypertension, leading to pancreatitis, hepatomegaly and hepatic steatosis.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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