61808009: Multiple endocrine neoplasia, type 2 (disorder)

• SNOMED CT Concept\constatation clinique\...
• \masse d'une structure corporelle\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\...
• \Neoplasm of multiple endocrine glands\Neoplasm of uncertain behavior of multiple endocrine glands\Polyglandular activity in multiple endocrine adenomatosis\Multiple endocrine neoplasia, type 2
• \Neoplasm of uncertain behavior of endocrine gland\Neoplasm of uncertain behavior of multiple endocrine glands\Polyglandular activity in multiple endocrine adenomatosis\Multiple endocrine neoplasia, type 2
• \Disease\Genetic disease\maladie héréditaire\syndrome familial avec prédisposition aux cancers (trouble)\Multiple endocrine neoplasia, type 2
• \Disease\Genetic disease\maladie héréditaire\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Multiple endocrine neoplasia, type 2
• \Disease\néoplasme et/ou hamartome\maladie néoplasique\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Neoplasm of multiple endocrine glands\Neoplasm of uncertain behavior of multiple endocrine glands\Polyglandular activity in multiple endocrine adenomatosis\Multiple endocrine neoplasia, type 2
• \Disease\néoplasme et/ou hamartome\maladie néoplasique\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Neoplasm of uncertain behavior of endocrine gland\Neoplasm of uncertain behavior of multiple endocrine glands\Polyglandular activity in multiple endocrine adenomatosis\Multiple endocrine neoplasia, type 2
• \Disease\néoplasme et/ou hamartome\maladie néoplasique\maladie néoplasique à évolution imprévisible (trouble)\Neoplasm of uncertain behavior of endocrine gland\Neoplasm of uncertain behavior of multiple endocrine glands\Polyglandular activity in multiple endocrine adenomatosis\Multiple endocrine neoplasia, type 2
• \Disease\affection d'un système corporel\Hereditary disorder by system\Hereditary disorder of endocrine system (disorder)\Multiple endocrine neoplasia, type 2
• \Disease\affection d'un système corporel\pathologie endocrinologique\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Neoplasm of multiple endocrine glands\Neoplasm of uncertain behavior of multiple endocrine glands\Polyglandular activity in multiple endocrine adenomatosis\Multiple endocrine neoplasia, type 2
• \Disease\affection d'un système corporel\pathologie endocrinologique\Neoplasm of endocrine system (disorder)\Neoplasm of endocrine gland (disorder)\Neoplasm of uncertain behavior of endocrine gland\Neoplasm of uncertain behavior of multiple endocrine glands\Polyglandular activity in multiple endocrine adenomatosis\Multiple endocrine neoplasia, type 2
• \Disease\affection d'un système corporel\pathologie endocrinologique\Hereditary disorder of endocrine system (disorder)\Multiple endocrine neoplasia, type 2
• \Disease\affection d'un système corporel\pathologie endocrinologique\Polyglandular dysfunction AND/OR related disorders\Polyglandular dysfunction\Polyglandular activity in multiple endocrine adenomatosis\Multiple endocrine neoplasia, type 2

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
102726013	Multiple endocrine neoplasia, type 2	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
102727016	MEN, type 2	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
102728014	Sipple syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
102729018	PTC syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
102730011	Familial chromaffinomatosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
102731010	MEA, type 2	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
102732015	Multiple endocrine adenomatosis, type 2	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
449501000241115	néoplasie endocrinienne multiple type 2 (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
499128019	Sipple's syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
800911018	Multiple endocrine neoplasia, type 2 (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
885011000172117	néoplasie endocrinienne multiple type 2	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
912881000172116	NEM2 - néoplasie endocrinienne multiple type 2	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)

Expanded Value Set

Reference Sets

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Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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