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715907003: Multiple endocrine neoplasia type 4 (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3304104013 Multiple endocrine neoplasia type 4 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304105014 Multiple endocrine neoplasia type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304106010 MEN (multiple endocrine neoplasia) 4 syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401161017 Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterized by parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401162012 Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterised by parathyroid and anterior pituitary tumours, possibly associated with adrenal, renal, and reproductive organ tumours. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3304104013 Multiple endocrine neoplasia type 4 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3304104013 Multiple endocrine neoplasia type 4 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304105014 Multiple endocrine neoplasia type 4 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3304105014 Multiple endocrine neoplasia type 4 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304106010 MEN (multiple endocrine neoplasia) 4 syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3304107018 A very rare form of multiple endocrine neoplasia, an inherited cancer syndrome, with parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors. Caused by heterozygous inactivating mutations in the CDKN1B gene (12p13.1-p12) encoding p27, a cyclin-dependent kinase inhibitor that acts as a negative regulator of cell cycle progression. Most cases are the result of autosomal dominant inheritance. Some cases of sporadic de novo occurrence are however reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3304108011 A very rare form of multiple endocrine neoplasia, an inherited cancer syndrome, with parathyroid and anterior pituitary tumours, possibly associated with adrenal, renal, and reproductive organ tumours. Caused by heterozygous inactivating mutations in the CDKN1B gene (12p13.1-p12) encoding p27, a cyclin-dependent kinase inhibitor that acts as a negative regulator of cell cycle progression. Most cases are the result of autosomal dominant inheritance. Some cases of sporadic de novo occurrence are however reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401161017 Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterized by parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401162012 Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterised by parathyroid and anterior pituitary tumours, possibly associated with adrenal, renal, and reproductive organ tumours. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3388931001000112 Neoplasie, endokrine multiple, Typ 4 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
933001000172119 néoplasie endocrinienne multiple type 4 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
973561000172110 MEN4 - multiple endocrine neoplasia type 4 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
933001000172119 néoplasie endocrinienne multiple type 4 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
973561000172110 MEN4 - multiple endocrine neoplasia type 4 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3388931001000112 Neoplasie, endokrine multiple, Typ 4 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterised by parathyroid and anterior pituitary tumours, possibly associated with adrenal, renal, and reproductive organ tumours. Is a Polyglandular activity in multiple endocrine adenomatosis true Inferred relationship Existential restriction modifier (core metadata concept)
Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterised by parathyroid and anterior pituitary tumours, possibly associated with adrenal, renal, and reproductive organ tumours. Associated morphology Multiple endocrine adenomas (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterised by parathyroid and anterior pituitary tumours, possibly associated with adrenal, renal, and reproductive organ tumours. Finding site Structure of multiple endocrine glands (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN, an inherited cancer syndrome, characterised by parathyroid and anterior pituitary tumours, possibly associated with adrenal, renal, and reproductive organ tumours. Is a Genetic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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