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404043000: Familial multiple leiomyoma cutis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771970019 Familial multiple leiomyoma cutis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1783017014 Familial multiple leiomyoma cutis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1771970019 Familial multiple leiomyoma cutis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1771970019 Familial multiple leiomyoma cutis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1783017014 Familial multiple leiomyoma cutis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1783017014 Familial multiple leiomyoma cutis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
651921000274118 Familiäres multiples Leiomyom der Haut de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5266481000241110 léiomyomatose cutanée familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5266481000241110 léiomyomatose cutanée familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
651921000274118 Familiäres multiples Leiomyom der Haut de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3431581001000111 Hereditäre Leiomyomatose mit Nierenzellkrebs 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
Familial multiple leiomyoma cutis (disorder) Is a Multiple piloleiomyoma (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple leiomyoma cutis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial multiple leiomyoma cutis (disorder) Associated morphology Myomatous neoplasm false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial multiple leiomyoma cutis (disorder) Associated morphology Myomatous neoplasm false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial multiple leiomyoma cutis (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial multiple leiomyoma cutis (disorder) Associated morphology Leiomyomatous neoplasm - category false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial multiple leiomyoma cutis (disorder) Is a Familial neoplastic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple leiomyoma cutis (disorder) Associated morphology Leiomyoma, no International Classification of Diseases for Oncology subtype false Inferred relationship Existential restriction modifier (core metadata concept) 1
Familial multiple leiomyoma cutis (disorder) Is a Cutaneous leiomyoma true Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple leiomyoma cutis (disorder) Associated morphology Leiomyoma (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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