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1304119009: mozaïekvorm van neurofibromatose type 2 (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5309369012 Mosaic neurofibromatosis type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5309370013 Mosaic neurofibromatosis type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5309371012 MNF2 - mosaic neurofibromatosis type 2 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5309372017 Mosaic NF2-related schwannomatosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
15096631000146119 mozaïekvorm van neurofibromatose type 2 (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15096641000146110 mozaïcisme van NF2 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
15096651000146113 mozaïekvorm van neurofibromatose type 2 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5309373010 A rare mosaic form of NF2-related schwannomatosis characterised by findings typical of NF2-related schwannomatosis, namely development of multiple benign nerve sheath tumours, particularly affecting the vestibular nerve. Mosaic form is caused by postzygotic pathogenic variants in NF2. In mosaic NF2-related schwannomatosis the allelic/tissue distribution of the pathogenic NF2 variant clearly suggests mosaicism. The phenotype can be milder than in NF2-related schwannomatosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5309374016 A rare mosaic form of NF2-related schwannomatosis characterized by findings typical of NF2-related schwannomatosis, namely development of multiple benign nerve sheath tumors, particularly affecting the vestibular nerve. Mosaic form is caused by postzygotic pathogenic variants in NF2. In mosaic NF2-related schwannomatosis the allelic/tissue distribution of the pathogenic NF2 variant clearly suggests mosaicism. The phenotype can be milder than in NF2-related schwannomatosis. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mosaic neurofibromatosis type 2 (disorder) Is a Neurofibromatosis type 2 true Inferred relationship Some
Mosaic neurofibromatosis type 2 (disorder) Occurrence Congenital true Inferred relationship Some 2
Mosaic neurofibromatosis type 2 (disorder) Finding site Structure of nervous system (body structure) true Inferred relationship Some 2
Mosaic neurofibromatosis type 2 (disorder) Associated morphology Neurofibromatosis true Inferred relationship Some 2
Mosaic neurofibromatosis type 2 (disorder) Occurrence Congenital true Inferred relationship Some 3
Mosaic neurofibromatosis type 2 (disorder) Finding site Skin structure true Inferred relationship Some 3
Mosaic neurofibromatosis type 2 (disorder) Associated morphology Neurofibromatosis true Inferred relationship Some 3
Mosaic neurofibromatosis type 2 (disorder) Finding site Vestibulocochlear nerve structure true Inferred relationship Some 1
Mosaic neurofibromatosis type 2 (disorder) Associated morphology Schwannoma true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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