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52967002: Myelofibrosis (disorder)

Status: current, 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
88121017 Myelofibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
496504011 MF - Myelofibrosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
496505012 Myelosclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
496506013 Agnogenic myeloid metaplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
791034018 Myelofibrosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
88121017 Myelofibrosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
88121017 Myelofibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
496504011 MF - Myelofibrosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
496505012 Myelosclerosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
496505012 Myelosclerosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
496506013 Agnogenic myeloid metaplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
496506013 Agnogenic myeloid metaplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
791034018 Myelofibrosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
791034018 Myelofibrosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
121171000172110 myélofibrose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
533141000172112 myelofibrosis fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
121171000172110 myélofibrose fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
533141000172112 myelofibrosis fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

7 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myelofibrosis Is a Bone marrow disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Myelofibrosis Finding site Bone marrow structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Myelofibrosis Pathological process Neoplastic process false Inferred relationship Existential restriction modifier (core metadata concept)
Myelofibrosis Associated morphology Reticulin fibrosis false Inferred relationship Existential restriction modifier (core metadata concept) 1
Myelofibrosis Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept)
Myelofibrosis Associated morphology Reticulin fibrosis true Inferred relationship Existential restriction modifier (core metadata concept) 1
Myelofibrosis Finding site Bone marrow structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Acute panmyelosis with myelofibrosis (disorder) Is a True Myelofibrosis Inferred relationship Existential restriction modifier (core metadata concept)
Myelosclerosis with myeloid metaplasia Is a True Myelofibrosis Inferred relationship Existential restriction modifier (core metadata concept)
Ischemic myelofibrosis (disorder) Is a True Myelofibrosis Inferred relationship Existential restriction modifier (core metadata concept)
Congenital neutropenia, myelofibrosis, nephromegaly syndrome (disorder) Is a True Myelofibrosis Inferred relationship Existential restriction modifier (core metadata concept)
Post-polycythaemia vera myelofibrosis Is a True Myelofibrosis Inferred relationship Existential restriction modifier (core metadata concept)
Myelofibrosis due to and following essential thrombocythemia (disorder) Is a True Myelofibrosis Inferred relationship Existential restriction modifier (core metadata concept)
Myelofibrosis caused by drug (disorder) Is a True Myelofibrosis Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Description inactivation indicator reference set

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