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782167001: Stewart-Morel-Morgagni syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3752667019 Stewart-Morel-Morgagni syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3752668012 Stewart-Morel-Morgagni syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4222421000052110 Stewart-Morel-Morgagnis syndrom sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Stewart-Morel-Morgagni syndrome (disorder) Is a Hyperostosis interna frontalis true Inferred relationship Some
Stewart-Morel-Morgagni syndrome (disorder) Finding site Frontal bone structure true Inferred relationship Some 1
Stewart-Morel-Morgagni syndrome (disorder) Is a Disorder of skull (disorder) true Inferred relationship Some
Stewart-Morel-Morgagni syndrome (disorder) Is a Metabolic bone disease true Inferred relationship Some
Stewart-Morel-Morgagni syndrome (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Stewart-Morel-Morgagni syndrome (disorder) Associated morphology Internal hyperostosis true Inferred relationship Some 1
Stewart-Morel-Morgagni syndrome (disorder) Is a Hypertrophy of bone true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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