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782167001: Stewart-Morel-Morgagni syndrome (disorder)


Status: current, Primitive. 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 Case sensitive SNOMED CT core
3752668012 Stewart-Morel-Morgagni syndrome en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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