782167001: Stewart-Morel-Morgagni-syndroom (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of head region\Hyperostosis interna frontalis\Stewart-Morel-Morgagni syndrome (disorder)
\Head finding (finding)\Skull finding\Hyperostosis of skull (finding)\Hyperostosis interna frontalis\Stewart-Morel-Morgagni syndrome (disorder)
\Head finding (finding)\Skull finding\Disorder of skull (disorder)\Stewart-Morel-Morgagni syndrome (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of skull (disorder)\Stewart-Morel-Morgagni syndrome (disorder)

\Musculoskeletal finding\Bone finding\Skull finding\Hyperostosis of skull (finding)\Hyperostosis interna frontalis\Stewart-Morel-Morgagni syndrome (disorder)
\Musculoskeletal finding\Bone finding\Skull finding\Disorder of skull (disorder)\Stewart-Morel-Morgagni syndrome (disorder)
\Musculoskeletal finding\Bone finding\Disorder of bone (disorder)\Hypertrophy of bone\Stewart-Morel-Morgagni syndrome (disorder)
\Musculoskeletal finding\Bone finding\Disorder of bone (disorder)\Disorder of skull (disorder)\Stewart-Morel-Morgagni syndrome (disorder)
\Musculoskeletal finding\Bone finding\Disorder of bone (disorder)\Metabolic bone disease\Stewart-Morel-Morgagni syndrome (disorder)
\Musculoskeletal finding\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Stewart-Morel-Morgagni syndrome (disorder)
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Hypertrophy of bone\Stewart-Morel-Morgagni syndrome (disorder)
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of skull (disorder)\Stewart-Morel-Morgagni syndrome (disorder)
\Musculoskeletal finding\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Metabolic bone disease\Stewart-Morel-Morgagni syndrome (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Stewart-Morel-Morgagni syndrome (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of musculoskeletal system\Stewart-Morel-Morgagni syndrome (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system\Hereditary disorder of musculoskeletal system\Stewart-Morel-Morgagni syndrome (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Hypertrophy of bone\Stewart-Morel-Morgagni syndrome (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Disorder of skull (disorder)\Stewart-Morel-Morgagni syndrome (disorder)
\Disease\Disorder of body system\Disorder of musculoskeletal system\Disorder of skeletal system\Disorder of bone (disorder)\Metabolic bone disease\Stewart-Morel-Morgagni syndrome (disorder)
\Disease\Disorder of head (disorder)\Disorder of skull (disorder)\Stewart-Morel-Morgagni syndrome (disorder)
\Disease\Metabolic disease\Metabolic bone disease\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

7001671000146112 syndroom van Stewart-Morel-Morgagni nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

7498471000146112 hyperostosis frontalis interna nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

10672411000146119 Stewart-Morel-Morgagni-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

10672421000146112 Stewart-Morel-Morgagni-syndroom (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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
Stewart-Morel-Morgagni syndrome (disorder)	Is a	Hereditary metabolic disease	false	Inferred relationship	Some

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets