782167001: Stewart-Morel-Morgagni syndrome (disorder)

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

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

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

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

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

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

3420371001000114 Stewart-Morel-Morgagni-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

3420371001000114 Stewart-Morel-Morgagni-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

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

Inbound Relationships

Type

Active

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Characteristic

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Group

This concept is not in any reference sets