716742001: Multiple osteochondroma of long bone (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Mass of body structure\Mass of body region (finding)\Multiple osteochondroma
• \Mass of body structure\Mass of musculoskeletal structure (finding)\Neoplasm of musculoskeletal system (disorder)\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma
• \Musculoskeletal finding (finding)\Mass of musculoskeletal structure (finding)\Neoplasm of musculoskeletal system (disorder)\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma
• \Musculoskeletal finding (finding)\Bone finding\Disorder of bone (disorder)\Neoplasm of bone\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Neoplasm of musculoskeletal system (disorder)\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Hereditary disorder of musculoskeletal system\Multiple osteochondroma
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma
• \Musculoskeletal finding (finding)\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Neoplasm of bone\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Multiple osteochondroma
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Multiple osteochondroma
• \Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of musculoskeletal system (disorder)\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma
• \Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Osteochondroma\Osteochondroma of bone\Multiple osteochondroma
• \Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of musculoskeletal system\Multiple osteochondroma
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Neoplasm of musculoskeletal system (disorder)\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Hereditary disorder of musculoskeletal system\Multiple osteochondroma
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Neoplasm of skeletal system (disorder)\Neoplasm of bone\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma
• \Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Neoplasm of bone\Benign neoplasm of bone\Osteochondroma of bone\Multiple osteochondroma

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3307387017	Multiple osteochondroma of long bone (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307388010	Multiple osteochondroma of long bone	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307389019	Multiple osteochondroma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307391010	Bessel Hagen disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401393017	A primary bone disorder characterized by development of two or more cartilage capped bony outgrowths (osteochondromas) at the surface of the bones.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401394011	A primary bone disorder characterised by development of two or more cartilage capped bony outgrowths (osteochondromas) at the surface of the bones.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3307387017	Multiple osteochondroma of long bone (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3307387017	Multiple osteochondroma of long bone (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307388010	Multiple osteochondroma of long bone	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3307388010	Multiple osteochondroma of long bone	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307389019	Multiple osteochondroma	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3307389019	Multiple osteochondroma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3307391010	Bessel Hagen disease	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3307390011	The development of two or more cartilage capped bony outgrowths of the long bones.Develop and increase in size in the first decade of life, ceasing to grow when the growth plates close at puberty. The number may vary significantly within and between families. The majority are asymptomatic and located in bones that develop from cartilage, especially the long bones of the extremities, predominantly around the knee. The most important complication is malignant transformation towards secondary peripheral chondrosarcoma. Germline mutations in EXT1 or EXT2, are found in almost 90% of patients. An autosomal dominant disorder.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401393017	A primary bone disorder characterized by development of two or more cartilage capped bony outgrowths (osteochondromas) at the surface of the bones.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401394011	A primary bone disorder characterised by development of two or more cartilage capped bony outgrowths (osteochondromas) at the surface of the bones.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3442601001000110	Osteochondrome, multiple	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5477601000241113	ostéochondromatose multiple d'un os long	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5477601000241113	ostéochondromatose multiple d'un os long	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3442601001000110	Osteochondrome, multiple	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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