764100007: Primary intraosseous venous malformation (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Mass of body structure\Mass of soft tissue\Neoplasm of soft tissue (disorder)\Benign neoplasm of soft tissue\Congenital hemangioma\Primary intraosseous venous malformation
• \Mass of body structure\Mass of cardiovascular structure (finding)\Neoplasm of cardiovascular system\Congenital hemangioma\Primary intraosseous venous malformation
• \General finding of soft tissue\Mass of soft tissue\Neoplasm of soft tissue (disorder)\Benign neoplasm of soft tissue\Congenital hemangioma\Primary intraosseous venous malformation
• \General finding of soft tissue\Blood vessel finding\Disorder of blood vessel (disorder)\Congenital vascular disorder\Congenital hemangioma\Primary intraosseous venous malformation
• \General finding of soft tissue\Disorder of soft tissue\Lesion of soft tissue (disorder)\Neoplasm of soft tissue (disorder)\Benign neoplasm of soft tissue\Congenital hemangioma\Primary intraosseous venous malformation
• \General finding of soft tissue\Disorder of soft tissue\Disorder of blood vessel (disorder)\Congenital vascular disorder\Congenital hemangioma\Primary intraosseous venous malformation
• \Cardiovascular finding\Mass of cardiovascular structure (finding)\Neoplasm of cardiovascular system\Congenital hemangioma\Primary intraosseous venous malformation
• \Cardiovascular finding\Disorder of cardiovascular system\Congenital cardiovascular disorder (disorder)\Congenital vascular disorder\Congenital hemangioma\Primary intraosseous venous malformation
• \Cardiovascular finding\Disorder of cardiovascular system\Neoplasm of cardiovascular system\Congenital hemangioma\Primary intraosseous venous malformation
• \Cardiovascular finding\Disorder of cardiovascular system\Cardiovascular system hereditary disorder\Primary intraosseous venous malformation
• \Cardiovascular finding\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Congenital vascular disorder\Congenital hemangioma\Primary intraosseous venous malformation
• \Cardiovascular finding\Blood vessel finding\Disorder of blood vessel (disorder)\Congenital vascular disorder\Congenital hemangioma\Primary intraosseous venous malformation
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Cardiovascular system hereditary disorder\Primary intraosseous venous malformation
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Primary intraosseous venous malformation
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital cardiovascular disorder (disorder)\Congenital vascular disorder\Congenital hemangioma\Primary intraosseous venous malformation
• \Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of cardiovascular system\Congenital hemangioma\Primary intraosseous venous malformation
• \Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Neoplasm of soft tissue (disorder)\Benign neoplasm of soft tissue\Congenital hemangioma\Primary intraosseous venous malformation
• \Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Haemangioma\Congenital hemangioma\Primary intraosseous venous malformation
• \Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Haemangioma\Infantile haemangioma of rare localisation\Primary intraosseous venous malformation
• \Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Benign neoplasm of soft tissue\Congenital hemangioma\Primary intraosseous venous malformation
• \Disease\Disorder of body system\Hereditary disorder by system (disorder)\Cardiovascular system hereditary disorder\Primary intraosseous venous malformation
• \Disease\Disorder of body system\Disorder of cardiovascular system\Congenital cardiovascular disorder (disorder)\Congenital vascular disorder\Congenital hemangioma\Primary intraosseous venous malformation
• \Disease\Disorder of body system\Disorder of cardiovascular system\Neoplasm of cardiovascular system\Congenital hemangioma\Primary intraosseous venous malformation
• \Disease\Disorder of body system\Disorder of cardiovascular system\Cardiovascular system hereditary disorder\Primary intraosseous venous malformation
• \Disease\Disorder of body system\Disorder of cardiovascular system\Disorder of blood vessel (disorder)\Congenital vascular disorder\Congenital hemangioma\Primary intraosseous venous malformation
• \Disease\Disorder of soft tissue\Lesion of soft tissue (disorder)\Neoplasm of soft tissue (disorder)\Benign neoplasm of soft tissue\Congenital hemangioma\Primary intraosseous venous malformation
• \Disease\Disorder of soft tissue\Disorder of blood vessel (disorder)\Congenital vascular disorder\Congenital hemangioma\Primary intraosseous venous malformation

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3646045014	Intraosseous hemangioma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3646046010	Intraosseous haemangioma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3646047018	Primary intraosseous venous malformation (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3646048011	Osseous venous malformation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3646049015	Primary intraosseous venous malformation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5404276016	Primary intraosseous venous malformation is a rare, genetic vascular anomaly characterized by severe blood vessel expansion (most frequently within the craniofacial bones) with painless bone enlargement (usually of mandible, maxilla and/or orbital, nasal, and frontal bones), typically resulting in facial asymmetry and contour deformation. Midline abnormalities, such as diastasis recti, supraumbilical raphe, and hiatus hernia, are commonly associated. Additional features reported include gingival bleeding, ectopic tooth eruption, exophthalmos, loss of vision, nausea, and vomiting.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5404277013	Primary intraosseous venous malformation is a rare, genetic vascular anomaly characterised by severe blood vessel expansion (most frequently within the craniofacial bones) with painless bone enlargement (usually of mandible, maxilla and/or orbital, nasal, and frontal bones), typically resulting in facial asymmetry and contour deformation. Midline abnormalities, such as diastasis recti, supraumbilical raphe, and hiatus hernia, are commonly associated. Additional features reported include gingival bleeding, ectopic tooth eruption, exophthalmos, loss of vision, nausea, and vomiting.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3646045014	Intraosseous hemangioma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3646046010	Intraosseous haemangioma	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3646047018	Primary intraosseous venous malformation (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3646048011	Osseous venous malformation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3646049015	Primary intraosseous venous malformation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3646051016	A rare genetic vascular anomaly with characteristics of severe blood vessel expansion most frequently within the craniofacial bones with painless bone enlargement usually of mandibula, maxilla and/or orbital, nasal and frontal bones. This typically results in facial asymmetry and contour deformation. Midline abnormalities, such as diastasis recti, supraumbilical raphe, and hiatus hernia, are commonly associated. Additional features reported include gingival bleeding, ectopic tooth eruption, exophthalmos and loss of vision, nausea, and vomiting. There is evidence the disease is caused by homozygous mutation in the ELMO2 gene on chromosome 20q13.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5404276016	Primary intraosseous venous malformation is a rare, genetic vascular anomaly characterized by severe blood vessel expansion (most frequently within the craniofacial bones) with painless bone enlargement (usually of mandible, maxilla and/or orbital, nasal, and frontal bones), typically resulting in facial asymmetry and contour deformation. Midline abnormalities, such as diastasis recti, supraumbilical raphe, and hiatus hernia, are commonly associated. Additional features reported include gingival bleeding, ectopic tooth eruption, exophthalmos, loss of vision, nausea, and vomiting.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5404277013	Primary intraosseous venous malformation is a rare, genetic vascular anomaly characterised by severe blood vessel expansion (most frequently within the craniofacial bones) with painless bone enlargement (usually of mandible, maxilla and/or orbital, nasal, and frontal bones), typically resulting in facial asymmetry and contour deformation. Midline abnormalities, such as diastasis recti, supraumbilical raphe, and hiatus hernia, are commonly associated. Additional features reported include gingival bleeding, ectopic tooth eruption, exophthalmos, loss of vision, nausea, and vomiting.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3420301001000118	Venöse Fehlbildung, intraossäre primäre	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
926861000172119	malformation veineuse osseuse primaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1019751000172117	hémangiome intraosseux	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
926861000172119	malformation veineuse osseuse primaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
1019751000172117	hémangiome intraosseux	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3420301001000118	Venöse Fehlbildung, intraossäre primäre	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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