461415008: Hereditary dysplasia of blood vessel (disorder)

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

\General finding of soft tissue\Blood vessel finding\Vascular disorder\Hereditary dysplasia of blood vessel (disorder)
\General finding of soft tissue\Disorder of soft tissue\Vascular disorder\Hereditary dysplasia of blood vessel (disorder)

\Cardiovascular finding\Disorder of cardiovascular system (disorder)\Cardiovascular system hereditary disorder\Hereditary dysplasia of blood vessel (disorder)
\Cardiovascular finding\Disorder of cardiovascular system (disorder)\Vascular disorder\Hereditary dysplasia of blood vessel (disorder)
\Cardiovascular finding\Blood vessel finding\Vascular disorder\Hereditary dysplasia of blood vessel (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Cardiovascular system hereditary disorder\Hereditary dysplasia of blood vessel (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Cardiovascular system hereditary disorder\Hereditary dysplasia of blood vessel (disorder)
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Cardiovascular system hereditary disorder\Hereditary dysplasia of blood vessel (disorder)
\Disease\Disorder of body system\Disorder of cardiovascular system (disorder)\Vascular disorder\Hereditary dysplasia of blood vessel (disorder)
\Disease\Disorder of soft tissue\Vascular disorder\Hereditary dysplasia of blood vessel (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2013. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2923300016 Hereditary dysplasia of blood vessel (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2923303019 Hereditary dysplasia of blood vessel en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5384521000241110 dysplasie vasculaire familiale héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary dysplasia of blood vessel (disorder)	Is a	Vascular disorder	true	Inferred relationship	Some
Hereditary dysplasia of blood vessel (disorder)	Is a	Cardiovascular system hereditary disorder	true	Inferred relationship	Some
Hereditary dysplasia of blood vessel (disorder)	Finding site	Blood vessel structure (body structure)	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Osler hemorrhagic telangiectasia syndrome	Is a	True	Hereditary dysplasia of blood vessel (disorder)	Inferred relationship	Some
angiodysplasie ostéodystrophique	Is a	False	Hereditary dysplasia of blood vessel (disorder)	Inferred relationship	Some
Idiopathic arterial calcification of infancy	Is a	True	Hereditary dysplasia of blood vessel (disorder)	Inferred relationship	Some
Arterial tortuosity syndrome (disorder)	Is a	True	Hereditary dysplasia of blood vessel (disorder)	Inferred relationship	Some
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by early onset of hypertension and multifocal stenotic lesions of various arteries (including cerebral, renal, abdominal, and coronary). Variable additional features include learning difficulties, mild facial dysmorphism, anomalies of the fingers and toes, bone fragility, and congenital heart defects.	Is a	True	Hereditary dysplasia of blood vessel (disorder)	Inferred relationship	Some

Reference Sets

Description inactivation indicator reference set