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45639009: Hereditary cerebral amyloid angiopathy, Icelandic type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2011. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
76100015 Hereditary cerebral amyloid angiopathy, Icelandic type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
76101016 Amyloidosis VI en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
76103018 Iceland type amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
494297014 Icelandic type amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
494300016 Hereditary cerebral haemorrhage with amyloidosis - Icelandic type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494303019 Hereditary cerebral hemorrhage with amyloidosis - Icelandic type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
782900016 Hereditary cerebral amyloid angiopathy, Icelandic type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3973211010 Hereditary cystatin C amyloid angiopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
76100015 Hereditary cerebral amyloid angiopathy, Icelandic type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
76101016 Amyloidosis VI en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
76102011 Autosomal dominant cerebrovascular amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
76103018 Iceland type amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
76104012 Familial cerebral hemorrhage, amyloid type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
76105013 Hereditary cerebral hemorrhage with amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
76106014 HCHWA en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
76107017 Hereditary cerebral angiopathic amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494295018 Familial cerebral amyloid angiopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494296017 Hereditary central nervous system amyloid angiopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494297014 Icelandic type amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
494298016 Familial cerebral haemorrhage, amyloid type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494299012 Hereditary cerebral haemorrhage with amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494300016 Hereditary cerebral haemorrhage with amyloidosis - Icelandic type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494301017 HCHWA - Hereditary cerebral haemorrhage with amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
494302012 HCHWA - Hereditary cerebral hemorrhage with amyloidosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
494302012 HCHWA - Hereditary cerebral hemorrhage with amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
494303019 Hereditary cerebral hemorrhage with amyloidosis - Icelandic type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
782900016 Hereditary cerebral amyloid angiopathy, Icelandic type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3973211010 Hereditary cystatin C amyloid angiopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3390101001000115 ACys-Amyloidose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3390101001000115 ACys-Amyloidose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Localized hereditary amyloidosis (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Cerebrovascular amyloidosis false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Cerebral amyloid angiopathy false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Finding site Structure of cerebral artery false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Disorder of artery (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Finding site Cerebrovascular system structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary cerebral amyloid angiopathy, Icelandic type Associated morphology Focal amyloid false Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Systemic arterial finding false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary cerebral amyloid angiopathy, Icelandic type Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary cerebral amyloid angiopathy, Icelandic type Finding site Intracranial vascular structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary cerebral amyloid angiopathy, Icelandic type Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary cerebral amyloid angiopathy, Icelandic type Associated morphology Focal amyloid true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary cerebral amyloid angiopathy, Icelandic type Finding site Cerebrovascular system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Hereditary cerebral hemorrhage with amyloidosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Cerebral hemorrhage true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Is a Chronic brain syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary cerebral amyloid angiopathy, Icelandic type Associated morphology Hemorrhage true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary cerebral amyloid angiopathy, Icelandic type Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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