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Medical Subject Headings
| Id | http://purl.bioontology.org/ontology/MESH/D046589
http://purl.bioontology.org/ontology/MESH/D046589
|
|---|---|
| Preferred Name | CADASIL |
| Definitions |
A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES producing ischemic STROKE; PSEUDOBULBAR PALSY; and multiple subcortical infarcts (CEREBRAL INFARCTION). CADASIL is an acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL differs from BINSWANGER DISEASE by the presence of MIGRAINE WITH AURA and usually by the lack of history of arterial HYPERTENSION. (From Bradley et al, Neurology in Clinical Practice, 2000, p1146)
A subvariety of CADASIL characterized by the high frequency of MIGRAINE. The acronym stands for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts, Leukoencephalopathy, and Migraine.
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| Synonyms |
Dementia, Hereditary Multi Infarct Type
Dementia, Hereditary Multi-Infarct Type
CADASILM
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES producing ischemic STROKE; PSEUDOBULBAR PALSY; and multiple subcortical infarcts (CEREBRAL INFARCTION). CADASIL is an acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL differs from BINSWANGER DISEASE by the presence of MIGRAINE WITH AURA and usually by the lack of history of arterial HYPERTENSION. (From Bradley et al, Neurology in Clinical Practice, 2000, p1146) A subvariety of CADASIL characterized by the high frequency of MIGRAINE. The acronym stands for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts, Leukoencephalopathy, and Migraine. |
|---|---|
| altLabel |
Dementia, Hereditary Multi Infarct Type
Dementia, Hereditary Multi-Infarct Type
CADASILM
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
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| prefLabel | CADASIL
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| Machine permutation | 2005; see DEMENTIA, MULTI-INFARCT 2000-2004
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| HN | 2005; use DEMENTIA, MULTI-INFARCT 2000-2004
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| Mapped from | |
| type | |
| tui | T047
|
| TERMUI |
T367237
T764026
T764027
T553335
T764025
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| TH |
OMIM (2013)
NLM (2000)
NLM (2005)
GHR (2014)
NLM (2011)
ORD (2010)
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| MMR | 20190701
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| notation | D046589
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| Semantic type UMLS property | |
| Inverse of AQ |
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|
| DX | 20050101
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| cui |
C1449626
C0751587
|
| DC | 1
|
| MN |
C14.907.253.560.200.175
C14.907.253.092.477.200.100
C23.550.717.489.250.200.100
C10.228.140.300.400.203
C10.228.140.300.150.477.200.100
C14.907.253.329.249
C10.228.140.300.275.249
C16.320.129
C10.228.140.300.775.200.200.100
C23.550.513.355.250.200.100
C14.907.253.855.200.200.100
C10.228.140.380.230.124
C10.228.140.300.510.200.175
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| AQL | BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
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| MDA | 19991103
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| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |