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Ontology explorer

Medical Subject Headings (MeSH)
Version 2022-01-01
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causal interaction   diagnostic usage   ongoing research   therapeutic application
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Details for CADASIL
Medical Subject Headings (MeSH) ID
MESH:C.10.228.140.300.775.200.200.100
MESH:C.10.228.140.300.775.200.200.100 is linked to 29 enzymes:
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)
Synonyms
1. CADASIL
2. CADASILM
3. Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
4. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
5. Dementia, Hereditary Multi-Infarct Type
6. Dementia, Hereditary Multi Infarct Type
References
1. MESH: C.10.228.140.300.150.477.200.100
2. MESH: C.10.228.140.300.275.249
3. MESH: C.10.228.140.300.400.203
4. MESH: C.10.228.140.300.510.200.175
5. MESH: C.10.228.140.300.775.200.200.100
6. MESH: C.10.228.140.380.230.124
7. MESH: C.14.907.253.092.477.200.100
8. MESH: C.14.907.253.329.249
9. MESH: C.14.907.253.560.200.175
10. MESH: C.14.907.253.855.200.200.100
11. MESH: C.16.320.129
12. MESH: C.23.550.513.355.250.200.100
13. MESH: C.23.550.717.489.250.200.100
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derives from the parent element

Categories:
Causal interaction
Diagnostic usage
Ongoing research
Therapeutic application
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