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Vasculopathy, Retinal, With Cerebral Leukodystrophy MeSH Supplementary Concept Data 2023


MeSH Supplementary
Vasculopathy, Retinal, With Cerebral Leukodystrophy
Unique ID
C566007
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566007
Entry Term(s)
Cerebroretinal Vasculopathy, Hereditary
Retinopathy, Vascular, With Cerebral And Renal Involvement And Raynaud And Migraine Phenomena
Registry Number
0
Heading Mapped to
*Retinal Diseases
*Vascular Diseases
*Hereditary Central Nervous System Demyelinating Diseases
Frequency
11
Note
mutations in TREX1
Date of Entry
2012/11/05
Vasculopathy, Retinal, With Cerebral Leukodystrophy Preferred
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