MeSH Browser

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
Heading Mapped to: *Retinal Diseases; *Vascular Diseases; *Hereditary Central Nervous System Demyelinating Diseases
Frequency: 12
Note: mutations in TREX1
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Vasculopathy, Retinal, With Cerebral Leukodystrophy MeSH Supplementary Concept Data 2024