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Meretoja syndrome MeSH Supplementary Concept Data 2024


MeSH Supplementary
Meretoja syndrome
Unique ID
C537459
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C537459
Entry Term(s)
Amyloid cranial neuropathy with lattice corneal dystrophy
Amyloidosis 5
Amyloidosis V
Amyloidosis due to mutant gelsolin
Amyloidosis, Finnish Type
Amyloidosis, Meretoja Type
Cerebral Amyloid Angiopathy, Gsn-Related
Finnish type amyloidosis
Lattice corneal dystrophy associated with familial systemic amyloidosis
Lattice dystrophy of the cornea with hereditary generalized amyloidosis
Meretoja type amyloidosis
Meretoja's syndrome
Registry Number
0
Heading Mapped to
*Amyloidosis
*Corneal Dystrophies, Hereditary
Frequency
23
Note
PROM mutation in gelsolin
Date of Entry
2010/08/25
Revision Date
2020/09/29
Meretoja syndrome Preferred
Cerebral Amyloid Angiopathy, Gsn-Related Related
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