MeSH Browser

MeSH Supplementary: Lattice Corneal Dystrophy, Type II
Unique ID: C000657784
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C000657784
Entry Term(s): Corneal Dystrophy, Lattice Type II; Familial Amyloid Polyneuropathy Type Iv; Familial Amyloidosis, Finnish Type; Gelsolin-Related Amyloidosis; Kymenlaakso Syndrome; Lattice Corneal Dystrophy Type Ii; Lattice Corneal Dystrophy, Gelsolin Type
Registry Numbers: 0
Heading Mapped to: *Corneal Dystrophies, Hereditary; *Amyloid Neuropathies, Familial
Frequency: 1
Date of Entry: 2020/10/01
Revision Date: 2020/09/30

Lattice Corneal Dystrophy, Type II MeSH Supplementary Concept Data 2025