Lattice Corneal Dystrophy, Type II

Preferred Label : Lattice Corneal Dystrophy, Type II;

MeSH synonym : Lattice Corneal Dystrophy Type Ii; Lattice Corneal Dystrophy, Gelsolin Type; Familial Amyloidosis, Finnish Type; Gelsolin-Related Amyloidosis; Kymenlaakso Syndrome; Corneal Dystrophy, Lattice Type II; Familial Amyloid Polyneuropathy Type Iv;

Détails

Origin ID

C000657784;

UMLS CUI

C5400732;

False automatic mappings
- AGel amyloidosis [ORDO Disease]
MeSH term(s) associated for indexing
- amyloid neuropathies, familial [MeSH Descriptor]
- corneal dystrophies, hereditary [MeSH Descriptor]
Record concept(s)
- lattice corneal dystrophy, type II [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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