U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from MedGen

Meretoja syndrome [Supplementary Concept]

PROM mutation in gelsolin

Date introduced: August 25, 2010

MeSH Unique ID: C537459

Heading Mapped to:

Entry Terms:

  • Amyloid cranial neuropathy with lattice corneal dystrophy
  • Amyloidosis 5
  • Amyloidosis due to mutant gelsolin
  • Amyloidosis V
  • Amyloidosis, Finnish Type
  • Amyloidosis, Meretoja Type
  • 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
  • Cerebral Amyloid Angiopathy, Gsn-Related

Supplemental Content

Loading ...