- OMIM ID
-
105120
- OMIM term:
- AMYLOIDOSIS, FINNISH TYPE
- Alternative terms:
-
AMYLOIDOSIS V
AMYLOIDOSIS, MERETOJA TYPE
AMYLOID CRANIAL NEUROPATHY WITH LATTICE CORNEAL DYSTROPHY
AMYLOIDOSIS DUE TO MUTANT GELSOLIN CEREBRAL AMYLOID ANGIOPATHY, GSN-RELATED, INCLUDED
CORNEAL DYSTROPHY, LATTICE TYPE II, INCLUDED; LCD2, INCLUDED
LATTICE CORNEAL DYSTROPHY, TYPE II, INCLUDED
- (∗) Location:
- 9q33.2
- (†) Associated OMIM genes:
- GSN
- (‡) Associated MGI genes:
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