Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

AMYLOIDOSIS, FINNISH TYPE

Synonyms

CEREBRAL AMYLOID ANGIOPATHY, GSN-RELATED

ID

http://purl.bioontology.org/ontology/OMIM/105120

altLabel

CEREBRAL AMYLOID ANGIOPATHY, GSN-RELATED

CORNEAL DYSTROPHY, LATTICE TYPE II

AMYLOIDOSIS, MERETOJA TYPE

AMYLOID CRANIAL NEUROPATHY WITH LATTICE CORNEAL DYSTROPHY

AMYLOIDOSIS DUE TO MUTANT GELSOLIN

AMYLOIDOSIS V

LATTICE CORNEAL DYSTROPHY, TYPE II

LCD2

cui

C1622345

C1628319

C2751493

Gene Locus

9q34

Gene Symbol

GSN

MIMTYPEMEANING

Phenotype description, molecular basis known.

notation

105120

OMIM Entry Type

3

OMIM MimType Value

pound

prefLabel

AMYLOIDOSIS, FINNISH TYPE

tui

T047

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http://purl.bioontology.org/ontology/MESH/C537459 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C537459 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C537459 Medical Subject Headings CUI