ID: 18 Disease Name: Meretoja Syndrome Description: Disease Type: Amyloidosis ISA Name: AGel Amyloidosis ICD-10 Classification: Amyloidosis Tissue: Central Nervous System (CNS), Peripheral Nervous System (PNS), Eye, Skin, Smooth Muscles, Skeletal Muscles, Heart, Kidney Cross References http://apps.who.int/classifications/icd10/browse/2016/en#/E85 https://meshb.nlm.nih.gov/record/ui?ui=C537459 https://www.omim.org/entry/105120 https://www.ncbi.nlm.nih.gov/pubmed/2157434 https://www.ncbi.nlm.nih.gov/pubmed/2153578 https://www.ncbi.nlm.nih.gov/pubmed/1338910 https://www.ncbi.nlm.nih.gov/pubmed/2175344 https://www.ncbi.nlm.nih.gov/pubmed/4313418 https://www.ncbi.nlm.nih.gov/pubmed/9547007 Alternative Names: Amyloid cranial neuropathy with lattice corneal dystrophy Amyloidosis 5 Amyloidosis V Amyloidosis due to mutant gelsolin Amyloidosis, Finnish Type Amyloidosis, Meretoja Type Cerebral Amyloid Angiopathy, Gsn-Related Corneal Dystrophy, Lattice Type II Familial Amyloid Polyneuropathy Type IV Familial Amyloidosis, Finnish Type Finnish type amyloidosis Gelsolin-Related Amyloidosis Kymenlaakso Syndrome Lattice Corneal Dystrophy Type II Lattice Corneal Dystrophy, Gelsolin Type Lattice Corneal Dystrophy, Type II Lattice corneal dystrophy associated with familial systemic amyloidosis Lattice dystrophy of the cornea with hereditary generalized amyloidosis Meretoja type amyloidosis Meretoja's syndrome Meretoja syndrome Gelsolin amyloidosis Hereditary amyloidosis, Finnish type Meretoja Type Meretoja's disease Hereditary Gelsolin Amyloidosis (HGA) Familial Amyloid Polyneuropathy, Type IV Familial Amyloid Neuropathy, Finnish Type Finnish Type Familial Amyloid Neuropathy Type IV Familial Amyloid Polyneuropathy Precursor Proteins: P06396 | Gelsolin Co-deposited Proteins: P01009 | Alpha-1-antitrypsin P01024 | Complement C3 P01034 | Cystatin-C P02649 | Apolipoprotein E P02743 | Serum amyloid P-component P02748 | Complement component C9 P62736 | Actin, aortic smooth muscle Link to Amyloidosis: No information available //