loading...| Preferred Name |
Meretoja syndrome |
| Synonyms |
Lattice corneal dystrophy associated with familial systemic amyloidosis |
| ID |
http://purl.bioontology.org/ontology/MESH/C537459 |
| altLabel |
Lattice corneal dystrophy associated with familial systemic amyloidosis Corneal Dystrophy, Lattice Type II Finnish type amyloidosis Cerebral Amyloid Angiopathy, Gsn-Related Amyloidosis 5 Lattice Corneal Dystrophy, Gelsolin Type Amyloid cranial neuropathy with lattice corneal dystrophy Gelsolin-Related Amyloidosis Kymenlaakso Syndrome Amyloidosis, Finnish Type Familial Amyloid Polyneuropathy Type Iv Meretoja's syndrome Amyloidosis, Meretoja Type Amyloidosis V Meretoja type amyloidosis Familial Amyloidosis, Finnish Type Amyloidosis due to mutant gelsolin Lattice Corneal Dystrophy Type Ii Lattice dystrophy of the cornea with hereditary generalized amyloidosis Lattice Corneal Dystrophy, Type II |
| cui |
C1622345 C1628319 C2751493 |
| HM |
D003317 D000686 |
| Inverse of RB |
0 |
| Mapped to | |
| MDA |
20100825 |
| MeSH Frequency |
14 |
| MMR |
20131024 |
| notation |
C537459 |
| prefLabel |
Meretoja syndrome |
| SC |
3 |
| Scope Statement |
PROM mutation in gelsolin |
| TERMUI |
T744213 T841878 T744211 T841875 T802489 T841879 T802487 T742670 T841877 T811064 T742669 T827729 T841876 T744215 T841880 T802488 T742671 T742668 T827730 T744214 T744212 |
| TH |
ORD (2010) OMIM (2013) GHR (2014) |
| tui |
T047 |