loading...| Preferred Name |
Meretoja syndrome |
|
| Synonyms |
Amyloidosis 5 Meretoja's syndrome Lattice corneal dystrophy associated with familial systemic amyloidosis Amyloidosis V Amyloidosis, Finnish Type Cerebral Amyloid Angiopathy, Gsn-Related Amyloid cranial neuropathy with lattice corneal dystrophy Lattice dystrophy of the cornea with hereditary generalized amyloidosis Amyloidosis due to mutant gelsolin Finnish type amyloidosis Amyloidosis, Meretoja Type Meretoja type amyloidosis |
|
| ID |
http://purl.bioontology.org/ontology/MESH/C537459 |
|
| altLabel |
Amyloidosis 5 Meretoja's syndrome Lattice corneal dystrophy associated with familial systemic amyloidosis Amyloidosis V Amyloidosis, Finnish Type Cerebral Amyloid Angiopathy, Gsn-Related Amyloid cranial neuropathy with lattice corneal dystrophy Lattice dystrophy of the cornea with hereditary generalized amyloidosis Amyloidosis due to mutant gelsolin Finnish type amyloidosis Amyloidosis, Meretoja Type Meretoja type amyloidosis |
|
| cui |
C1622345 C2751493 |
|
| HM |
D000686 D003317 |
|
| Inverse of RB |
0 |
|
| Mapped to | ||
| MDA |
20100825 |
|
| MeSH Frequency |
23 |
|
| MMR |
20200929 |
|
| notation |
C537459 |
|
| prefLabel |
Meretoja syndrome |
|
| SC |
3 |
|
| Scope Statement |
PROM mutation in gelsolin |
|
| TERMUI |
T742670 T742671 T744213 T742668 T744212 T744215 T802487 T744214 T802489 T744211 T802488 T742669 T811064 |
|
| TH |
OMIM (2013) GHR (2014) ORD (2010) |
|
| tui |
T047 |