Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2020. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 477683013 | Familial amyloid neuropathy, Finnish type | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module | 
| 477684019 | Finnish type amyloidosis | en | Synonym | Inactive | Entire term case sensitive | SNOMED CT core module | 
| 477685018 | Amyloid cranial neuropathy with lattice corneal dystrophy | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module | 
| 477686017 | Familial amyloid polyneuropathy type V | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module | 
| 477687014 | Amyloid corneal dystrophy | en | Synonym | Inactive | Only initial character case insensitive | SNOMED CT core module | 
| 477688016 | Finland type amyloidosis | en | Synonym | Inactive | Entire term case sensitive | SNOMED CT core module | 
| 477689012 | Meretoja type amyloidosis | en | Synonym | Inactive | Entire term case sensitive | SNOMED CT core module | 
| 743196010 | Lattice corneal dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 2693123015 | Lattice corneal dystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Lattice corneal dystrophy Type I | Is a | True | Lattice corneal dystrophy | Inferred relationship | Existential restriction modifier | |
| Lattice corneal dystrophy Type II | Is a | False | Lattice corneal dystrophy | Inferred relationship | Existential restriction modifier | |
| Lattice corneal dystrophy Type III | Is a | False | Lattice corneal dystrophy | Inferred relationship | Existential restriction modifier | |
| Lattice dystrophy of substantia propria of cornea of bilateral eyes | Is a | True | Lattice corneal dystrophy | Inferred relationship | Existential restriction modifier | 
This concept is not in any reference sets