Details of Disease

General Information of Disease (ID: DIS8KVEV)

Disease Name Lattice corneal dystrophy
Synonyms lattice corneal dystrophy (disease); lattice corneal dystrophy; familial amyloid neuropathy, Finnish type
Definition Editor note: TODO this class sourced from DO, may contain mistakes; may be confused with Lattice corneal dystrophy type II
Disease Hierarchy
DIS41FDX: Stromal corneal dystrophy
DIS8KVEV: Lattice corneal dystrophy
Disease Identifiers
MONDO ID
MONDO_0004686
MESH ID
D028227
UMLS CUI
C0155127
MedGen ID
56355
HPO ID
HP:0001149
SNOMED CT ID
361199007

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 2 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
TTR TTPOYU7 moderate Biomarker [1]
GSN TTUH7OM Strong Biomarker [2]
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References

1 [Therapeutic strategy for familial amyloid polyneuropathy (FAP)].Rinsho Shinkeigaku. 2009 Nov;49(11):953-5. doi: 10.5692/clinicalneurol.49.953.
2 Amyloidosis and Ocular Involvement: an Overview.Semin Ophthalmol. 2020 Jan 2;35(1):7-26. doi: 10.1080/08820538.2019.1687738. Epub 2019 Dec 12.