PMO Precision Medicine Ontology

Last uploaded: December 16, 2020
Preferred Name

Lattice Corneal Dystrophy
Synonyms
Definitions

The presence of fine, branching linear opacities in Bowman's layer in the central area that may spread to the periphery in the clinical course. The deep corneal stroma may be involved but the process does not reach Descemet's membrane. Recurrent corneal erosion may occur. Histologic examination reveals amyloid deposits in the collagen fibers of the cornea.

ID

http://www.phoc.org.cn/pmo/class/PMO_00006494

Database_Cross_Reference

HPO:HP:0001149

SNOMEDCT_US:231932008

SNOMEDCT_US:361199007

MTH:NOCODE

MDR:10024039

MSH:D028227

SNOMEDCT_US:193835001

SNOMEDCT_US:1192004

ICD10CM:H18.54

SNMI:D6-94556

OMIM:MTHU036631

RCD:F4B54

SNMI:DA-75412

SNM:M-55110

MEDCIN:36703

ICD9CM:371.54

SNOMEDCT_US:419398009

SNOMEDCT_US:71041007

Definition

The presence of fine, branching linear opacities in Bowman's layer in the central area that may spread to the periphery in the clinical course. The deep corneal stroma may be involved but the process does not reach Descemet's membrane. Recurrent corneal erosion may occur. Histologic examination reveals amyloid deposits in the collagen fibers of the cornea.

label

Lattice Corneal Dystrophy

MCID

MC00060511

PMOID

PMO:00006494

prefixIRI

pmo:PMO_00006494

prefLabel

Lattice Corneal Dystrophy

Synonym

Familial Amyloid Polyneuropathy, Type V

Type V Familial Amyloid Polyneuropathy

Finland type amyloidosis

Lattice corneal dystrophy (disorder)

Lattice cornea dystrophy

Amyloid cranial neuropathy with lattice corneal dystrophy

Lattice corneal dystrophy [Ambiguous]

Familial amyloid neuropathy, Finnish type (disorder)

Amyloid corneal dystrophy

Familial amyloid polyneuropathy type V

Lattice dystrophy of cornea

Amyl cran corneal dystr

Lattice corneal dystrophy

Finnish Type Familial Amyloid Neuropathy

Biber haab dimmer dystrophy

lattice corneal dystrophy (diagnosis)

Finnish type amyloidosis

Familial amyloid neuropathy, Finnish type

Famil amyloid polyneuropath V

Tree Number

T3.18.1.7.4.1.8

subClassOf

http://www.phoc.org.cn/pmo/class/PMO_00006490

Delete Subject Author Type Created
No notes to display