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723582004: Subepithelial mucinous corneal dystrophy (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3425174013 Subepithelial mucinous corneal dystrophy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3425175014 Subepithelial mucinous corneal dystrophy en Synonym Active Case insensitive SNOMED CT core
3425176010 A very rare form of superficial corneal dystrophy with characteristics of frequent recurrent corneal erosions in the first decade of life and progressive loss of vision. The condition has only been reported in one single family. Painful episodes of recurrent corneal erosions occur in the first decade of life but decrease during adolescence. Later in life, patients are reported to develop subepithelial opacities and a corneal haze. The disease eventually progresses over time leading to corneal opacities and loss of vision. The gene related to this disease has not been mapped to a particular chromosomal locus. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Subepithelial mucinous corneal dystrophy Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Subepithelial mucinous corneal dystrophy Is a Hereditary corneal dystrophy true Inferred relationship Some
Subepithelial mucinous corneal dystrophy Associated morphology Dystrophy true Inferred relationship Some 1
Subepithelial mucinous corneal dystrophy Finding site Corneal structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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