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734026006: geïsoleerde congenitale megalocornea (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3481980019 Isolated congenital megalocornea (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3481981015 Isolated congenital megalocornea en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3481982010 Congenital anterior megalophthalmia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6137101000146119 geïsoleerde congenitale megalocornea nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6137111000146117 geïsoleerde congenitale megalocornea (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6137121000146110 congenitale anterieure megaloftalmie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3481983017 Isolated congenital megalocornea is a genetic, non-syndromic developmental defect of the anterior eye segment. The disease has characteristics of bilateral enlargement of the corneal diameter and a deep anterior eye chamber, without an elevation in intraocular pressure. It can manifest with mild to moderate myopia as well as photophobia and iridodonesis (due to iris hypoplasia). Associated complications include lens dislocation, retinal detachment, presenile cataract development and secondary glaucoma. There is evidence this disease is caused by mutation in the CHRDL1 gene on chromosome Xq23. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Isolated congenital megalocornea (disorder) Is a X-linked hereditary disease false Inferred relationship Some
Isolated congenital megalocornea (disorder) Is a Megalocornea true Inferred relationship Some
Isolated congenital megalocornea (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Isolated congenital megalocornea (disorder) Associated morphology congenitale vergroting false Inferred relationship Some 1
Isolated congenital megalocornea (disorder) Occurrence Congenital true Inferred relationship Some 1
Isolated congenital megalocornea (disorder) Finding site Corneal structure true Inferred relationship Some 1
Isolated congenital megalocornea (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Isolated congenital megalocornea (disorder) Associated morphology Enlargement (morphologic abnormality) true Inferred relationship Some 1
Isolated congenital megalocornea (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Isolated congenital megalocornea (disorder) Is a X-linked recessive hereditary disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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