FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

719296002: posterieure amorfe corneadystrofie (aandoening)


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

Descriptions:

Id Description Lang Type Status Case? Module
3315891010 Posterior amorphous corneal dystrophy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315892015 Posterior amorphous corneal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315893013 Posterior amorphous stromal dystrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6575581000146118 posterieure amorfe corneadystrofie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6575591000146116 posterieure amorfe corneadystrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3315894019 A very rare form of stromal corneal dystrophy with characteristics of irregular amorphous sheet-like opacities in the posterior corneal stroma and in the Descemet membrane along with mildly impaired vision. Prevalence of this form of corneal dystrophy is not known. To date cases have been reported primarily in the USA. Patients usually develop corneal abnormalities in infancy or childhood. The condition is non-progressive or slowly progressive. Unlike other corneal dystrophies, non-corneal manifestations have been observed and include abnormalities of the iris including iridocorneal adhesions, corectopia, and pseudopolycoria. An autosomal dominant pattern of inheritance has been reported. 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
Posterior amorphous corneal dystrophy (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Posterior amorphous corneal dystrophy (disorder) Is a Hereditary corneal dystrophy true Inferred relationship Some
Posterior amorphous corneal dystrophy (disorder) Is a Stromal corneal dystrophy true Inferred relationship Some
Posterior amorphous corneal dystrophy (disorder) Is a Connective tissue hereditary disorder (disorder) true Inferred relationship Some
Posterior amorphous corneal dystrophy (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Posterior amorphous corneal dystrophy (disorder) Finding site Structure of substantia propria of cornea true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

Back to Start