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193413001: Leber's amaurosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
297841012 Leber's amaurosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
297842017 CRB - Congenital retinal blindness en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
297843010 Congenital retinal blindness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
577300011 Leber's amaurosis (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2619480010 Leber congenital amaurosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2839261016 Leber amaurosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leber's amaurosis Is a Vision problem false Inferred relationship Some
Leber's amaurosis Is a Disorder of posterior segment of eye false Inferred relationship Some
Leber's amaurosis Finding site Retinal structure false Inferred relationship Some
Leber's amaurosis Is a Congenital anomaly of eye false Inferred relationship Some
Leber's amaurosis Is a Retinal disorder false Inferred relationship Some
Leber's amaurosis Occurrence Congenital false Inferred relationship Some
Leber's amaurosis Is a Congenital disease (disorder) true Inferred relationship Some
Leber's amaurosis Occurrence Congenital false Inferred relationship Some 1
Leber's amaurosis Finding site Retinal structure false Inferred relationship Some 1
Leber's amaurosis Is a Hereditary retinal dystrophy true Inferred relationship Some
Leber's amaurosis Associated morphology Dystrophy true Inferred relationship Some 2
Leber's amaurosis Occurrence Congenital true Inferred relationship Some 2
Leber's amaurosis Finding site Retinal structure true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
X-linked intellectual disability, limb spasticity, retinal dystrophy, arginine vasopressin deficiency (disorder) Is a True Leber's amaurosis Inferred relationship Some
Spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual disability, Leber congenital amaurosis syndrome (disorder) Is a True Leber's amaurosis Inferred relationship Some

This concept is not in any reference sets

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